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Experimental Diabetes Research
Volume 2008 (2008), Article ID 697035, 8 pages
Human Islet Amyloid Polypeptide Transgenic Mice: In Vivo and Ex Vivo Models for the Role of hIAPP in Type 2 Diabetes Mellitus
1Division of Biomedical Genetics, Department of Metabolic and Endocrine Diseases, University Medical Center Utrecht, P.O. Box 85090, 3508 AB Utrecht, The Netherlands
2Netherlands Metabolomics Centre, location Utrecht, P.O. Box 85090, 3508 AB Utrecht, The Netherlands
3Division Laboratories and Pharmacy, Department of Endocrinology, University Medical Center Utrecht, P.O. Box 85090, 3508 AB Utrecht, The Netherlands
4Department of Experimental Medical Sciences, Lund University, BMC, C 12, S-221 84 Lund, Sweden
5Division of Medical Biology, Department of Pathology and Laboratory Medicine, University of Groningen, Hanzeplein 1, 9700 RB, Groningen, The Netherlands
6Department of Clinical Sciences, Lund University, BMC, C 12, S-221 84 Lund, Sweden
Received 9 October 2007; Revised 30 January 2008; Accepted 14 February 2008
Academic Editor: Hiroshi Okamoto
Copyright © 2008 J. W. M. Höppener 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.
Human islet amyloid polypeptide (hIAPP), a pancreatic islet protein of 37 amino acids, is the main component of islet amyloid, seen at autopsy in patients with type 2 diabetes mellitus (DM2). To investigate the roles of hIAPP and islet amyloid in DM2, we generated transgenic mice expressing hIAPP in their islet beta cells. In this study, we found that after a long-term, high-fat diet challenge islet amyloid was observed in only 4 of 19 hIAPP transgenic mice. hIAPP transgenic females exhibited severe glucose intolerance, which was associated with a downregulation of GLUT-2 mRNA expression. In isolated islets from hIAPP males cultured for 3 weeks on high-glucose medium, the percentage of amyloid containing islets increased from 5.5% to 70%. This ex vivo system will allow a more rapid, convenient, and specific study of factors influencing islet amyloidosis as well as of therapeutic strategies to interfere with this pathological process.
Islet amyloid polypeptide (IAPP), also referred to as amylin, is a 37 amino acid protein produced in the pancreatic islet beta cells. Human IAPP (hIAPP) is implicated in the pathophysiology of type 2 diabetes mellitus (DM2) since it forms proteinaceous tissue deposits in the pancreatic islets (“islet amyloid”) [1–3]. Islet amyloid has been demonstrated in more than 80% of patients with DM2 [4, 5]. Islet amyloid formation is implicated in development of beta cell failure which, in addition to insulin resistance, is a characteristic of DM2 . Overproduction of IAPP in insulin resistance may occur due to common transcription regulatory elements in the promoter regions of the IAPP and insulin genes , and this might underly the enhanced amyloid formation in DM2 . This in turn may induce impairment of beta cell function since aggregation of hIAPP has been demonstrated to be cytotoxic [8–10]. However, involvement of islet amyloid in development of DM2 is still not firmly established. Recent data, both for hIAPP and for other amyloidogenic proteins (notably the Alzheimer’s disease-related Abeta peptide), indicate that the degree of amyloid formation does not correspond with the severity of disease [11, 12]. In addition, prefibrillar aggregates of amyloidogenic proteins seem to be more cytotoxic than mature amyloid fibrils [13, 14]. To explore the potential diabetogenic effects of hIAPP and islet amyloid, we have generated transgenic mice overproducing biologically active hIAPP in the islet beta cells [15–17] (mouse IAPP does not form islet amyloid). We previously showed that hIAPP overexpression in itself does not induce hyperglycemia, hyperinsulinemia, or obesity in these mice . However, when the hIAPP transgenic mice were crossbred with leptin-deficient and insulin-resistant ob/ob mice, extensive islet amyloid formation with worsening of the diabetes was observed . In the present paper, we describe two experimental studies. In an in vivo experiment, we examined the influence of transgenic hIAPP expression on glucose tolerance of mice on a high-fat diet for a long period of time. Previous studies had shown that long-term, high-fat diet induces hyperglycemia, hyperinsulinemia, and obesity in mice [19, 20]. Furthermore, high-fat diet may be involved in islet amyloid formation in hIAPP transgenic mice . We, thus, administered a high-fat diet for 14 months to hIAPP transgenic and nontransgenic (control) mice and report here the islet amyloid formation, glucose tolerance, and islet GLUT-2 mRNA expression. In addition, we describe the development of an ex vivo model system for islet amyloidosis, using pancreatic islets isolated from the hIAPP transgenic mice. When such islets were cultured in high-glucose medium, amyloid formation occurs more rapidly as compared to the in vivo situation. Thus, this ex vivo model system will enable to study the process and effects of islet amyloid formation more specifically and conveniently.
