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International Journal of Nephrology
Volume 2011 (2011), Article ID 527137, 10 pages
Nephronophthisis: A Genetically Diverse Ciliopathy
1Institute of Human Genetics, International Centre for Life, Newcastle University, Central Parkway, Newcastle upon Tyne NE1 3BZ, UK
2Renal Services, Freeman Hospital, The Newcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle Upon Tyne NE7 7DN, UK
Received 14 February 2011; Accepted 28 February 2011
Academic Editor: Franz Schaefer
Copyright © 2011 Roslyn J. Simms et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Nephronophthisis (NPHP) is an autosomal recessive cystic kidney disease and a leading genetic cause of established renal failure (ERF) in children and young adults. Early presenting symptoms in children with NPHP include polyuria, nocturia, or secondary enuresis, pointing to a urinary concentrating defect. Renal ultrasound typically shows normal kidney size with increased echogenicity and corticomedullary cysts. Importantly, NPHP is associated with extra renal manifestations in 10–15% of patients. The most frequent extrarenal association is retinal degeneration, leading to blindness. Increasingly, molecular genetic testing is being utilised to diagnose NPHP and avoid the need for a renal biopsy. In this paper, we discuss the latest understanding in the molecular and cellular pathogenesis of NPHP. We suggest an appropriate clinical management plan and screening programme for individuals with NPHP and their families.
Nephronophthisis (NPHP) is an autosomal recessive cystic kidney disease and a leading genetic cause of established renal failure (ERF) in children and young adults . NPHP literally means “disappearance of nephrons,” which alludes to its histopathology, with interstitial fibrosis and corticomedullary cysts replacing normal renal tissue. The median age of an affected child with ERF is 13 years . The incidence of NPHP varies worldwide; it was previously identified to range from 1 in 50,000 to 1 in 900,000 [3–5]; however, these figures are likely to underrepresent the true frequency, since molecular testing has diagnosed NPHP in adults presenting with advanced chronic kidney disease (CKD) [6, 7]. The prevalence of NPHP amongst the paediatric population with ERF is 5% in the USA  and 6.5% in the UK [8, 9].
Early presenting symptoms in children with NPHP usually develop at around 6 years of age and include polyuria, nocturia or secondary enuresis, polydipsia, and lethargy (secondary to anaemia) . These features are a consequence of salt wasting and an inability to concentrate urine (<400 mosm/kg early morning urine), implicating dysfunction of the renal cortical collecting duct . Renal ultrasound identifies normal or reduced kidney size, with increased echogenicity and corticomedullary cysts . There is a less common infantile variant of NPHP in which children reach ERF by 3 years of age and have enlarged cystic kidneys on renal ultrasound . Infantile NPHP is distinct from autosomal recessive polycystic kidney disease (ARPKD). There is a diffuse distribution of cysts within the kidneys of children with ARPKD, and it is more often associated with liver cysts and fibrosis . A diagnostic renal biopsy of NPHP reveals a characteristic triad of tubular basement membrane disruption, tubulointerstitial nephropathy/fibrosis, and corticomedullary cysts [4, 14]. Increasingly, molecular genetic testing  is being utilised to diagnose NPHP and avoid the need for a renal biopsy .
NPHP is associated with extra renal manifestations in 10–15% of patients . The most frequent anomaly is retinal degeneration; other associated features and disorders include cerebellar vermis hypoplasia (Joubert Syndrome (JS)), occipital encephalocele (Meckel-Gruber syndrome (MKS)), hepatic fibrosis, situs inversus, bronchiectasis, and skeletal defects . In addition to this apparent variability in the spectrum and severity of phenotype, NPHP is genetically heterogenous. To date mutations have been identified in 13 genes (Table 1) which collectively account for approximately 30% of patients . The protein products of all of these genes localise on primary cilia and related structures (basal bodies, centrosomes), resulting in a unifying hypothesis that cystic kidney diseases are ciliopathies . In this paper, we will discuss the latest understanding in the molecular and cellular pathogenesis of NPHP and suggest an appropriate management plan/screening programme for individuals and their families, particularly in view of the considerable clinical heterogeneity.
2. Molecular and Genetic Pathogenesis
NPHP is a recessive monogenic disorder , meaning that two mutations (homozygous or compound heterozygous) in a single gene are sufficient to cause disease . Thirteen genes have been identified in affected families with NPHP (Table 1), and these genes currently allow 30% of patients with NPHP to be “solved” in terms of a molecular diagnosis. These genes have been identified using positional cloning strategies and homozygosity mapping in consanguineous families . Subsequent localisation of all these encoded proteins, termed “nephrocystins,” to the primary cilium/basal body led to recognition of NPHP as a ciliopathy . Primary cilia are highly conserved, microtubule-based hair-like structures which extend from the apical surface of almost every epithelial cell. They function in order to detect extracellular cues and mediate cellular signalling pathways (discussed below) . Ciliary genes are currently recognised as attractive candidates to evaluate when attempting to define the molecular cause of NPHP in the presently undiagnosed 70% of patients. With this in mind, combined homozygosity mapping, ciliopathy candidate exome capture, and parallel sequencing have recently been performed resulting in the successful identification of pathological mutations in the gene, serologically defined colon cancer antigen 8 (SDCCAG8), in families with NPHP . SDCCAG8 is synonymous with NPHP10. Also recently, the targeted screen of the ciliary gene TTC21B revealed that its protein product, IFT139, is essential for retrograde intraflagellar transport. IFT139 interacts with ciliopathy proteins BBS4 and BBS8, and pathogenic mutations in TTC21B were identified in patients with NPHP and more severe related ciliopathies .
Although the majority of currently known NPHP genes produce proteins which localise to primary cilia/basal bodies/centrosomes, recent identification of an NPHP-like locus in two affected families suggests that NPHP genes may not be exclusively ciliary . Genome-wide homozygosity mapping identified pathogenic mutations in X-prolyl aminopeptidase 3 (XPNPEP3), or NPHPL1 (NPHP like 1 gene), of which the protein product localises to mitochondria . Although not currently identified in the primary cilium, XPNPEP3 may influence cilia function through enzymatic cleavage of associated ciliary proteins .
