Research Article | Open Access
Effect of Storage Temperature on Key Functions of Cultured Retinal Pigment Epithelial Cells
Purpose. Replacement of the diseased retinal pigment epithelium (RPE) with cells capable of performing the specialized functions of the RPE is the aim of cell replacement therapy for treatment of macular degenerative diseases. A storage method for RPE is likely to become a prerequisite for the establishment of such treatment. Herein, we analyze the effect of storage temperature on key functions of cultured RPE cells. Methods. Cultured ARPE-19 cells were stored in Minimum Essential Medium at 4°C, 16°C, and 37°C for seven days. Total RNA was isolated and the gene expression profile was determined using DNA microarrays. Comparison of the microarray expression values with qRT-PCR analysis of selected genes validated the results. Results. Expression levels of several key genes involved in phagocytosis, pigment synthesis, the visual cycle, adherens, and tight junctions, and glucose and ion transport were maintained close to control levels in cultures stored at 4°C and 16°C. Cultures stored at 37°C displayed regulational changes in a larger subset of genes related to phagocytosis, adherens, and tight junctions. Conclusion. RPE cultures stored at 4°C and 16°C for one week are capable of maintaining the expression levels of genes important for key RPE functions close to control levels.
The retinal pigment epithelium (RPE) is a highly specialized tissue. Situated between the neuroretina and choroid, it performs several functions that are crucial for supporting sight. Among the most important are phagocytosis of shed photoreceptor (PR) outer segments, regeneration of the visual cycle pigment rhodopsin, transportation of glucose and nutrients from the choroid to the distal part of the neuroretina, and transportation of excess fluid in the opposite direction [1, 2]. Malfunction of the RPE, implying a disrupted ability to perform these tasks, is a direct cause of prevalent retinal diseases like age-related macular degeneration (AMD) [3, 4] and a consequence of inherited disorders like Stargardt disease .
A promising approach for treatment of these diseases is the transplantation of tissue engineered RPE [6–10]. However, for the prospect of tissue engineering to become a widespread treatment option, it is necessary to ensure cell availability during short-term storage and transportation of RPE cells. In the process of establishing such a protocol, our research group has demonstrated that storage temperature has a crucial impact on the viability and morphology of cultured RPE cells . ARPE-19 cultures stored at 16°C displayed the greatest number of viable cells compared to cells stored at eight other temperatures (4°C, 8°C, 12°C, 20°C, 24°C, 28°C, 32°C, and 37°C) after seven days of storage .
Having established the potential effect of storage temperature on cell viability, we herein aim to investigate the effect of storage temperature on the gene expression associated with many highly specialized functions of the RPE, using microarray technology. Increased knowledge of the effects of storage on cultured ARPE-19 cells is imperative for future use of RPE transplantation in treatment of eye diseases affecting millions of people worldwide .
2. Materials and Methods
2.1. Cell Culture Media and Reagents
Adult retinal pigment epithelial cells (ARPE-19) were purchased from the American Type Culture Collection (ATCC) (Manassas, VA). Dulbecco’s Modified Eagle’s Medium (DMEM), Nutrient Mixture F12, fetal bovine serum (FBS), trypsin-EDTA, phosphate-buffered saline (PBS), 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), sodium bicarbonate, gentamycin, penicillin, and streptomycin were from Sigma-Aldrich (St. Louis, MO). Minimum Essential Medium (MEM) was purchased from Invitrogen (Carlsbad, CA). Nunclon T25 and T75 flasks, pipettes, and other routine plastics were purchased from VWR (West Chester, PA). The miRNeasy Mini Kit containing the QIAzol Lysis Reagent was obtained from Qiagen (Venlo, Netherlands).
2.2. Cell Culture and Storage
RPE cells from the ARPE-19 cell line were cultured under standard conditions in 95% air and 5% CO2 at 37°C in DMEM/F12 medium containing 10% FBS, 50 units/mL penicillin, and 50 μg/mL streptomycin. All ARPE-19 cells were from passage 4 and lower after acquisition from the vendor. Upon reaching confluence, the cells were seeded (5000 cells/cm2) in Nunclon T25 and T75 flasks. The culture medium was changed after two days, and confluent cultures were obtained on the third day. Three cultures were immediately processed for mRNA amplification and used as controls, while nine cultures were prepared for storage. The cells were rinsed with PBS, and the culture medium was replaced by storage medium consisting of MEM, 25 mM HEPES, 22.3 mM sodium bicarbonate, and 50 μg/mL gentamycin, hereafter referred to as MEM. The cultures were then placed in storage containers maintaining a stable temperature of either 4°C, 16°C, or 37°C and stored for seven days. The configuration and design of the custom-made storage containers have been explained earlier .