2. Materials and Methods
The generation of C57Bl/6J hIAPP transgenic mice with a rat insulin-2 gene promoter fragment (position −695 to +8 relative to the transcription start site) linked to the hIAPP gene has previously been described . The hIAPP transgenic mice were maintained by breeding heterozygous transgenic mice with mates of the C57BL/6J strain. Transgenic mice were differentiated from nontransgenic (NT) littermates by dot blot Southern hybridization, using a 588 bp hIAPP-specific DNA probe . Mice were housed on hardwood bedding in polypropylene cages and maintained in air-conditioned rooms at 20–22°C with a photoperiod of 12 hours light, 12 hours dark. Water was available continuously and the mice received ad libitum a regular diet until 2.5 months of age. This diet contained 4,500 kcal/kg and included 22.5% protein and 4.8% fat (Hope Farms, Woerden, The Netherlands). At 2.5 months of age, the diet was switched to a high-fat diet for 14 months containing 5,600 kcal/kg, 20.8% protein, and 36.0% fat (30.0% cocoa oil, 6.0% corn oil; Hope Farms).
2.2. Glucose Tolerance Test
At 14 months after the start of the high-fat diet, nonfasted mice were anaesthetized with an i.p. injection of midazolam (0.4 mg/mouse) (Dormicum, Hoffman-La-Roche, Basel, Switzerland), and a combination of fluanison (0.9 mg/mouse), and fentanyl (0.02 mg/mouse) (Hypnorm, Janssen, Beerse, Belgium). D-glucose (British Drug Houses, Poole, UK) was injected i.p. (1 g/kg) and blood was sampled from the retrobulbar, intraorbital, capillary plexus before glucose administration and after 10, 30, 60, and 120 minutes. The samples were taken in heparinized tubes and stored on ice. Following centrifugation, plasma was separated and stored at −20°C until analysis. After the 120-minute blood sample, tissue was sampled (see below), and trunk blood was obtained for measurement of IAPP levels. The blood was collected in EDTA-tubes and kept on ice until centrifugation at 1500 g for 5 minutes at 4°C. Plasma was stored at −80°C.
All animal experiments were approved by the Animal Welfare Committee of Utrecht University/University Medical Center Utrecht, The Netherlands.
2.3. Plasma Measurements
IAPP levels were measured in 25–100 ul plasma by RIA as described , using a rabbit, polyclonal hIAPP antiserum (K1338) that shows full cross-reactivity with synthetic amidated rat/mouse IAPP . Free and bound radioactivity was separated by use of double antibody immunoprecipitation. The sensitivity of the assay is 3.5 pmol/l and the coefficiency of variation <10% at both low and high levels. Insulin levels were measured in 20 ul plasma by RIA using guinea pig anti-rat insulin antibody, 125I-labelled human insulin as tracer and rat insulin as standard (Linco Research, St. Charles, Mo, USA). Free and bound radioactivity was separated by use of an anti-IgG antibody (Linco). The sensitivity of the assay is 12 pmol/l and the coefficiency of variation <3% at both low and high levels. Glucose was determined in 10 ul plasma by the glucose oxidase method.
2.4. Histological Analysis of Pancreatic Tissue
Pancreatic tissue samples were fixed in 3.7% phosphate-buffered formalin (pH 7.4) for 24–48 hours and paraffin embedded. Sections of 5 μm were stained with Congo red for detection of islet amyloid by polarized light microscopy (“apple-green” birefringence) and fluorescence light microscopy (red-coloured autofluorescence). At least 10 islets per mouse were examined. The percentage of individual islet areas occupied by amyloid, as indicated by Congo red positive staining, was visually estimated and scored as follows: 0% = score 0, between 0 and 26% = score 1, 26–50% = score 2, 51–75% = score 3, and 76–100% = score 4. The Amyloid Index (range: 0–100) of an individual mouse was calculated as , where is the number of islets with score 1, the number with score 2, and so on, and n is the total number of islets investigated. The degree of islet amyloid formation was determined with the investigator being unaware of the genetic status of the animals (i.e., “blind”).
To examine the cellular expression of GLUT-2 mRNA, paraffin sections were subjected to in situ hybridization using a previously described protocol  and a 35S-labelled oligonucleotide probe covering the nucleotide sequence 247–276 of mouse GLUT-2 cDNA . In order to confirm beta cell expression of hIAPP mRNA in the transgenic mice, sections were also hybridized with a 35S-labelled oligonucleotide probe specific for hIAPP mRNA .