Whilst homozygous mutations in the NPHP genes can cause isolated NPHP, mutations in the same gene can be pleiotropic inducing a spectrum and variable severity of phenotypes. Similarly, it would appear logical that the type of mutation may influence the phenotype. For example, a missense mutation may cause isolated NPHP or Senior-Loken syndrome (SLS, retinitis pigmentosa), whilst a truncating mutation could cause MKS. Recently the effect of different mutations in NPHP6 on clinical presentation has been eloquently reviewed . Furthermore, some NPHP genes are more likely to be associated with certain extrarenal features. The concept of “modifier genes” has been recognised in patients with the related ciliopathy, Bardet-Biedl syndrome (BBS), where pathogenic mutations in more than one gene have been detected, implicating a role for oligogenicity . Oligogenicity or triallelism, whereby a mutation in a third allele may exert an epistatic effect and modify the phenotype, has been described in NPHP . A brief description of each of the NPHP genes, their encoded nephrocystin proteins, and any interacting protein partners is given below.
2.1. NPHP1 and Nephrocystin-1
NPHP1 was the first NPHP gene identified and accounts for the majority (20–25%) of known cases of isolated NPHP [23, 24]. Recently adults presenting with signs of NPHP and ERF in two generations of a Turkish family with no known consanguinity suggested a diagnosis of a dominant cystic kidney disease such as medullary cystic kidney disease (MCKD) or perhaps a novel variant of dominant NPHP . However, identification of homozygous mutations in NPHP1 in all affected family members revealed a pseudodominant inheritance of unknown cause as a consequence of unidentified consanguineous relationships. The increased age at presentation with ERF is atypical and is hypothesised to be a consequence of currently unknown modifier genes . NPHP1 mutations can also cause retinal and cerebellar phenotypes leading to SLS and JS. Oligogenicity has been reported in families with NPHP, where mutations in both NPHP1 and NPHP3, NPHP1 and NPHP4 , and NPHP1 and the ciliopathy gene Abelson helper integration site-1 (AHI1, the most frequently mutated gene in JS ) have been detected . Mutations in both NPHP1 and NPHP6 have been identified in patients with NPHP-related ciliopathies including SLS and JS . This evidence of genetic interaction, known protein-protein interactions between various nephrocystins, combined with an awareness of other ciliary proteins such as BBSome functioning as a complex , makes it highly likely that several of the nephrocystins form a functional supramolecular complex within cells [17, 20]. Nephrocystin-1 localises at cell-cell contacts including tight junctions, adherens junctions, and focal adhesions [42, 43]. Nephrocystin-1 has also been identified at the transition zone/base of the primary cilium . Nephrocystin-1 interacts with various other proteins important in maintaining the cellular scaffolding or cytoskeleton including jouberin , ack1 , filamin A and B, tensin (actin binding), β-tubulin (microtubule structure), and protein tyrosine kinase 2B (PTK2B) .
2.2. NPHP2/INVS and Inversin
Mutations in NPHP2 are distinct because they cause infantile NPHP, characterised by an earlier presentation of ERF (at approximately 3 years of age), with enlarged kidneys on ultrasound. Additional clinical features include cardiac anomalies (situs inversus and ventricular septal defects (VSD)) . Although NPHP2 mutations are a rare cause of NPHP compared to NPHP1, there has been intense research regarding the molecular/cellular pathogenesis of inversin. Inversin is located in the primary cilium and other subcellular sites in a cell-cycle dependent manner . A previous work has suggested that inversin acts as a switch between canonical and non-canonical (planar cell polarity) Wnt signalling . When inversin is lost after NPHP2 mutation, it was proposed that sustained canonical Wnt signalling led to cell proliferation and random oriented cell division . However, recent experiments in the inv mutant mouse model of NPHP showed no difference in canonical Wnt signalling compared to controls . In addition to nephrocystin-1, inversin interacts with calmodulin, catenins, β-tubulin , and anaphase-promoting complex 2 [48, 51].
2.3. NPHP3 and Nephrocystin-3
Mutations in NPHP3 are again a rare cause of isolated NPHP; however, they can cause a broad spectrum of phenotypes as shown in Table 1. Nephrocystin-3 colocalises with nephrocystin-1  and inversin  in primary cilia, adherens junctions, and focal adhesions . The pcy mouse model of NPHP displays cystic kidneys and responded to treatment with aquaretic agents/vasopressin-2-receptor antagonists .
2.4. NPHP4 and Nephrocystin-4/Nephroretinin
Individuals with mutations in NPHP4 most frequently have an associated retinal phenotype . Nephrocystin-4 colocalises and interacts with nephrocystins 1, 3 and inversin in primary cilia and associated appendages, adherens junctions, and focal adhesions [20, 27]. Nephrocystin-4 also interacts with nephrocystin-8 [55, 56], α-tubulin, breast cancer antioestrogen resistance 1 (BCAR1), PTK2B , and the tight junction proteins PALS1/PATJ/Crb3 which are required for epithelial morphogenesis .
2.5. NPHP5/IQCB1 and Nephrocystin-5
NPHP5 mutations are associated with early onset retinal degeneration, SLS . Nephrocystin-5 contains two IQ calmodulin binding sites; the significance of its interaction with calmodulin is unclear. It colocalises with nephrocystin-1 and nehrocystin-4 in the primary cilium, adherens junctions, and focal adhesions  and interacts with nephrocystin-6 [30, 58]. Nephrocystin-5 also complexes with the retinal ciliopathy gene retinitis pigmentosa GTPase regulator (RPGR) , explaining the frequent retinal phenotype.