2.3. RNA Extraction and Microarray Hybridization
Cultured ARPE-19 cells that had been stored for seven days at 4°C, 16°C, and 37°C, as well as control cultures that had not been stored, were rinsed with PBS and directly lysed with QIAzol Lysis Reagent. 150 ng of total RNA was subjected to GeneChip HT One-Cycle cDNA Synthesis Kit and GeneChip HT IVT Labeling Kit, following the manufacturer’s protocol for whole genome gene expression analysis (Affymetrix, Santa Clara, CA, USA). Microarray analyses were performed using the Affymetrix GeneChip Human Gene 1.0 ST Arrays (Affymetrix, Santa Clara, CA), which contains approximately 28,000 gene transcripts. Biotinylated and fragmented single stranded cDNAs were hybridized to the GeneChips. The arrays were washed and stained using FS-450 fluidics station (Affymetrix). Signal intensities were detected by Hewlett Packard Gene Array Scanner 3000 7G (Hewlett Packard, Palo Alto, CA, USA).
The scanned images were processed using the AGCC (Affymetrix GeneChip Command Console) software and the CEL files were imported into Partek Genomics Suite software (Partek, Inc. MO, USA). The Robust Multichip Analysis (RMA) algorithm was applied for generation of signal values and normalization. Gene transcripts with maximal signal values of less than 32 across all arrays were removed to filter for low and nonexpressed genes, reducing the number of gene transcripts to 17,684. For expression comparisons of different groups, profiles were compared using a 1-way ANOVA model. The results were expressed as fold changes (FC) and values.
2.4. Microarray Data Analysis
Gene networks and canonical pathways representing key genes were identified using Ingenuity Pathways Analysis (IPA) (http://www.ingenuity.com/). Briefly, the data set containing gene identifiers and corresponding fold changes and values was uploaded into the web-delivered application and each gene identifier was mapped into its corresponding gene object in the Ingenuity Pathways Knowledge Base (IPKB). The functional analysis identified the biological functions and/or diseases that were most significant to the data sets. Fisher’s exact test was performed to calculate a value determining the probability that each biological function and/or disease assigned to the data set was due to chance alone. The data sets were mined for significant pathways with the IPA library of canonical pathways and networks were generated by using IPA as graphical representations of the molecular relationships between genes and gene products.
The presentation of the microarray data was divided into two manuscripts: the present and another addressing the genes not presented herein. This was done to allow for a more profound discussion of our findings.
2.5. Validation by PCR
The differential gene expression data were validated for selected transcripts (TYRP1, DSC1, and GLUT12) using TaqMan Gene Expression Assays and the Applied Biosystems ViiA 7 real-time PCR system (Applied Biosystems, Life Technologies). Briefly, 200 ng of total RNA was reverse transcribed using qScript cDNA Super Mix (Quanta Biosciences) following the manufacturer’s instructions. After completion of cDNA synthesis, 1/10th of the first strand reaction was used for PCR amplification. A total of 9 μL of diluted cDNA (diluted in H2O), 1 μL of selected primer/probes TaqMan Gene Expression Assays (Life Technologies), and 10 μL TaqMan Universal Master Mix (Life Technologies) were used following the manufacturer’s instructions. Transducin-like enhancer of split 1 (TLE1) was used as endogenous control due to low coefficient of variation (CV) (0.444) in the Affymetrix study. Each gene was run in duplicates. TaqMan Gene Expression Assays (Life Technology) used assays detecting TYRP1 (Hs00167051_m1), DSC1 (Hs00245189_m1), GLUT12 (Hs01547015_m1), and TLE1 (Hs00270768_m1).
values were calculated using Student’s -test in Microsoft Excel using delta Ct values. Normalized target gene expression levels (FC) were calculated using the formula: .