2.5. Image Analysis and Morphometry
In situ hybridization radiolabelling was examined in a bright field microscope (Olympus, BX60), and images were captured with a digital camera (Olympus, DP50). To quantify the density of labelling for GLUT-2 mRNA within islets, areas of in situ hybridization radiolabelling were calculated. Islets (5–8 per animal) were randomly selected from different parts of the sections from 4 mice, 2 males and 2 females in each group. The transgenic mice analyzed were rated as negative for amyloid. The labelled area, that is, grain density within an islet, and total islet area were measured, using NIH-image software, and the density of labelling was expressed as percentage of the total islet area [23, 26]. All sections used were hybridized simultaneously and under identical conditions.
2.6. Isolation of Pancreatic Islets
For islet isolation, transgenic mice were bred to homozygosity for the hIAPP transgenic locus. Homozygotes were discriminated from heterozygous and nontransgenic littermates by dot blot Southern hybridization of tail DNA using a human-specific IAPP probe  and quantification of the hybridization signal using phosphor imaging and Image-Quant software (Molecular Dynamics, Inc. Krefeld, Germany).
Islets were isolated from the pancreas of 6-month-old hIAPP transgenic male mice, essentially as previously described . Briefly, under halothane anaesthesia, the abdomen was opened. The pancreas was excised starting from the spleen site to the duodenum. Subsequently, the pancreas was brougth in 10 mL sterile Krebs-Ringer-buffer supplemented with 25 mmol/L Hepes (KRH) and containing 10% Bovine Serum Albumin (BSA) at 4°C. Next, the pancreas was chopped, digested using a two-stage incubation of 20 minutes at 37°C with successively 1.0 and 0.7 mg/mL collagenase (Sigma type XI, Sigma, St Louis, MO, USA). Islets were separated from exocrine tissue by centrifugation over a discontinuous dextran gradient  and further purified by handpicking into 9 cm petridishes with 12 mL KRH buffer, pH = 7.4, supplemented with 10% BSA penicillin (100 units/mL)/streptomycin (0.1 mg/mL) (KRH 10% BSA P/S) and glucose to a concentration of 11 mM. Two days after isolation, the islets from 12 mice were pooled, mixed and split into portions. Four portions of 75 islets each were fixed and embedded for amyloid quantification. Eight portions of approximately 90 islets were transferred to culture medium with 28 mM glucose. Medium was changed every 2-3 days, switching between 11 mM and 28 mM of glucose (to prevent possible desensitization of the beta cells). Islets were counted, while being picked into the dishes with fresh medium. At 3 weeks after islet isolation, the cultured islets were fixed and embedded for amyloid quantification.
2.7. Fixation and Embedding of Pancreatic Islets
Islets were washed with phosphate buffered saline (PBS), and fixed in 0.5 mL islets fixative (2% paraformaldehyde, 0.2% glutaraldehyde in 0.1 M Sörensen buffer) for 2 hours at room temperature. Fixative was removed and islets were washed with 0.5 mL 0.1 M Sörensen buffer. Sörensen buffer was removed and islets were resuspended in 30 l 37°C heated 12% gelatin, cooled on ice and stored at −20°C.
2.8. Amyloid Quantification in Cultured Islets
From the gelatin-embedded islet blocks, 5 m frozen sections were cut onto Superfrost Plus microscope slides (Menzel-Gläser) and stored at −20°C until further use. Sections were fixed in acetone for 1′, rehydrated in PBS for 15′, stained with heamatoxylin for 1′, washed in running tap water for 5′, and stained with Congo red (1 g/liter saturated sodium chloride 80% ethanol, into which 10 mL/liter 1% sodium hydroxide was added just before staining) for 30′. After dehydration in an augmenting ethanol series (70%, 96%, 100%) and xylene (twice), sections were enclosed with Depex. Amyloid-containing paraffin sections of hIAPP transgenic mouse pancreatic tissue were used as positive control for the Congo red staining.
For the detection of amyloid, Congo red-stained islet sections were examined using a fluorescence microscope. Amyloid deposits were visible as bright red autofluorescent areas without cells, which showed a green birefringence upon visualization with polarized light. An islet was scored as amyloid positive if at least 2 successive sections of that islet contained Congo red-positive amyloid deposits. The scoring was performed in a “blind” fashion, that is, with the investigator unaware of the source of the islets.