2.6. NPHP6/CEP290 and Nephrocystin-6
Mutations in NPHP6 cause a full spectrum of extrarenal features with no apparent genotype-phenotype correlation . It is the commonest genetic cause (21%) of isolated congenital retinal degeneration, Leber’s congenital amaurosis (LCA) . It was suggested that oligogenicity and the effect of modifier genes may account for some of the pleiotropy. Oligogenicity has been described in patients with homozygous NPHP6 mutations and an additional heterozygous mutation in: NPHP4 resulting in NPHP  or SLS , NPHP11 causing BBS or MKS , and AHI1 causing JS . Oligogenicity has also been identified in patients with SLS and JS as a consequence of a homozygous mutation in NPHP1 and heterozygous mutation in NPHP6 . NPHP6 interacts with and modulates the transcription factor ATF4, involved in cAMP-dependent renal cyst formation . In addition to nephrocystin-5 , another protein interaction partner of nephrocystin-6 is coiled-coil and C2 domain protein (CC2D2A) . In zebrafish models of combined NPHP6 and CC2D2A knockdown, there is synergy of the renal cystic phenotype, suggesting an epistatic, disease-modifying effect . CC2D2A mutations cause JS and MKS ; however, they have not been identified in patients with isolated NPHP [15, 61].
2.7. NPHP7/GLIS2 and GLIS2
NPHP7 is a rare cause of isolated NPHP ; its protein product is a Kruppel-like zinc-finger transcription factor, Gli-similar protein 2, which localises to the primary cilium and nucleus . Interestingly, a Glis2 knockout mouse model showed an upregulation of genes promoting epithelial-to-mesenchymal transition and histological features of NPHP including fibrosis . This correlation of nephrocystin-7 with GLI transcription factors links the pathogenesis of NPHP to the Hedgehog (Hh) signalling pathway, which is essential for controlling tissue maintenance .
2.8. NPHP8/RPGRIP1L and RPGRIP1L
NPHP8 mutations more frequently cause extrarenal manifestations such as cerebello-oculo-renal syndromes, JS [32, 56], and MKS  than isolated NPHP. There appears to be some genotype-phenotype correlation with missense mutations causing LCA , whilst truncating mutations cause the more severe disorder MKS . RPGRIP1L colocalises with nephrocystin-4 and nephrocystin-6 at basal bodies and centrosomes . RPGRIP1L interacts with nephrocystin-1 and nephrocystin-4 .
2.9. NPHP9/NEK8 and NEK8
NPHP9 mutations are a rare cause of both infantile and noninfantile NPHP . Oligogenicity has been identified with a pathogenic homozygous mutation in NPHP5 and heterozygous NPHP9 mutation, which may behave as a modifying gene, in an individual with SLS . In some patients with heterozygous NPHP9 mutations, a second recessive mutation has not been identified. Its protein product, never in mitosis A-related kinase 8 (NEK8), colocalises with various nephrocystins in primary cilia, basal bodies, and centrosomes and appears to be important in regulating the cell cycle . NEK8 has been shown to interact with polycystin-2 (autosomal dominant polycystic kidney disease (ADPKD) protein), to regulate its expression and phosphorylation . NEK8 may thus function in a protein complex with polycystin 1 and 2.
2.10. NPHP10/SDCCAG8 and SDCCAG8
SDCCAG8 was recently identified as NPHP10 by homozygosity mapping, ciliopathy candidate exome capture, and parallel sequencing . Twelve mutations were identified in ten families with NPHP-related ciliopathies, in particular SLS and BBS. Homozygous SDCCAG8 mutations account for 3.3% of cases of SLS. Its protein product, serologically defined colon cancer antigen 8 (SDCCAG8), colocalises at centrosomes and cell-cell junctions with nephrocystin-5. SDCCAG8 and nephrocystin-5 colocalise in the transition zone of photoreceptors which is likely of functional significance and correlates with the phenotype of SLS. SDCCAG8 also colocalises with the retinal ciliopathy proteins RPGRIP and RP1. SDCCAG8 interacts directly with the protein oral-facial-digital syndrome 1 (OFD1) , although the functional significance of this is currently not clear, it is clearly of interest, as recessive mutations in OFD1 are an X-linked cause of the NPHP-related ciliopathy JS .
2.11. NPHP11/TMEM67/MKS3 and TMEM67
Mutations in NPHP11 are pleiotropic, having been identified in patients with NPHP and liver fibrosis, extending to patients with related ciliopathies including JS, MKS , and COACH syndrome (cerebellar vermis hypoplasia, oligophrenia (developmental delay), ataxia, coloboma, and hypotonia) . Whilst oligogenicitiy has not been described, a patient with JS and an isolated heterozygous NPHP11 mutation has been identified , suggesting that triallelism and the role of NPHP11 as a modifier gene is possible. Transmembrane protein 67 (TMEM67) or meckelin localises to the membrane of primary cilia and diffusely at basal and basolateral cell surfaces . TMEM67 interacts with several proteins including nesprin 2 , MKS1 , and TMEM216  which are important in maintaining cellular structure and mitigating centrosome migration, which is essential for ciliogenesis.
2.12. NPHPL1/XPNPEP3 and XPNPEP3
NPHP-like 1 gene (NPHPL1) was recently identified in two consanguineous families with NPHP by genome-wide homozygosity mapping . Additional extrarenal manifestations include cardiomyopathy and seizures. This is a novel discovery because it is the first NPHP gene identified whose protein product, X-propyl aminopeptidase 3 (XPNPEP3), does not localise to primary cilia, basal bodies, or centrosomes . Instead, XPNPEP3 localises in mitochondria; however, it has been hypothesised that this enzyme may be able to interfere with cilia function by cleaving certain cilial proteins [17, 35].
2.13. TTC21B and IFT139
Mutations in TTC21B have recently been identified in families with isolated NPHP and extrarenal manifestations including the ciliopathy, Jeune asphyxiating thoracic dystrophy (JATD) . Interestingly, both causal mutations (homozygous or compound heterozygous) and modifier mutations (heterozygous) in TTC21B were identified in affected individuals. Oligogenicity was identified between TTC21B and several other ciliopathy genes. With regard to NPHP, triallelism was identified in a Turkish family with mutations in both TTC21B and NPHP4. The protein product of TTC21B is a retrograde intraflagellar transport protein IFT139, found in the primary cilium, and is essential for ciliary function.