3.1. Analysis of Retinal Pigment Epithelial Cell Functions
In order to elucidate the expression patterns of genes critical to important RPE functions, we investigated the expression levels of individual genes associated with distinctive cellular properties (i.e., phagocytosis, pigment synthesis, visual cycle, adherens and tight junctions, and glucose and ion transport). Only significantly regulated genes are mentioned, namely, those displaying a value below 0.05. Results are presented in Table 1 and Figures 1-2.
| values < 0.05 are marked in bold font.|
Phagocytosis. Phagocytosis of photoreceptor (PR) outer segments is a crucial function of the RPE, and the components of its phagocytic machinery have been thoroughly described . Compared to control cells, cells that had been stored at 4°C and 16°C showed no difference in levels of expression for any of the 16 identified genes important for phagocytic functions. Cells that had been stored at 37°C displayed significant changes in gene regulation of several genes; however, only the engulfment-related gene PROS1 displayed a fold change of more than 1.5.
Pigment Synthesis. Production of melanin pigment by the RPE has two important functions in vivo: photoprotection, due to the antioxidant effect of melanin, and prevention of internal reflection of light from the sclera back to the retina . Of six identified genes related to pigment synthesis, SLC45A2 showed a 1.4-fold increase and MITF a 2.3-fold decrease in expression at 16°C compared to controls. TYRP1 showed a notable 3.6-fold upregulation at 37°C compared to control cells. At 4°C there were no significant differences in expression levels.
Visual Cycle. The RPE serves a crucial function in the visual cycle by reisomerizing all-trans-retinal to 11-cis-retinal, and defects in key proteins of the cycle can in themselves lead to various retinal diseases [1, 15]. Most of the identified visual cycle genes were maintained at expression levels similar to controls. RLBP1 and RBP7 expression was decreased 1.3-fold and 1.6-fold, respectively, in cells stored at 37°C, while RDH11 was decreased 1.2-fold in cells stored at 4°C. In cultures stored at 16°C, CRABP2 (RBP6) expression was increased 1.8-fold.
Adherens Junctions. Adherens junctions link actin filaments between epithelial cells and provide a strong mechanical attachment in cellular monolayers. Cadherins form homodimers with cadherins of adjacent cells and are pivotal for the integrity of the junction . A total of 13 different cadherins were identified in our data set, and their expression levels were unchanged in cells stored at 4°C and 16°C compared to the control. At 37°C, cadherins 6, 10, and 11 were downregulated 3.0-fold, 1.7-fold, and 2.2-fold, respectively, while DSC1 and CDH13 were upregulated 8.3-fold and 2.0-fold, respectively, compared to control cells.
Tight Junctions. Tight junctions of the RPE regulate cell polarity, proliferation, and paracellular diffusion, and they are constituents of the blood-retinal barrier . Of the 23 identified genes involved in the tight junction complex, seven were differentially expressed in cells stored at 16°C, but only the downregulation of MAGI1 and MAGI3 exceeded a fold change of 1.5. A total of 14 genes were differentially expressed at 37°C, of which CLDN11, F11R, and RAB3B were downregulated more than 1.5-fold. CRB3 was increased 1.2-fold in cells stored at 4°C.
Glucose Transport. The RPE is critical for supplying the inner part of the retina with glucose, and the maintenance and regulation of GLUT channels are essential for this function [18, 19]. In cells that had been stored at 16°C, we found an increased expression of three of a total of 11 glucose transporter isoforms identified in our material. GLUT3 was increased 2-fold, GLUT8 1.2-fold, and GLUT14 1.6-fold. In cells stored at 37°C, there was a 1.2-fold increase in expression of GLUT8 and a 2.7-fold decrease of GLUT12. No changes in expression were detected at 4°C.
Ion Transport. The Na-K-ATPase establishes and maintains electrochemical gradients across the plasma membrane , thereby providing the energy for transepithelial transport . Of six identified genes involved in the Na-K-ATPase, ATP1A3 and ATP1B2 were upregulated 1.4-fold and 1.2-fold at 16°C storage, respectively. ATP1A1 and ATP1B3 were upregulated 1.2-fold and 1.5-fold, respectively, at 37°C storage. There were no significant changes at 4°C compared to controls.