2.9. Statistical Analysis
Values are means ±SEM, unless stated otherwise. P-values indicate the probability level of random difference between groups, or of random correlation, respectively. P-values <.05 were considered to represent statistical significance. Nonparametric T-tests were used to compare 2 independent samples (Mann-Whitney-U test: hIAPP versus NT, male versus female). Data of the mRNA in situ hybridizations were analyzed by Student’s unpaired t-test. Differences in percentage of amyloid-positive islets between 2 days and 3 weeks of culture were analyzed by use of one-way analysis of variance (ANOVA). Probability values of less than .01 were considered significant.
3.1. Body Weight and Plasma IAPP Levels
Body weight after 14 months on the high-fat diet did not differ between the groups, being 57 ± 0.8 g versus 58 ± 0.9 g in male hIAPP () and NT () mice, and 59 ± 1.1 g versus 64 ± 3 g in female hIAPP () and NT () mice. Plasma IAPP levels were 462 ± 78 pmol/L in male hIAPP mice versus 195 ± 32 pmol/L in male NT mice, and 346 ± 81 pmol/L in female hIAPP mice versus 130 ± 21 pmol/L in female NT mice, being significantly higher in hIAPP mice of both genders (P < .01) without any gender difference.
3.2. Glucose Tolerance Test
After 14 months on the high-fat diet, nonfasted plasma glucose and insulin levels were not different between hIAPP and NT mice of the same gender. However, both for the hIAPP and NT mice, plasma insulin levels were higher in males as compared to females (Figure 1). When glucose was administered i.p. (1 g/kg), the insulin response to glucose and the glucose elimination were similar in hIAPP and NT male mice. In contrast, in female hIAPP mice, plasma glucose levels after the i.p. glucose challenge were markedly higher at all time points as compared to female NT mice (P < .05 or P < .01) in association with increased insulin levels 30 minutes after glucose administration (P < .01). Hence, hIAPP overproduction was associated with severe impairment of glucose elimination in female but not in male mice after high-fat diet.
3.3. Pancreatic Islet Amyloid Formation
Islet amyloid was detected in 4/19 hIAPP mice on high-fat diet but in none of the 11 NT mice. The Amyloid Index for these 4 mice was (average and SD). There was no gender difference in islet amyloid formation in hIAPP transgenic mice (3/8 in males versus 1/11 in females).
3.4. Islet GLUT-2 mRNA Expression
As expected, a strong hIAPP mRNA labeling was observed in the islets of all transgenic mice, while it was lacking in all NT mice (Figures 2(a), 2(b)). GLUT-2 mRNA labeling of weak to moderate density was observed in the islets of NT mice (Figure 2(c)), with no overt difference between female and male mice. In the transgenic mice, however, the GLUT-2 mRNA labeling was generally weaker, and even barely detectable in some female mice (Figure 2(d)). The GLUT-2 mRNA signal was reduced in all transgenic mice, regardless of the presence or absence of islet amyloid. Image analysis revealed a significant reduction of GLUT-2 mRNA labeling of islets in hIAPP transgenic versus NT mice (P = .02, Figure 3).
3.5. Ex Vivo Survival and Amyloid Formation in Cultured hIAPP Transgenic Pancreatic Islets
The percentage of 3-week survival of hIAPP transgenic islets was 83.8 ± 1.0% (). Of all islet cultures, 22–30 islets were scored for the presence of amyloid. The percentage of amyloid-positive islets significantly increased (P < .001) from % () after 2 days of culture to 70 ± 3.1% () at the end of the culture period. Thus, the percentage of amyloid-positive islets increased more than 10 times in three weeks of culture at high glucose conditions in this ex vivo islet amyloidosis system. An example of a cultured hIAPP transgenic islet containing amyloid is shown in Figure 4.
4.1. High-Fat Diet and Amyloid Formation
In this study, transgenic mice overproducing the amyloidogenic hIAPP in their pancreatic islet beta cells, as well as NT control mice, were fed a high-fat diet for 14 months, in order to evaluate the impact on islet amyloid formation and glucose homeostasis when combining these two potentially diabetogenic factors. We anticipated a marked islet amyloid formation in the hIAPP transgenic mice on the high-fat diet because we previously observed that crossbreeding the hIAPP transgenic mice with the Obese mouse (being severly insulin resistant) resulted in extensive islet amyloid formation . Also, when insulin resistance was induced in hIAPP mice by crossbreeding with the obese Agouti viable yellow mice  or by exogenous growth hormone and glucocorticoids , islet amyloid formation was promoted. In addition, high-fat feeding induced islet amyloid formation in approximately 80% of male mice in another hIAPP transgenic colony . However, we found that only four out of the 19 hIAPP mice (approx. 40% of the males) that were followed for 14 months on the high-fat diet did develop islet amyloid. This lower frequency might be due to differences in the genetic background and/or the composition of the diet, influencing insulin resistance and IAPP expression. The amyloid index in those four high-fat fed mice was higher than in six of 33 similarly aged hIAPP mice (approx. 30% of the males) which developed amyloid on a regular diet ( versus , ) . This indicates that although long-term, high-fat diet indeed has the capacity to promote islet amyloid formation in these hIAPP transgenic mice, the efficiency is not high. Crossbreeding the hIAPP mice with leptin-deficient Obese mice introduced more severe obesity and insulin resistance  as compared to the high-fat diet. Consequently, these other factors seem of importance for the promotion of islet amyloid formation. Another factor might be hyperglycemia, which is more severe in the hIAPP ob/ob mice as compared to the hIAPP mice on high-fat diet. Such a hypothesis is supported by the finding that in isolated pancreatic islets of our hIAPP mice, islet amyloid was detected by electron microscopy after culture in high-glucose medium but not in low-glucose medium . Other mechanisms may, however, also be of importance.