3. Oligogenicity and Modifier Genes
Oligogenicity has been described above for NPHP1, NPHP5, NPHP6, NPHP8, NPHP9, NPHP11, and TTC21B. It has been hypothesised that oligogenicity may help to account for the intrafamilial variation in age of onset of ERF and severity of clinical features . Current evidence fails to consistently identify a correlation between genotype and phenotype , therefore mutation analysis is required to identify the molecular cause. Making a molecular diagnosis often involves expensive and time-consuming mutation analysis. However, the results may be important when managing patients, to guide appropriate screening for potentially associated complications of the retina, cerebellum, liver and lungs. Understanding the natural history of NPHP and associated complications will hopefully improve following completion of the current clinical trial ongoing in France, which is evaluating the evolution of NPHP and related extrarenal manifestations in children (over 7 years of age) with a confirmed diagnosis of NPHP1–8 (excluding NPHP7) (see http://clinicaltrials.gov/ct2/show/NCT01022957?term=nephronophthisis&rank=1). The results of this study may facilitate understanding in characterising genotype/phenotype associations. Although NPHP-related ciliopathies are heterogenic disorders, the true frequency of oligogenicity remains uncertain. It is however interesting that mutation analysis of 18 NPHP associated ciliopathy disease genes (including 12 NPHP genes, SDCCAG8 was not included) in 120 patients with NPHP and related ciliopathies, using DNA pooling and next generation sequencing, recently failed to identify any evidence of oligogenicity . Remarkably, in 75% of patients in this cohort, no mutations were detected in the known candidate NPHP genes .
Since the molecular cause of NPHP remains unidentified in 70–75% of cases, it is anticipated that additional NPHP genes will be discovered. Whilst genes involved in the structure and function of the primary cilium are logical candidates to consider, indeed this approach has resulted in the recent successful identification of TTC21B , it is interesting that “noncilial” causal genes such as XPNPEP3  are now being identified. Additionally, genes implicated in maintaining the cell cytoskeleton and cellular junctions are likely involved. Whilst identifying causal genes is fundamental to determine the pathogenesis of NPHP, it is the tip of the iceberg and we need to understand the functional consequences of such mutations within tissues. We will now discuss current hypotheses for the cellular pathophysiology of NPHP.
4. Cystic Kidney Disease as a Ciliopathy
In 2005, realisation that polycystin-1 and polycystin-2 (protein products of ADPKD genes PC1 and PC2) and the discovered nephrocystins (NPHP1–5) were all expressed in the primary cilium, basal body, and centrosomes led to consideration of the term “ciliopathy” as a unifying theory for cystic kidney disease . A few years earlier, the concept of a ciliopathy, a disorder in which abnormal structure or function of cilia/centrosomes is associated with defective proteins encoded by mutated genes, was attributed to the multisystem disorder BBS . In the intervening years, the primary cilium  had been extensively studied. Primary cilia are composed of an axoneme containing nine microtubular doublets which extend by a process of intraflagellar transport (IFT) and mediate the trafficking of signals between the extra- and intracellular environments . Cilia are considered to be involved in mechanosensation of urinary flow in the renal tubules .
Normally, in healthy kidneys, the renal cortical collecting duct (CCD) concentrates urine by responding to vasopressin, which binds to vasopressin-2 receptors (V2R). V2R are coupled to adenylyl cyclase resulting in increased intracellular cyclic AMP (cAMP), leading to phosphorylation of aquaporin-2 water channels (AQP2), which mediate water reabsorption . In NPHP, inability to concentrate urine is the earliest clinical feature and is unresponsive to desmopressin therapy . In animal models of NPHP, vasopressin levels are elevated and thought to contribute to cystogenesis by upregulating cell proliferation . Identification of V2R in the primary cilium of renal epithelial cells  is consistent with the theory of cystic kidney diseases as ciliopathies. This also emphasises the importance of the primary cilium in water reabsorption which has recently been eloquently investigated in patients and renal epithelial cell culture models of the related ciliopathy BBS . Understanding the pathogenesis of this urine concentration defect should help explain the success of vasopressin receptor antagonists in animal models of NPHP, where they induced a reduction in cAMP levels and caused regression of cysts .
In NPHP, in response to urinary flow, cilia are considered to alter expression of inversin and potentially influence Wnt signalling pathways and planar cell polarity [17, 78]. Originally, observations in mouse models established the link between primary cilia and cystic kidney disease: the orpk mouse model of ARPKD with a Tg737 mutation (disrupting the protein polaris) has impaired ciliogenesis and renal cysts .
The extrarenal manifestations of NPHP including retinal degeneration and SLS, usually associated with NPHP5 and NPHP6 mutations, can be explained by ciliary dysfunction. Retinal photoreceptors contain a connecting cilium through which rhodopsin traffics along, mediating photosensation . Both nephrocystin-5 and -6 are expressed in the connecting cilia of retinal photoreceptors and disrupted structure or function of these proteins interferes with rhodopsin transport, leading to retinal degeneration (17, 20).
Through their involvement in various cellular signalling pathways including Hh, calcium, and Wnt, cilia mediate several fundamental processes including cell cycle, proliferation, differentiation, and polarity . Proposed mechanisms for renal cystogenesis include abnormal cell proliferation, fluid secretion, and disorientated cell division leading to cystic expansion rather than longitudinal tubular growth . However, aberrations in the signalling pathways linking cilia to cystogenesis remain incompletely understood, complicated by sometimes contradictory evidence. A recent helpfulreview of mechanisms of NPHP discusses each gene . Here we provide an overview, concentrating on the Wnt signalling pathway.
5. Wnt Signalling and NPHP
Wnt signalling involves several ciliary proteins including PC1, PC2, inversin, nephrocystin-3, jouberin, BBS1, BBS4, BBS6, OFD1, and HNF1β, to regulate cell proliferation and differentiation . It is composed of two pathways: canonical (β-catenin dependent) and noncanonical (or planar cell polarity (PCP)); the functional branch appears to be determined in part by inversin acting as a switch at the base of the primary cilium . Interestingly, both over activation [49, 81] and underactivation  of the canonical Wnt pathway have been identified in animal models of NPHP and JS, suggesting that unbalanced canonical Wnt signalling is damaging and mediates cystogenesis . However, this theory has recently been refuted by studies in the inv mouse model of NPHP, where no change in canonical Wnt signalling was identified between cystic inv mutants and controls .