3.2. PCR Validation of Key Genes
Relative quantification of a few key genes (TYRP1, DSC1, and GLUT12) was performed with real-time PCR (Figure 3). The expression of TYRP1 was significantly upregulated to 8.2-fold at 37°C compared to controls. In comparison, the microarray data showed a 3.6-fold upregulation of this gene at 37°C. DSC1 expression was significantly and considerably upregulated in the 37°C group compared to controls, with a 67.0-fold upregulation. This is higher than the corresponding microarray data, which yielded an 8.3-fold upregulation at this temperature. PCR analysis of GLUT12 expression showed a similar downregulation compared to microarray results (3.0-fold and 2.7-fold, resp.). However, results were nonsignificant in the PCR group ( value = 0.068). PCR validation showed that expression of TYRP1, DSC1, and GLUT12 was not significantly regulated in the 4°C and 16°C culture groups, which is in line with the microarray data.
In this study, we investigated the effect of storage temperature on important cellular functions of ARPE-19 cells by comparing the expression levels of genes associated with phagocytosis, pigment synthesis, visual cycle, adherens and tight junctions, and glucose and ion transport.
The ARPE-19 cell line is recognized for displaying significant functional differentiation and forming polarized epithelial monolayers and tight junctions with barrier properties [21, 22]. However, the cell line does not mirror all the functions and characteristics of native RPE [23–25]. Some studies have demonstrated a relatively lower expression of some RPE-specific transcripts in ARPE-19 cells compared to native RPE cells , while others have not . Native RPE exhibits considerable regional variation, and thus any culture models will be inherently heterogeneous [23, 28, 29]. Cells and cell lines in culture can exceed the normal variation described in RPE in vivo [23, 30–32]. Gene expression by cultured RPE cells is substrate dependent , and ARPE-19 grown on plastic displays the phenotype closest to native RPE, capable of yielding a functional profile of differentially expressed genes . The global expression profile of ARPE-19 cells can also be directed towards that of primary RPE cells by withdrawing serum . In the present study, cells were cultured and stored on plastic, and the storage medium contained no xenobiotic components.
Phagocytosis of shed photoreceptor outer segments is vital to photoreceptor repair and represents one of the most critical functions of the RPE [1, 35]. We found no changes in expression of phagocytosis-associated genes after storage at 4°C and 16°C compared to control cells (Table 1). Two receptor ligand pairs are recognized for exhibiting key roles in the molecular machinery of RPE phagocytosis. These include the receptor tyrosine kinase MerTK and its secreted ligands Gas6 and Protein S, as well as the integrin receptor αVβ5 and its secreted ligand MFG-E8 . ARPE-19 cells are capable of phagocytosing photoreceptor outer segments [37–39], but some differences exist compared to primary cultures. Both require the integrin receptor αvβ5 for the binding and internalization of outer segments [21, 37], the main difference being observed at the level of promoter strength, yielding much higher transcriptional activity in ARPE-19 . With the exception of Protein S, expression of all of these important genes was maintained during storage at all temperatures. Although the differences in expression of the remaining phagocytosis associated genes were modest, these results may indicate a slightly disrupted phagocytic ability in cells stored at 37°C.
The expression of genes associated with pigment synthesis in the RPE was also evaluated due to its many functions, including protection from oxidative stress [41–43]. Four genes have been described as key contributors in the melanin biosynthesis pathway: TYR, TYRP1, TYRP2, and P gene (OCA2) . Smith-Thomas et al.  found that primary human RPE cells failed to express TYRP2 and that a very low percentage of the cells expressed TYRP1, but only if cultured for more than 3 weeks. Lu et al.  found that human RPE cultured under standard conditions failed to express any of the four key genes mentioned above. However, we were able to detect both OCA2 and TYRP1 in all culture groups, as well as several other genes related to pigment synthesis (Table 1).
Upon transduction of light energy into electrical impulses in the PR, 11-cis-retinal is converted to all-trans-retinal, which is cycled to the RPE for reisomerization . A string of proteins contributes in the visual cycle, and the expression levels of critically important proteins such as cellular retinol binding protein 1 (RBP1, also known as CRBP1), lecithin retinol acyltransferase (LRAT), cellular retinaldehyde binding protein 1 (RLBP1, also referred to as CRALBP), and cellular retinol binding protein 5 (RBP5) were maintained at control levels during storage at all three temperatures. This indicates that the visual cycle can be preserved under the storage conditions used in this study.