4.2. High Fat Diet and Glucose Tolerance
In this study, we also observed severe glucose intolerance in female but not in male hIAPP transgenic mice. The finding that in all groups of mice plasma insulin levels failed to return to basal within 2 hours after the glucose load is in accordance with high-fat diet inducing insulin resistance . Also, the higher insulin levels in male mice versus female mice is well known from previous studies . Thus, our data indicate that the overproduction of insulin in response to insulin resistance after high-fat diet was adequate in hIAPP males but not in hIAPP females. Since there was no gender difference in the amyloid formation in high-fat fed hIAPP mice, these results suggest that a metabolic impact of high levels of circulating IAPP underlies the gender difference in glucose tolerance of hIAPP transgenic mice after high-fat diet. IAPP has, thus, been shown to inhibit insulin secretion [34, 35] as well as to inhibit glycogen synthesis in rat muscle tissue  through inhibition of glycogen synthase and stimulation of glycogen phosphorylase . In addition, it has been observed that IAPP administration induces insulin resistance in rats , although no such effect was evident in humans . IAPP has also in some studies  but not in others  been shown to increase liver glucose production. Whether these actions show gender differences, and thus may explain the remarkable glucose intolerance observed in female but not in male hIAPP transgenic mice on the high-fat diet, is not known. Indeed, it is striking that although male rodents generally are more prone to insulin resistance than females, the hIAPP transgenic females on high-fat diet are more glucose intolerant than their male littermates. Since insulin levels are not lower in the hIAPP females compared to the NT females, these data suggest that insulin sensitivity is impaired in the female hIAPP mice.
4.3. High-Fat Diet and GLUT-2 Expression
Islet GLUT-2 mRNA expression was reduced in hIAPP transgenic versus NT mice, and this reduction appeared more severe in female than in male mice. Beta cell GLUT-2 expression is known to correlate with glucose responsiveness of the cells . However, insulin levels were not reduced in the male or female hIAPP mice. Therefore, it is presently not known if and how the reduced GLUT-2 mRNA expression among the transgenic mice might be related to the glucose intolerance in the female hIAPP mice. Also, the mechanism of hIAPP mediated downregulation of islet GLUT-2 mRNA expression is unknown, but our data indicate that in addition to inhibition of insulin action in muscle [33, 34] IAPP can (in) directly inhibit glucose responsiveness of islet beta cells by affecting GLUT-2 expression.
In conclusion, this in vivo study shows that promoting insulin resistance over a long period of time by giving a high-fat diet for 14 months promotes islet amyloid formation in hIAPP transgenic mice, although less extensively than in the severe insulin-resistant Obese, leptin-deficient hIAPP mice. This suggests that the degree of insulin resistance is important for extensive development of islet amyloid. In addition, we observed a remarkable gender difference in that severe glucose intolerance was observed only in female hIAPP transgenic mice given high-fat diet and not in males. We suggest that this gender difference is due to the high level of circulating IAPP rather than to islet amyloid formation. If and how this glucose intolerance might be mediated by downregulation of beta cell GLUT-2 gene expression, as observed in the hIAPP mice, is presently unknown.