PCP describes the normal intrinsic organisation of cells in a tissue plane perpendicular to their apicobasal polarity . PCP regulates kidney tubule development or recovery from injury by convergent extension and orientated cell division [78, 84], meaning that cells are spatially orientated and divide along an axis to maintain a constant tubule diameter whilst elongating [78, 85]. Several mouse models of cystic kidney disease provide evidence of aberrant PCP signalling [83, 86]. An excellent, comprehensive review of the role of Wnt signalling in cystic kidney disease has been published recently .
The other signalling pathway with particular relevance to understanding the pathophysiology of NPHP is the Hh pathway. An association with NPHP was realised when Hh effector proteins, GLI transcription factors, were noted to be related to GLIS2, the protein product of NPHP7. Loss of GLIS2 promotes epithelial to mesenchymal translation (EMT), fibrosis and apoptosis, and histological hallmarks of NPHP . Thus although NPHP7 is a rare cause of NPHP, its discovery has contributed important understanding to the signalling pathways involved.
6. Clinical Management of NPHP
6.1. Diagnosis and Investigations
In order to establish a clinical diagnosis of NPHP, a detailed history, clinical examination, including looking for extrarenal associations (abnormal eye movements, retinopathy, ataxia, polydactyly, and cardiac malformations) is required. A detailed family history must be taken both to facilitate diagnosis and to highlight other individuals who should be invited for review. Appropriate investigations include renal and liver function tests; urine concentration ability, renal and hepatic ultrasound, cerebral imaging if clinically indicated, and referral to an ophthalmologist (Figure 1) . After genetic counselling, blood may be sent for genetic testing (Table 2) to genetic testing organisations (e.g., http://www.ukgtn.nhs.uk/ or http://www.eurogentest.org/) to seek a molecular diagnosis. Regular review is required to appropriately manage CKD/ERF, and individuals with extrarenal manifestations should be referred to appropriate colleagues and are ideally best managed in specialist clinics.
Presently there is no cure for NPHP and related ciliopathies. Clinicians must focus on optimising the delivery of renal replacement therapy, ideally with renal transplantation where possible. However with a growing understanding of the pathophysiology of NPHP, the future is more hopeful. In recent years various drugs including vasopressin receptor antagonists , mTOR inhibitors (mammalian target of rapamycin) , triptolide  and roscovitine (cyclin-dependent kinase inhibitor)  have been shown to be effective in reducing renal cysts in animal models of NPHP and ADPKD. Many of these drugs are currently or have recently been involved in clinical trials in adult patients. Furthermore, large numbers of compounds which could be potential therapies are being screened in zebrafish  models of ciliopathies.
Understanding of the molecular genetics of NPHP has advanced considerably over the last few years. We are increasingly aware of the heterogeneity, the pleiotropic nature of mutations, and oligogenicity, all of which contribute to the complexity of NPHP. Identification of further NPHP genes, many of which may be “ciliary,” is warranted to provide further clues to its pathogenesis. This will require international multidisciplinary collaboration to sequence patient cohorts with no current molecular diagnosis and to screen candidate genes in animal and cell models. Acknowledgement that the genetic cause is unknown in 70% of NPHP cases, combined with awareness that a mitochondrial gene, XPNPEP3, has recently been identified to cause an NPHP-like phenotype, may encourage us to consider other nonciliary candidates, such as genes involved in cell-cell contacts and the cytoskeleton. Ultimately understanding the physiological outcomes at a protein and cellular level should facilitate identifying and developing novel therapeutic targets for affected patients.
The authors are extremely grateful to Kidney Research UK and the Medical Research Council (Training Fellowship to R. J. Simms). They also acknowledge support from Newcastle Hospitals Healthcare Charity (support for A. M. Hynes), the Kids Kidney Research Fund (support for L. Eley), and GlaxoSmithKline (Clinician Scientist Fellowship to J. A. Sayer).
- F. Hildebrandt and W. Zhou, “Nephronophthisis-associated ciliopathies,” Journal of the American Society of Nephrology, vol. 18, no. 6, pp. 1855–1871, 2007.
- F. Hildebrandt, M. Attanasio, and E. Otto, “Nephronophthisis: disease mechanisms of a ciliopathy,” Journal of the American Society of Nephrology, vol. 20, no. 1, pp. 23–35, 2009.
- D. E. Potter, M. A. Holliday, C. F. Piel, N. J. Feduska, F. O. Belzer, and O. Salvatierra Jr., “Treatment of end-stage renal disease in children: a 15-year experience,” Kidney International, vol. 18, no. 1, pp. 103–109, 1980.
- R. Waldherr, T. Lennert, H. P. Weber, H. J. Födisch, and K. Schärer, “The nephronophthisis complex. A clinicopathologic study in children,” Virchows Archiv A Pathological Anatomy and Histology, vol. 394, no. 3, pp. 235–254, 1982.
- S. Ala-Mello, O. Koskimies, J. Rapola, and H. Kääriäinen, “Nephronophthisis in Finland: epidemiology and comparison of genetically classified subgroups,” European Journal of Human Genetics, vol. 7, no. 2, pp. 205–211, 1999.
- G. Bollée, F. Fakhouri, A. Karras et al., “Nephronophthisis related to homozygous NPHP1 gene deletion as a cause of chronic renal failure in adults,” Nephrology Dialysis Transplantation, vol. 21, no. 9, pp. 2660–2663, 2006.
- J. Hoefele, A. Nayir, M. Chaki, et al., “Pseudodominant inheritance of nephronophthisis caused by a homozygous NPHP1 deletion,” Pediatric Nephrology, vol. 26, no. 6, pp. 967–971, 2011.