Cell-cell adhesion is important for maintaining the correct RPE phenotype [45, 46]. Cultures stored at 4°C and 16°C did not differ from controls in regard to expression of adherens junction genes. Cultures stored at 37°C, however, showed a differential regulation of five adherens junction genes, among them an 8.3-fold upregulation of DSC1 and a change in expression of several cadherins. These changes might indicate a slight perturbance of adherens junction properties after 37°C storage. This group also showed the largest expression changes of tight junction genes, mostly downregulation. This might indicate a loss of integrity of the intercellular junction in cells stored at 37°C compared to control cells. The classic tight junction proteins ZO-1 and occludin did not display any changes in expression levels after storage at any of the three temperatures.
In a previous study, we demonstrated that the number of viable ARPE-19 cells at 4°C storage dropped to less than 4% compared to the control group . In the present study, we find few differences between the 4°C group and the control. This seemingly contradictory finding can have at least two explanations. First, the cultures stored at 4°C contain a large number of dead and dying cells, which have a tendency to detach and be washed away during preparations, thereby not being included in the analysis. Second, temperature has a crucial effect on the adhesive abilities of several cell types [47–50] and adhesion seems to be severely affected during 4°C storage, resulting in the loss of otherwise viable and well-functioning cells from the monolayer. Unpublished data from our research group demonstrates improved viability following storage at 4°C by implementing a radical change in the culture protocol in order to improve cell adhesion. This finding supports our hypothesis that cellular adhesion is severely affected at low storage temperatures.
We also assessed the expression of glucose and ion transporters. Several GLUT proteins were identified in our material, with GLUT1 expression being dominant (Table 1). This is in line with existing gene expression studies on native RPE [18, 51, 52]. Expression of GLUT1 was maintained at control levels during storage at all temperatures. Given the dominant role of this transporter in RPE cells, the maintenance of its expression in all storage groups indicates a preservation of glucose transport function after storage. In an earlier study by Takagi et al. , the addition of FBS to the culture medium was shown to increase the expression of GLUT1 in human RPE cells. Based on this observation, one might anticipate a downregulation of this isoform when replacing the FBS-containing growth medium with a xenobiotic-free storage medium. However, that was not the case in our cultures. Expression of GLUT3 was increased 2-fold after storage at 16°C. GLUT3 is highly effective, displaying both a higher affinity and a fivefold greater transport capacity for glucose than other isoforms including GLUT1 . Its expression has been identified in several cell types characterized by very specific and high metabolic demand, such as neurons and placental trophoblasts [53–55]. Its expression in neurons increases in an activity-related manner to meet an increased demand . We speculate whether this strategy is utilized by ARPE-19 cells stored at 16°C and if it contributes to preserving a larger number of viable cells compared to other temperatures where GLUT3 expression remains unchanged.
Active transport of Na+ across the apical membrane of RPE cells creates a high Na+ concentration in the subretinal space, which is crucial for the photoreceptor dark current and for transport of solutes through symporters and antiporters of the RPE . Three isoforms of each of the Na-K-ATPase α and β subunits were identified, and most were expressed close to control levels in all storage groups. The same isoforms were identified in a recent study on native RPE .
When comparing the expression levels of genes involved in important RPE functions, it is evident that cells stored at 37°C display expression changes in a larger number of genes than cells stored at 4°C and 16°C. In conclusion, the findings of this study show that cells stored at 4°C and 16°C are capable of maintaining expression levels of genes important for key RPE functions close to the control levels.
Conflict of Interests
The authors declare no conflict of interests.
The study has received funding from the Norwegian Research Council, the South-Eastern Norway Regional Health Authority, and the Norwegian Association of the Blind and Partially Sighted. The authors wish to thank Dr. Dong Feng Chen, Schepens Eye Research Institute, Harvard Medical School, for excellent help and support.
- J. R. Sparrrow, D. Hicks, and C. P. Hamel, “The retinal pigment epithelium in health and disease,” Current Molecular Medicine, vol. 10, no. 9, pp. 802–823, 2010.
- M. F. Marmor, “Control of subretinal fluid: experimental and clinical studies,” Eye, vol. 4, no. 1, pp. 340–344, 1990.
- P. T. V. M. de Jong, “Age-related macular degeneration,” The New England Journal of Medicine, vol. 355, no. 14, pp. 1474–1485, 2006.
- A.-J. F. Carr, M. J. K. Smart, C. M. Ramsden, M. B. Powner, L. da Cruz, and P. J. Coffey, “Development of human embryonic stem cell therapies for age-related macular degeneration,” Trends in Neurosciences, vol. 36, no. 7, pp. 385–395, 2013.