4.4. Ex Vivo Islet Amyloidosis Model
The rationale for the ex vivo study was to examine if amyloid would be formed in isolated and cultured pancreatic islets from hIAPP mice, to such a degree that it would be detectable with light microscopy. Since both the present and previous  in vivo data indicated the development of islet amyloid notably in male hIAPP mice, we decided to investigate amyloid formation in such islets specifically from male mice. To increase the potential for amyloid formation, we bred the mice to homozygosity for the hIAPP transgene. At an age of 6 months, homozygous transgenic hIAPP males had islet amyloid in about 5% of their pancreatic islets, at 2 days after islet isolation. Previously, we detected amyloid fibrils by electron microscopy in islets from 4–10 months old heterozygous hIAPP transgenic mice, cultured for 1 week in medium with 11 or 28 mM glucose . With the present model, using islets from 6-month-old homozygous hIAPP transgenic males, cultured in medium with high glucose (switching between 11 and 28 mM), we can detect amyloid deposits with Congo red staining and light microscopy, thus enabling quantification of the degree of islet amyloidosis. The number of amyloid-positive islets increased more than 10 fold (from 5.5 to 70%) after 3 weeks of culture in medium containing a high glucose concentration. Although an accurate comparison between the degrees of islet amyloid formation in vivo and ex vivo was not made, our data certainly indicate stronger islet amyloid formation in hIAPP islets cultured ex vivo as compared to in vivo. This might be explained by the higher glucose concentrations in the ex vivo system. hIAPP transgenic mice in vivo have normal plasma glucose concentrations [15, 18], whereas ex vivo the glucose concentration in the medium switched between 11 and 28 mM. It is known that a high glucose concentration triggers both insulin and IAPP secretion, and the hIAPP transgene is under control of an insulin promoter. In addition, macrophages have been implicated in in vivo removal of (beginning) amyloid deposits  and such macrophages are absent in the ex vivo system, potentially allowing increased amyloid formation. When combined with a more accurate amyloid quantification procedure involving image analysis, this ex vivo system may present a fast and convenient model to study the process (and factors involved) of islet amyloidosis, as well as the detrimental consequences for individual beta cells (apoptosis) and islet function (insulin producing capacity). In addition, such a model system might be used as an amyloidosis assay to assess the potency of known and novel therapeutic strategies, aimed at reducing, or even preventing, islet amyloid formation, and its effects on beta cell and islet function.
The authors wish to thank Lena Kvist (Lund University, Lund), Bart de Haan (University of Groningen), Gerard Graad (Department of Endocrinology, UMC Utrecht), Renske Luneborg-Van Netten (Department of Pathology, UMC Utrecht), Herma Boere and Toon Hesp (Animal House Utrecht University) for expert technical assistance and Dr. P. Westers (Center for Biostatistics, Utrecht University) for advice on statistical analyses. This study was supported by grants from the Dutch Diabetes Fund (Grant DFN 92.133) as well as from the Swedish Medical Research Council (Grants no. 14X-6834 and 72X-4499), Albert Påhlsson, Novo Nordic and Crafoord Foundations, Swedish Diabetes Association.
- P. Westermark, C. Wernstedt, E. Wilander, D. W. Hayden, T. D. O'Brien, and K. H. Johnson, “Amyloid fibrils in human insulinoma and islets of Langerhans of the diabetic cat are derived from a neuropeptide-like protein also present in normal islet cells,” Proceedings of the National Academy of Sciences of the United States of America, vol. 84, no. 11, 3881 pages, 1987.
- S. E. Kahn, S. Andrikopoulos, and C. B. Verchere, “Islet amyloid: a long-recognized but underappreciated pathological feature of type 2 diabetes,” Diabetes, vol. 48, no. 2, 241 pages, 1999.
- J. W. M. Höppener, B. Ahrén, and C. J. M. Lips, “Islet amyloid and type 2 diabetes mellitus,” The New England Journal of Medicine, vol. 343, no. 6, 411 pages, 2000.
- P. Westermark, “Fine structure of islets of Langerhans in insular amyloidosis,” Virchows Archiv, vol. 359, no. 1, 1 pages, 1973.
- A. Clark, C. A. Wells, I. D. Buley, et al., “Islet amyloid, increased A-cells, reduced B-cells and exocrine fibrosis: quantitative changes in the pancreas in type 2 diabetes,” Diabetes Research, vol. 9, no. 4, 151 pages, 1988.
- C. J. Rhodes, “Type 2 diabetes-a matter of -cell life and death?” Science, vol. 307, no. 5708, 380 pages, 2005.
- M. German, L. G. Moss, J. Wang, and W. J. Rutter, “The insulin and islet amyloid polypeptide genes contain similar cell-specific promoter elements that bind identical B-cell nuclear complexes,” Molecular Cell Biology, vol. 12, no. 4, 1777 pages, 1992.
- A. Lorenzo, B. Razzaboni, G. C. Weir, and B. A. Yankner, “Pancreatic islet cell toxicity of amylin associated with type-2 diabetes mellitus,” Nature, vol. 368, no. 6473, 756 pages, 1994.
- J. Janson, R. H. Ashley, D. Harrison, S. McIntyre, and P. C. Butler, “The mechanism of islet amyloid polypeptide toxicity is membrane disruption by intermediate-sized toxic amyloid particles,” Diabetes, vol. 48, no. 3, 491 pages, 1999.