- M. Lewis, J. Shaw, C. Reid, J. Evans, N. Webb, and K. Verrier-Jones, “Demography and management of childhood established renal failure in the UK,” Nephrology, Dialysis, Transplantation, vol. 22, supplement 7, pp. vii165–vii175, 2007.
- M. A. Lewis, J. Shaw, M. Sinha, S. Adalat, F. Hussain, and C. Inward, “UK renal registry 11th annual report (December 2008): chapter 13 demography of the UK paediatric renal replacement therapy population,” Nephron—Clinical Practice, vol. 111, supplement 1, pp. c257–c267, 2009.
- S. Ala-Mello, S. M. Kivivuori, K. A. R. Rönnholm, O. Koskimies, and M. A. Siimes, “Mechanism underlying early anaemia in children with familial juvenile nephronophthisis,” Pediatric Nephrology, vol. 10, no. 5, pp. 578–581, 1996.
- R. Krishnan, L. Eley, and J. A. Sayer, “Urinary concentration defects and mechanisms underlying nephronophthisis,” Kidney and Blood Pressure Research, vol. 31, no. 3, pp. 152–162, 2008.
- R. Salomon, S. Saunier, and P. Niaudet, “Nephronophthisis,” Pediatric Nephrology, vol. 24, no. 12, pp. 2333–2344, 2009.
- A. M. Waters and P. L. Beales, “Ciliopathies: an expanding disease spectrum,” Pediatric Nephrology. In press.
- H. U. Zollinger, M. J. Mihatsch, and A. Edefonti, “Nephronophthisis (medullary cystic disease of the kidney). A study using electron microscopy, immunofluorescence, and a review of the morphological findings,” Helvetica Paediatrica Acta, vol. 35, no. 6, pp. 509–530, 1980.
- E. A. Otto, G. Ramaswami, S. Janssen, et al., “Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy,” Journal of Medical Genetics, vol. 48, pp. 105–116, 2011.
- R. J. Simms, L. Eley, and J. A. Sayer, “Nephronophthisis,” European Journal of Human Genetics, vol. 17, no. 4, pp. 406–416, 2009.
- T. W. Hurd and F. Hildebrandt, “Mechanisms of nephronophthisis and related ciliopathies,” Nephron Experimental Nephrology, vol. 118, pp. e9–e14, 2011.
- F. Hildebrandt and E. Otto, “Cilia and centrosomes: a unifying pathogenic concept for cystic kidney disease?” Nature Reviews Genetics, vol. 6, no. 12, pp. 928–940, 2005.
- F. Hildebrandt, “Genetic kidney diseases,” The Lancet, vol. 375, no. 9722, pp. 1287–1295, 2010.
- M. T. Wolf and F. Hildebrandt, “Nephronophthisis,” Pediatric Nephrology, vol. 26, pp. 181–194, 2011.
- E. A. Otto, T. W. Hurd, R. Airik, et al., “Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy,” Nature Genetics, vol. 42, pp. 840–850, 2010.
- E. E. Davis, Q. Zhang, Q. Liu, et al., “TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum,” Nature Genetics, vol. 43, no. 3, pp. 189–196, 2011.
- F. Hildebrandt, E. Otto, C. Rensing et al., “A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1,” Nature Genetics, vol. 17, no. 2, pp. 149–153, 1997.
- S. Saunier, J. Calado, R. Heilig et al., “A novel gene that encodes a protein with a putative src homology 3 domain is a candidate gene for familial juvenile nephronophthisis,” Human Molecular Genetics, vol. 6, no. 13, pp. 2317–2323, 1997.
- E. A. Otto, B. Schermer, T. Obara et al., “Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination,” Nature Genetics, vol. 34, no. 4, pp. 413–420, 2003.
- H. Olbrich, M. Fliegauf, J. Hoefele et al., “Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis,” Nature Genetics, vol. 34, no. 4, pp. 455–459, 2003.
- G. Mollet, R. Salomon, O. Gribouval et al., “The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin,” Nature Genetics, vol. 32, no. 2, pp. 300–305, 2002.
- E. Otto, J. Hoefele, R. Ruf et al., “A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution,” American Journal of Human Genetics, vol. 71, no. 5, pp. 1161–1167, 2002.
- E. A. Otto, B. Loeys, H. Khanna et al., “Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin,” Nature Genetics, vol. 37, no. 3, pp. 282–288, 2005.
- J. A. Sayer, E. A. Otto, J. F. O'Toole et al., “The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4,” Nature Genetics, vol. 38, no. 6, pp. 674–681, 2006.
- M. Attanasio, N. H. Uhlenhaut, V. H. Sousa et al., “Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis,” Nature Genetics, vol. 39, no. 8, pp. 1018–1024, 2007.
- M. T. F. Wolf, S. Saunier, J. F. O'Toole et al., “Mutational analysis of the RPGRIP1L gene in patients with Joubert syndrome and nephronophthisis,” Kidney International, vol. 72, no. 12, pp. 1520–1526, 2007.
- E. A. Otto, M. L. Trapp, U. T. Schultheiss, J. Helou, L. M. Quarmby, and F. Hildebrandt, “NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis,” Journal of the American Society of Nephrology, vol. 19, no. 3, pp. 587–592, 2008.
- E. A. Otto, K. Tory, M. Attanasio et al., “Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11),” Journal of Medical Genetics, vol. 46, no. 10, pp. 663–670, 2009.
- J. F. O'Toole, Y. Liu, E. E. Davis et al., “Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy,” Journal of Clinical Investigation, vol. 120, no. 3, pp. 791–802, 2010.
- F. Coppieters, S. Lefever, B. P. Leroy, et al., “CEP290, a gene with many faces: mutation overview and presentation of CEP290base,” Human Mutation, vol. 31, pp. 1097–1108, 2010.
- J. L. Bandano, J. C. Kim, B. E. Hoskins et al., “Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Beidl patients with two mutations at a second BBS locus,” Human Molecular Genetics, vol. 12, no. 14, pp. 1651–1659, 2003.