- S. Walia and G. A. Fishman, “Natural history of phenotypic changes in Stargardt macular dystrophy,” Ophthalmic Genetics, vol. 30, no. 2, pp. 63–68, 2009.
- C. M. Sheridan, S. Mason, D. M. Pattwell, D. Kent, I. Grierson, and R. Williams, “Replacement of the RPE monolayer,” Eye, vol. 23, no. 10, pp. 1910–1915, 2009.
- N. Yaji, M. Yamato, J. Yang, T. Okano, and S. Hori, “Transplantation of tissue-engineered retinal pigment epithelial cell sheets in a rabbit model,” Biomaterials, vol. 30, no. 5, pp. 797–803, 2009.
- R. D. Lund, P. Adamson, Y. Sauvé et al., “Subretinal transplantation of genetically modified human cell lines attenuates loss of visual function in dystrophic rats,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 17, pp. 9942–9947, 2001.
- P. J. Coffey, S. Girman, S. M. Wang et al., “Long-term preservation of cortically dependent visual function in RCS rats by transplantation,” Nature Neuroscience, vol. 5, no. 1, pp. 53–56, 2002.
- L. da Cruz, F. K. Chen, A. Ahmado, J. Greenwood, and P. Coffey, “RPE transplantation and its role in retinal disease,” Progress in Retinal and Eye Research, vol. 26, no. 6, pp. 598–635, 2007.
- L. Pasovic, T. P. Utheim, R. Maria et al., “Optimization of storage temperature for cultured ARPE-19 cells,” Journal of Ophthalmology, vol. 2013, Article ID 216359, 11 pages, 2013.
- A. Chopdar, U. Chakravarthy, and D. Verma, “Age related macular degeneration,” British Medical Journal, vol. 326, no. 7387, pp. 485–488, 2003.
- B. M. Kevany and K. Palczewski, “Phagocytosis of retinal rod and cone photoreceptors,” Physiology, vol. 25, no. 1, pp. 8–15, 2010.
- L. Smith-Thomas, P. Richardson, A. J. Thody et al., “Human ocular melanocytes and retinal pigment epithelial cells differ in their melanogenic properties in vivo and in vitro,” Current Eye Research, vol. 15, no. 11, pp. 1079–1091, 1996.
- O. Strauss, “The retinal pigment epithelium in visual function,” Physiological Reviews, vol. 85, no. 3, pp. 845–881, 2005.
- M. Kaida, F. Cao, C. M. B. Skumatz, P. E. Irving, and J. M. Burke, “Time at confluence for human RPE cells: effects on the adherens junction and in vitro wound closure,” Investigative Ophthalmology and Visual Science, vol. 41, no. 10, pp. 3215–3224, 2000.
- L. J. Rizzolo, “Development and role of tight junctions in the retinal pigment epithelium,” International Review of Cytology, vol. 258, pp. 195–234, 2007.
- Y. Ban and L. J. Rizzolo, “Regulation of glucose transporters during development of the retinal pigment epithelium,” Developmental Brain Research, vol. 121, no. 1, pp. 89–95, 2000.
- P. D. Senanayake, A. Calabro, J. G. Hu et al., “Glucose utilization by the retinal pigment epithelium: evidence for rapid uptake and storage in glycogen, followed by glycogen utilization,” Experimental Eye Research, vol. 83, no. 2, pp. 235–246, 2006.
- K. Geering, “Subunit assembly and functional maturation of Na,K-ATPase,” Journal of Membrane Biology, vol. 115, no. 2, pp. 109–121, 1990.
- K. C. Dunn, A. E. Aotaki-Keen, F. R. Putkey, and L. M. Hjelmeland, “ARPE-19, a human retinal pigment epithelial cell line with differentiated properties,” Experimental Eye Research, vol. 62, no. 2, pp. 155–169, 1996.
- K. C. Dunn, A. D. Marmorstein, V. L. Bonilha, E. Rodriguez-Boulan, F. Giordano, and L. M. Hjelmeland, “Use of the ARPE-19 cell line as a model of RPE polarity: basolateral secretion of FGF5,” Investigative Ophthalmology and Visual Science, vol. 39, no. 13, pp. 2744–2749, 1998.
