Isolation and characterization of a spontaneously immortalized bovine retinal pigmented epithelial cell line

作者: Thomas E Liggett , T Daniel Griffiths , Elizabeth R Gaillard

DOI: 10.1186/1471-2121-10-33

关键词:

摘要: The Retinal Pigmented Epithelium (RPE) is juxtaposed with the photoreceptor outer segments of eye. proximity cells a prerequisite for their survival, as they depend on RPE to remove and are also influenced by cell paracrine factors. death can cause progressive loss function, which diminish vision and, over time, blindness ensues. Degeneration retina has been shown induce variety retinopathies, such Stargardt's disease, Cone-Rod Dystrophy (CRD), Retinitis Pigmentosa (RP), Fundus Flavimaculatus (FFM), Best's disease Age-related Macular (AMD). We have cultured primary bovine gain further understanding mechanisms death. One cultures, named tRPE, surpassed senescence was characterized determine its viability model retinal diseases. tRPE line passaged up 150 population doublings be morphologically similar cells. They origin reverse transcriptase PCR immunocytochemistry using RPE-specific genes RPE65 CRALBP proteins Bestrophin. immunoreactive vimentin, cytokeratin zonula occludens-1 antibodies. Chromosome analysis indicates normal diploid number. do not grow in suspension or soft agar. After 3H thymidine incorporation, appear divide appreciably after confluency. immortal, but still exhibit contact inhibition, serum dependence, monolayer growth secrete an extra-cellular matrix. retain in-vivo morphology, gene expression polarity. Additionally, endocytose exogenous melanin, A2E purified lipofuscin granules. This may useful in-vitro research maculopathies.

参考文章(82)
P S Bernstein, R C Hunt, A A Davis, J Turner, M Nachtigal, D Bok, A human retinal pigment epithelial cell line that retains epithelial characteristics after prolonged culture. Investigative Ophthalmology & Visual Science. ,vol. 36, pp. 955- 964 ,(1995)
T. Michael Redmond, Martin L. Katz, Effect of Rpe65 knockout on accumulation of lipofuscin fluorophores in the retinal pigment epithelium. Investigative Ophthalmology & Visual Science. ,vol. 42, pp. 3023- 3030 ,(2001)
Christine M. B. Skumatz, Feng Cao, Janice M. Burke, Pamela E. Irving, Mayumi Kaida, Time at confluence for human RPE cells: effects on the adherens junction and in vitro wound closure. Investigative Ophthalmology & Visual Science. ,vol. 41, pp. 3215- 3224 ,(2000)
David Hicks, Ruben Adler, Fulton Wong, Donald Price, Christine Curcio, Cell death in age-related macular degeneration. Molecular Vision. ,vol. 5, pp. 31- ,(1999)
Maurice F. Rabb, Mark O.M. Tso, Gerald A. Fishman, Cone-Rod Dystrophy Ophthalmology. ,vol. 93, pp. 1443- 1451 ,(1986) , 10.1016/S0161-6420(86)33547-4
P A Campochiaro, S F Hackett, B P Conway, Retinoic acid promotes density-dependent growth arrest in human retinal pigment epithelial cells. Investigative Ophthalmology & Visual Science. ,vol. 32, pp. 65- 72 ,(1991)
Leonard M. Hjelmeland, Behnom Farboud, James T. Handa, Shigeru Honda, Induction of an aging mRNA retinal pigment epithelial cell phenotype by matrix-containing advanced glycation end products in vitro. Investigative Ophthalmology & Visual Science. ,vol. 42, pp. 2419- 2425 ,(2001)
Feeney-Burns L, Eldred Ge, The fate of the phagosome: conversion to 'age pigment' and impact in human retinal pigment epithelium. Transactions of the ophthalmological societies of the United Kingdom. pp. 416- ,(1983)
Toshinari Minamoto, Yasuhiko Tanaka, Kazuteru Kigasawa, Hiroshi Ishikawa, Hajime Obazawa, Yutaka Nagai, Collagen production by cultured human retinal pigment epithelial cells. The Tokai journal of experimental and clinical medicine. ,vol. 23, pp. 147- 151 ,(1998)
Debra A. Thompson, Kazuhide Kawase, Aileen Nicoletti, Promoter analysis of RPE65, the gene encoding a 61-kDa retinal pigment epithelium-specific protein Investigative Ophthalmology & Visual Science. ,vol. 39, pp. 637- 644 ,(1998)