- J. Hoefele, M. T. F. Wolf, J. F. O'Toole et al., “Evidence of oligogenic inheritance in nephronophthisis,” Journal of the American Society of Nephrology, vol. 18, no. 10, pp. 2789–2795, 2007.
- B. Utsch, J. A. Sayer, M. Attanasio et al., “Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome,” Pediatric Nephrology, vol. 21, no. 1, pp. 32–35, 2006.
- M. A. Parisi, C. L. Bennett, M. L. Eckert et al., “The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome,” American Journal of Human Genetics, vol. 75, no. 1, pp. 82–91, 2004.
- K. Tory, T. Lacoste, L. Burglen et al., “High NPHP1 and NPHP6 mutation rate in patients with Joubert syndrome and nephronophthisis: potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutations,” Journal of the American Society of Nephrology, vol. 18, no. 5, pp. 1566–1575, 2007.
- J. C. Donaldson, P. J. Dempsey, S. Reddy, A. H. Bouton, R. J. Coffey, and S. K. Hanks, “Crk-associated substrate p130(Cas) interacts with nephrocystin and both proteins localize to cell-cell contacts of polarized epithelial cells,” Experimental Cell Research, vol. 256, no. 1, pp. 168–178, 2000.
- T. Benzing, P. Gerke, K. Höpker, F. Hildebrandt, E. Kim, and G. Walz, “Nephrocystin interacts with Pyk2, p130, and tensin and triggers phosphorylation of Pyk2,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 17, pp. 9784–9789, 2001.
- M. Fliegauf, J. Horvath, C. Von Schnakenburg et al., “Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting cilia,” Journal of the American Society of Nephrology, vol. 17, no. 9, pp. 2424–2433, 2006.
- L. Eley, C. Gabrielides, M. Adams, C. A. Johnson, F. Hildebrandt, and J. A. Sayer, “Jouberin localizes to collecting ducts and interacts with nephrocystin-1,” Kidney International, vol. 74, no. 9, pp. 1139–1149, 2008.
- L. Eley, S. H. Moochhala, R. Simms, F. Hildebrandt, and J. A. Sayer, “Nephrocystin-1 interacts directly with Ack1 and is expressed in human collecting duct,” Biochemical and Biophysical Research Communications, vol. 371, no. 4, pp. 877–882, 2008.
- M. F. Gagnadoux, J. L. Bacri, M. Broyer, and R. Habib, “Infantile chronic tubulo-interstitial nephritis with cortical microcysts: variant of nephronophthisis or new disease entity?” Pediatric Nephrology, vol. 3, no. 1, pp. 50–55, 1989.
- D. Morgan, L. Eley, J. Sayer et al., “Expression analyses and interaction with the anaphase promoting complex protein Apc2 suggest a role for inversin in primary cilia and involvement in the cell cycle,” Human Molecular Genetics, vol. 11, no. 26, pp. 3345–3350, 2002.
- M. Simons, J. Gloy, A. Ganner et al., “Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways,” Nature Genetics, vol. 37, no. 5, pp. 537–543, 2005.
- N. Sugiyama, T. Tsukiyama, T. P. Yamaguchi, et al., “The canonical Wnt signaling pathway is not involved in renal cyst development in the kidneys of inv mutant mice,” Kidney International, vol. 79, no. 9, pp. 957–965, 2011.
- L. Eley, L. Turnpenny, L. M. Yates et al., “A perspective on inversin,” Cell Biology International, vol. 28, no. 2, pp. 119–124, 2004.
- C. Bergmann, M. Fliegauf, N. O. Brüchle et al., “Loss of nephrocystin-3 function can cause embryonic lethality,meckel-gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia,” American Journal of Human Genetics, vol. 82, no. 4, pp. 959–970, 2008.
- V. H. Gattone II, X. Wang, P. C. Harris, and V. E. Torres, “Inhibition of renal cystic disease development and progression by a vasopressin V2 receptor antagonist,” Nature Medicine, vol. 9, no. 10, pp. 1323–1326, 2003.
- J. Hoefele, R. Sudbrak, R. Reinhardt et al., “Mutational analysis of the NPHP4 gene in 250 patients with nephronophthisis,” Human Mutation, vol. 25, no. 4, p. 411, 2005.
- H. H. Arts, D. Doherty, S. E. C. Van Beersum et al., “Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome,” Nature Genetics, vol. 39, no. 7, pp. 882–888, 2007.
- M. Delous, L. Baala, R. Salomon et al., “The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome,” Nature Genetics, vol. 39, no. 7, pp. 875–881, 2007.
- M. Delous, N. E. Hellman, H. M. Gaudé et al., “Nephrocystin-1 and nephrocystin-4 are required for epithelial morphogenesis and associate with PALS1/PATJ and Par6,” Human Molecular Genetics, vol. 18, no. 24, pp. 4711–4723, 2009.
- T. Schäfer, M. Pütz, S. Lienkamp et al., “Genetic and physical interaction between the NPHP5 and NPHP6 gene products,” Human Molecular Genetics, vol. 17, no. 23, pp. 3655–3662, 2008.
- A. I. Den Hollander, R. K. Koenekoop, S. Yzer et al., “Mutations in the CEP290 (NPHP6) gene are a frequent cause of leber congenital amaurosis,” American Journal of Human Genetics, vol. 79, no. 3, pp. 556–561, 2006.
- C. C. Leitch, N. A. Zaghloul, E. E. Davis et al., “Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome,” Nature Genetics, vol. 40, no. 4, pp. 443–448, 2008.
- N. T. Gorden, H. H. Arts, M. A. Parisi et al., “CC2D2A is mutated in joubert syndrome and interacts with the ciliopathy-associated Basal Body Protein CEP290,” American Journal of Human Genetics, vol. 83, no. 5, pp. 559–571, 2008.
- S. Mougou-Zerelli, S. Thomas, E. Szenker et al., “CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation,” Human Mutation, vol. 30, no. 11, pp. 1574–1582, 2009.