- Y. Luo, Y. Zhuo, M. Fukuhara, and L. J. Rizzolo, “Effects of culture conditions on heterogeneity and the apical junctional complex of the ARPE-19 cell line,” Investigative Ophthalmology and Visual Science, vol. 47, no. 8, pp. 3644–3655, 2006.
- J. Tian, K. Ishibashi, S. Honda, S. A. Boylan, L. M. Hjelmeland, and J. T. Handa, “The expression of native and cultured human retinal pigment epithelial cells grown in different culture conditions,” British Journal of Ophthalmology, vol. 89, no. 11, pp. 1510–1517, 2005.
- P. Geisen, J. R. McColm, B. M. King, and M. E. Hartnett, “Characterization of barrier properties and inducible VEGF expression of several types of retinal pigment epithelium in medium-term culture,” Current Eye Research, vol. 31, no. 9, pp. 739–748, 2006.
- N. V. Strunnikova, A. Maminishkis, J. J. Barb et al., “Transcriptome analysis and molecular signature of human retinal pigment epithelium,” Human Molecular Genetics, vol. 19, no. 12, Article ID ddq129, pp. 2468–2486, 2010.
- H. Cai and L. V. Del Priore, “Gene expression profile of cultured adult compared to immortalized human retinal pigment epithelium,” Molecular Vision, vol. 12, pp. 1–14, 2006.
- J. M. Burke, F. Cao, and P. E. Irving, “High levels of E-/P-cadherin: correlation with decreased apical polarity of Na/K ATPase in bovine RPE cells in situ,” Investigative Ophthalmology and Visual Science, vol. 41, no. 7, pp. 1945–1952, 2000.
- J. M. Burke and L. M. Hjelmeland, “Mosaicism of the retinal pigment epithelium: seeing the small picture,” Molecular Interventions, vol. 5, no. 4, pp. 241–249, 2005.
- A. Ando, M. Ueda, M. Uyama, Y. Masu, T. Okumura, and S. Ito, “Heterogeneity in ornithine cytotoxicity of bovine retinal pigment epithelial cells in primary culture,” Experimental Eye Research, vol. 70, no. 1, pp. 89–96, 2000.
- B. S. Mckay and J. M. Burke, “Separation of phenotypically distinct subpopulations of cultured human retinal pigment epithelial cells,” Experimental Cell Research, vol. 213, no. 1, pp. 85–92, 1994.
- D. M. Albert, M. O. M. Tso, and A. S. Rabson, “In vitro growth of pure cultures of retinal pigment epithelium,” Archives of Ophthalmology, vol. 88, no. 1, pp. 63–69, 1972.
- R. K. Sharma, W. E. Orr, A. D. Schmitt, and D. A. Johnson, “A functional profile of gene expression in ARPE-19 cells,” BMC Ophthalmology, vol. 5, article 25, 2005.
- J. Tian, K. Ishibashi, and J. T. Handa, “The expression of native and cultured RPE grown on different matrices,” Physiological Genomics, vol. 17, no. 2, pp. 170–182, 2004.
- S. Binder, B. V. Stanzel, I. Krebs, and C. Glittenberg, “Transplantation of the RPE in AMD,” Progress in Retinal and Eye Research, vol. 26, no. 5, pp. 516–554, 2007.
- F. Mazzoni, H. Safa, and S. C. Finnemann, “Understanding photoreceptor outer segment phagocytosis: use and utility of RPE cells in culture,” Experimental Eye Research, vol. 126, pp. 51–60, 2014.
- S. C. Finnemann, V. L. Bonilha, A. D. Marmorstein, and E. Rodriguez-Boulan, “Phagocytosis of rod outer segments by retinal pigment epithelial cells requires αvβ5 integrin for binding but not for internalization,” Proceedings of the National Academy of Sciences of the United States of America, vol. 94, no. 24, pp. 12932–12937, 1997.
- E. U. Irschick, R. Sgonc, G. Böck et al., “Retinal pigment epithelial phagocytosis and metabolism differ from those of macrophages,” Ophthalmic Research, vol. 36, no. 4, pp. 200–210, 2004.
- E. U. Irschick, G. Haas, M. Geiger et al., “Phagocytosis of human retinal pigment epithelial cells: evidence of a diurnal rhythm, involvement of the cytoskeleton and interference of antiviral drugs,” Ophthalmic Research, vol. 38, no. 3, pp. 164–174, 2006.