- J. W. M. Höppener and C. J. M. Lips, “Role of islet amyloid in type 2 diabetes mellitus,” International Journal of Biochemistry and Cell Biology, vol. 38, no. 5-6, 726 pages, 2006.
- J. S. Jacobsen, C.-C. Wu, J. M. Redwine, et al., “Early-onset behavioral and synaptic deficits in a mouse model of Alzheimer's disease,” Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no. 13, 5161 pages, 2006.
- A. E. Butler, J. Janson, W. C. Soeller, and P. C. Butler, “Increased -cell apoptosis prevents adaptive increase in -cell mass in mouse model of type 2 diabetes: evidence for role of islet amyloid formation rather than direct action of amyloid,” Diabetes, vol. 52, no. 9, 2304 pages, 2003.
- M. Bucciantini, G. Calloni, F. Chiti, et al., “Prefibrillar amyloid protein aggregates share common features of cytotoxicity,” Journal of Biological Chemistry, vol. 279, no. 30, 31374 pages, 2004.
- R. Kayed, E. Head, J. L. Thompson, et al., “Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis,” Science, vol. 300, no. 5618, 486 pages, 2003.
- J. W. M. Höppener, J. S. Verbeek, E. J. P. de Koning, et al., “Chronic overproduction of islet amyloid polypeptide/amylin in transgenic mice: lysosomal localization of human islet amyloid polypeptide and lack of marked hyperglycaemia or hyperinsulinaemia,” Diabetologia, vol. 36, no. 12, 1258 pages, 1993.
- K. L. van Hulst, W. Born, R. Muff, et al., “Biologically active human islet amyloid polypeptide/amylin in transgenic mice,” European Journal of Endocrinology, vol. 136, no. 1, 107 pages, 1997.
- B. Ahrén, C. Oosterwijk, C. J. M. Lips, and J. W. M. Höppener, “Transgenic overexpression of human islet amyloid polypeptide inhibits insulin secretion and glucose elimination after gastric glucose gavage in mice,” Diabetologia, vol. 41, no. 11, 1374 pages, 1998.
- J. W. M. Höppener, C. Oosterwijk, M. G. Nieuwenhuis, et al., “Extensive islet amyloid formation is induced by development of type II diabetes mellitus and contributes to its progression: pathogenesis of diabetes in a mouse model,” Diabetologia, vol. 42, no. 4, 427 pages, 1999.
- R. S. Surwit, C. M. Kuhn, C. Cochrane, J. A. McCubbin, and M. N. Feinglos, “Diet-induced type II diabetes in C57BL/6J mice,” Diabetes, vol. 37, no. 9, 1163 pages, 1988.
- B. Ahrén, E. Simonsson, A. J. W. Scheurink, H. Mulder, U. Myrsén, and F. Sundler, “Dissociated insulinotropic sensitivity to glucose and carbachol in high-fat diet-induced insulin resistance in C57 BL/6J mice,” Metabolism, vol. 46, no. 1, 97 pages, 1997.
- C. B. Verchere, D. A. D'Alessio, R. D. Palmiter, et al., “Islet amyloid formation associated with hyperglycemia in transgenic mice with pancreatic -cell expression of human islet amyloid polypeptide,” Proceedings of the National Academy of Sciences of the United States of America, vol. 93, no. 8, 3492 pages, 1996.
- K. L. van Hulst, W. H. L. Hackeng, J. W. M. Höppener, et al., “An improved method for the determination of islet amyloid polypeptide levels in plasma,” Annals of Clinical Biochemistry, vol. 31, no. 2, 165 pages, 1994.
- H. Mulder, B. Ahrén, M. Stridsberg, and F. Sundler, “Non-parallelism of islet amyloid polypeptide (amylin) and insulin gene expression in rat islets following dexamethasone treatment,” Diabetologia, vol. 38, no. 4, 395 pages, 1995.
- B. Thorens, H. K. Sarkar, H. R. Kaback, and H. F. Lodish, “Cloning and functional expression in bacteria of a novel glucose transporter present in liver, intestine, kidney, and -pancreatic islet cells,” Cell, vol. 55, no. 2, 281 pages, 1988.
- H. Y. Wong, B. Ahrén, C. J. M. Lips, J. W. M. Höppener, and F. Sundler, “Postnatally disturbed pancreatic islet cell distribution in human islet amyloid polypeptide transgenic mice,” Regulatory Peptides, vol. 113, no. 1–3, 89 pages, 2003.