- D. Huangfu, A. Liu, A. S. Rakeman, N. S. Murcia, L. Niswander, and K. V. Anderson, “Hedgehog signalling in the mouse requires intraflagellar transport proteins,” Nature, vol. 426, no. 6962, pp. 83–87, 2003.
- H. Khanna, E. E. Davis, C. A. Murga-Zamalloa et al., “A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies,” Nature Genetics, vol. 41, no. 6, pp. 739–745, 2009.
- E. Sohara, Y. Luo, J. Zhang, D. K. Manning, D. R. Beier, and J. Zhou, “Nek8 regulates the expression and localization of polycystin-1 and polycystin-2,” Journal of the American Society of Nephrology, vol. 19, no. 3, pp. 469–476, 2008.
- K. L. M. Coene, R. Roepman, D. Doherty et al., “OFD1 is mutated in X-linked joubert syndrome and interacts with LCA5-encoded lebercilin,” American Journal of Human Genetics, vol. 85, no. 4, pp. 465–481, 2009.
- D. Doherty, M. A. Parisi, L. S. Finn et al., “Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis),” Journal of Medical Genetics, vol. 47, no. 1, pp. 8–21, 2010.
- L. Baala, S. Audollent, J. Martinovic et al., “Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel syndrome,” American Journal of Human Genetics, vol. 81, no. 1, pp. 170–179, 2007.
- H. R. Dawe, U. M. Smith, A. R. Cullinane et al., “The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation,” Human Molecular Genetics, vol. 16, no. 2, pp. 173–186, 2007.
- H. R. Dawe, M. Adams, G. Wheway et al., “Nesprin-2 interacts with meckelin and mediates ciliogenesis via remodelling of the actin cytoskeleton,” Journal of Cell Science, vol. 122, no. 15, pp. 2716–2726, 2009.
- E. M. Valente, C. V. Logan, S. Mougou-Zerelli et al., “Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes,” Nature Genetics, vol. 42, no. 7, pp. 619–625, 2010.
- S. J. Ansley, J. L. Badano, O. E. Blacque et al., “Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome,” Nature, vol. 425, no. 6958, pp. 628–633, 2003.
- N. F. Berbari, A. K. O'Connor, C. J. Haycraft, and B. K. Yoder, “The primary cilium as a complex signaling center,” Current Biology, vol. 19, no. 13, pp. R526–R535, 2009.
- S. M. Nauli, F. J. Alenghat, Y. Luo et al., “Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells,” Nature Genetics, vol. 33, no. 2, pp. 129–137, 2003.
- X. Wang, Y. Wu, C. J. Ward, P. C. Harris, and V. E. Torres, “Vasopressin directly regulates cyst growth in polycystic kidney disease,” Journal of the American Society of Nephrology, vol. 19, no. 1, pp. 102–108, 2008.
- M. K. Raychowdhury, A. J. Ramos, P. Zhang et al., “Vasopressin receptor-mediated functional signaling pathway in primary cilia of renal epithelial cells,” American Journal of Physiology, vol. 296, no. 1, pp. F87–F97, 2009.
- V. Marion, D. Schlicht, A. Mockel, et al., “Bardet-Biedl syndrome highlights the major role of the primary cilium in efficient water reabsorption,” Kidney International, vol. 79, no. 9, pp. 1013–1025, 2011.
- G. G. Germino, “Linking cilia to Wnts,” Nature Genetics, vol. 37, no. 5, pp. 455–457, 2005.
- G. J. Pazour, B. L. Dickert, Y. Vucica et al., “Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene Tg737, are required for assembly of cilia and flagella,” Journal of Cell Biology, vol. 151, no. 3, pp. 709–718, 2000.
- M. A. Lancaster and J. G. Gleeson, “Cystic kidney disease: the role of Wnt signaling,” Trends in Molecular Medicine, vol. 16, no. 8, pp. 349–360, 2010.
- S. Saadi-Kheddouci, D. Berrebi, B. Romagnolo et al., “Early development of polycystic kidney disease in transgenic mice expressing an activated mutant of the β-catenin gene,” Oncogene, vol. 20, no. 42, pp. 5972–5981, 2001.
- M. A. Lancaster, C. M. Louie, J. L. Silhavy et al., “Impaired Wnt-β-catenin signaling disrupts adult renal homeostasis and leads to cystic kidney ciliopathy,” Nature Medicine, vol. 15, no. 9, pp. 1046–1054, 2009.
- E. Fischer and M. Pontoglio, “Planar cell polarity and polycystic kidney disease,” Médecine Sciences, vol. 22, no. 6-7, pp. 576–578, 2006.
- E. Fischer, E. Legue, A. Doyen et al., “Defective planar cell polarity in polycystic kidney disease,” Nature Genetics, vol. 38, no. 1, pp. 21–23, 2006.
- M. Simons and G. Walz, “Polycystic kidney disease: cell division without a c(l)ue?” Kidney International, vol. 70, no. 5, pp. 854–864, 2006.
- S. Saburi, I. Hester, E. Fischer et al., “Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease,” Nature Genetics, vol. 40, no. 8, pp. 1010–1015, 2008.
- J. M. Shillingford, N. S. Murcia, C. H. Larson et al., “The mTOR pathway is regulated by polycystin-1, and its inhibition reverses renal cystogenesis in polycystic kidney disease,” Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no. 14, pp. 5466–5471, 2006.
- S. J. Leuenroth, N. Bencivenga, P. Igarashi, S. Somlo, and C. M. Crews, “Triptolide reduces cystogenesis in a model of ADPKD,” Journal of the American Society of Nephrology, vol. 19, no. 9, pp. 1659–1662, 2008.
- N. O. Bukanov, L. A. Smith, K. W. Klinger, S. R. Ledbetter, and O. Ibraghimov-Beskrovnaya, “Long-lasting arrest of murine polycystic kidney disease with CDK inhibitor roscovitine,” Nature, vol. 444, no. 7121, pp. 949–952, 2006.
- L. I. Zon and R. T. Peterson, “In vivo drug discovery in the zebrafish,” Nature Reviews Drug Discovery, vol. 4, no. 1, pp. 35–44, 2005.