- S. Proulx, S. Landreville, S. L. Guérin, and C. Salesse, “Integrin α5 expression by the ARPE-19 cell line: comparison with primary RPE cultures and effect of growth medium on the α5 gene promoter strength,” Experimental Eye Research, vol. 79, no. 2, pp. 157–165, 2004.
- S. Memoli, A. Napolitano, M. D'Ischia, G. Misuraca, A. Palumbo, and G. Prota, “Diffusible melanin-related metabolites are potent inhibitors of lipid peroxidation,” Biochimica et Biophysica Acta—Lipids and Lipid Metabolism, vol. 1346, no. 1, pp. 61–68, 1997.
- Z. Wang, J. Dillon, and E. R. Gaillard, “Antioxidant properties of melanin in retinal pigment epithelial cells,” Photochemistry and Photobiology, vol. 82, no. 2, pp. 474–479, 2006.
- U. Schraermeyer and K. Heimann, “Current understanding on the role of retinal pigment epithelium and its pigmentation,” Pigment Cell Research, vol. 12, no. 4, pp. 219–236, 1999.
- F. Lu, D. Yan, X. Zhou, D.-N. Hu, and J. Qu, “Expression of melanin-related genes in cultured adult human retinal pigment epithelium and uveal melanoma cells,” Molecular Vision, vol. 13, pp. 2066–2072, 2007.
- W. K. Jin, H. K. Kyung, P. Burrola, T. W. Mak, and G. Lemke, “Retinal degeneration triggered by inactivation of PTEN in the retinal pigment epithelium,” Genes & Development, vol. 22, no. 22, pp. 3147–3157, 2008.
- S. Tamiya, L. Liu, and H. J. Kaplan, “Epithelial-mesenchymal transition and proliferation of retinal pigment epithelial cells initiated upon loss of cell-cell contact,” Investigative Ophthalmology and Visual Science, vol. 51, no. 5, pp. 2755–2763, 2010.
- F. Rico, C. Chu, M. H. Abdulreda, Y. Qin, and V. T. Moy, “Temperature modulation of integrin-mediated cell adhesion,” Biophysical Journal, vol. 99, no. 5, pp. 1387–1396, 2010.
- G. Sagvolden, I. Giaever, E. O. Pettersen, and J. Feder, “Cell adhesion force microscopy,” Proceedings of the National Academy of Sciences of the United States of America, vol. 96, no. 2, pp. 471–476, 1999.
- E. B. Lomakina and R. E. Waugh, “Micromechanical tests of adhesion dynamics between neutrophils and immobilized ICAM-1,” Biophysical Journal, vol. 86, no. 2, pp. 1223–1233, 2004.
- R. L. Juliano and E. Gagalang, “The adhesion of Chinese hamster cells. I. Effects of temperature, metabolic inhibitors and proteolytic dissection of cell surface macromolecules,” Journal of Cellular Physiology, vol. 92, no. 2, pp. 209–220, 1977.
- Z. Zhang, Y. Zhang, H. Xiao, X. Liang, D. Sun, and S. Peng, “A gene expression profile of the developing human retinal pigment epithelium,” Molecular Vision, vol. 18, pp. 2961–2975, 2012.
- H. Takagi, H. Tanihara, Y. Seino, and N. Yoshimura, “Characterization of glucose transporter in cultured human retinal pigment epithelial cells: gene expression and effect of growth factors,” Investigative Ophthalmology and Visual Science, vol. 35, no. 1, pp. 170–177, 1994.
- I. A. Simpson, D. Dwyer, D. Malide, K. H. Moley, A. Travis, and S. J. Vannucci, “The facilitative glucose transporter GLUT3: 20 years of distinction,” American Journal of Physiology—Endocrinology and Metabolism, vol. 295, no. 2, pp. E242–E253, 2008.
- D. Z. Gerhart, M. A. Broderius, N. D. Borson, and L. R. Drewes, “Neurons and microvessels express the brain glucose transporter protein GLUT3,” Proceedings of the National Academy of Sciences of the United States of America, vol. 89, no. 2, pp. 733–737, 1992.
- M. Pantaleon, M. B. Harvey, W. S. Pascoe, D. E. James, and P. L. Kaye, “Glucose transporter GLUT3: ontogeny, targeting, and role in the mouse blastocyst,” Proceedings of the National Academy of Sciences of the United States of America, vol. 94, no. 8, pp. 3795–3800, 1997.
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