- N. Wierup, M. J. Kuhar, B. O. Nilsson, H. Mulder, E. Ekblad, and F. Sundler, “Cocaine- and amphetamine-regulated transcript (CART) is expressed in several islet cell types during rat development,” Journal of Histochemistry & Cytochemistry, vol. 52, no. 2, 169 pages, 2004.
- B. J. de Haan, M. M. Faas, H. Spijker, J. W. van Willigen, A. de Haan, and P. de Vos, “Factors influencing isolation of functional pancreatic rat islets,” Pancreas, vol. 29, no. 1, e15 pages, 2004.
- P. T. R. van Suylichem, G. H. J. Wolters, and R. van Schilfgaarde, “The efficacy of density gradients for islet purification: a comparison of seven density gradients,” Transplant International, vol. 3, no. 3, 156 pages, 1990.
- W. C. Soeller, J. Janson, S. E. Hart, et al., “Islet amyloid-associated diabetes in obese A(vy)/a mice expressing human islet amyloid polypeptide,” Diabetes, vol. 47, no. 5, 743 pages, 1998.
- M. Couce, L. A. Kane, T. D. O'Brien, et al., “Treatment with growth hormone and dexamethasone in mice transgenic for human islet amyloid polypeptide causes islet amyloidosis and -cell dysfunction,” Diabetes, vol. 45, no. 8, 1094 pages, 1996.
- E. J. P. de Koning, E. R. Morris, F. M. A. Hofhuis, et al., “Intra- and extracellular amyloid fibrils are formed in cultured pancreatic islets of transgenic mice expressing human islet amyloid polypeptide,” Proceedings of the National Academy of Sciences of the United States of America, vol. 91, no. 18, 8467 pages, 1994.
- B. Ahrén and A. J. W. Scheurink, “Marked hyperleptinemia after high-fat diet associated with severe glucose intolerance in mice,” European Journal of Endocrinology, vol. 139, no. 4, 461 pages, 1998.
- B. Ahrén, “Diurnal variation in circulating leptin is dependent on gender, food intake and circulating insulin in mice,” Acta Physiologica Scandinavica, vol. 169, no. 4, 325 pages, 2000.
- H. Ohsawa, A. Kanatsuka, T. Yamaguchi, H. Makino, and S. Yoshida, “Islet amyloid polypeptide inhibits glucose-stimulated insulin secretion from isolated rat pancreatic islets,” Biochemical and Biophysical Research Communications, vol. 160, no. 2, 961 pages, 1989.
- A. Ar'Rajab and B. Ahrén, “Effects of amidated rat islet amyloid polypeptide on glucose-stimulated insulin secretion in vivo and in vitro in rats,” European Journal of Pharmacology, vol. 192, no. 3, 443 pages, 1991.
- B. Leighton and G. J. Cooper, “Pancreatic amylin and calcitonin gene-releted peptide cause resistance to insulin in skeletal muscle in vitro,” Nature, vol. 335, no. 6191, 632 pages, 1988.
- R. O. Deems, R. W. Deacon, and D. A. Young, “Amylin activates glycogen phosphorylase and inactivates glycogen synthase via a cAMP-independent mechanism,” Biochemical and Biophysical Research Communications, vol. 174, no. 2, 716 pages, 1991.
- J. M. Molina, G. J. S. Cooper, B. Leighton, and J. M. Olefsky, “Induction of insulin resistance in vivo by amylin and calcitonin gene-related peptide,” Diabetes, vol. 39, no. 2, 260 pages, 1990.
- J. P. H. Wilding, N. Khandan-Nia, W. M. Bennet, et al., “Lack of acute effect of amylin (islet associated polypeptide) on insulin sensitivity during hyperinsulinaemic euglycaemic clamp in humans,” Diabetologia, vol. 37, no. 2, 166 pages, 1994.
- T. P. Ciaraldi, M. Goldberg, R. Odom, and M. Stolpe, “In vivo effects of amylin on carbohydrate metabolism in liver cells,” Diabetes, vol. 41, no. 8, 975 pages, 1992.
- T. W. Stephens, W. F. Heath, and R. N. Hermeling, “Presence of liver CGRP/amylin receptors in only nonparenchymal cells and absence of direct regulation of rat liver glucose metabolism by CGRP/amylin,” Diabetes, vol. 40, no. 3, 395 pages, 1991.
- B. Thorens, “Molecular and cellular physiology of GLUT-2, a high-Km facilitated diffusion glucose transporter,” International Review of Cytology, vol. 137, 209 pages, 1992.
- E. J. P. de Koning, J. J. G. van den Brand, V. L. Mott, et al., “Macrophages and pancreatic islet amyloidosis,” Amyloid, vol. 5, no. 4, 247 pages, 1998.