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Heterogeneidade das células do epitélio pigmentado da retina na expressão do complexo principal de histocompatibilidade - II (CPH-II) após estimulação com lnterferon-γ

Heterogeneidade das células do epitélio pigmentado da retina na expressão do complexo principal de histocompatibilidade - II (CPH-II) após estimulação com lnterferon-γ

Autores:

Antonio Marcelo Barbante Casella,
Michel Eid Farah,
Katia Emiko Taba,
Stephen J. Ryan

ARTIGO ORIGINAL

Arquivos Brasileiros de Oftalmologia

versão impressa ISSN 0004-2749versão On-line ISSN 1678-2925

Arq. Bras. Oftalmol. vol.61 no.1 São Paulo fev. 1998

http://dx.doi.org/10.5935/0004-2749.19980113

SUMMARY

Pupose:

To evaluate the pattern of expression of MHC Class II in vitro in human retinal pigment epithelium (RPE) explant cultures treated with interferon-gamma (IFN-γ), and in vivo in rabbit RPE after subretinal injection of IFN-γ.

Methods:

Class II expression was studied on RPE by immunohistochemistry in explant cultures of 6 adult human eyes (all over 70 years), 4 fetal human eyes, and in 12 albino rabbit eyes. The human explants were stimulated with IFN-γ (50 U/ml) for 72 hours prior to immunostaining for Class II. The rabbit eyes were injected in vivo subretinally with 500 U of IFN-γ and analyzed immunohistochemically 3 days later.

Results:

A heterogeneous pattern of Class II expression was present on IFN-γ stimulated RPE in both in vivo and in vitro experiments. In aged human eyes the percent of Class-II positive cells was higher in the periphery than the posterior pole (macular region) (P<0.01), however there was no such difference in the fetal eyes.

Conclusion:

RPE cells are heterogeneous in their expression of HLA Class II after stimulation with IFN-γ in both in vitro and in vivo studies. Regional differences in Class II are seen in aged human eyes but not in fetal human eyes. This study provides evidence of functional heterogeneity of RPE and it is supportive of previous studies demonstrating phenotypic RPE heterogeneity.

REFERÊNCIAS

1 Barreau E, Brossas JY, Coutois Y, Treton JA. Accumulation of mitochondrial DNA deletions in human retina during aging. lnvest Ophthalmol Vis Sci 1996;37:384-91.
2 Baudouin C, Brinole F, Bayle J, Fredj-Reygrobellet D, Lapalus P, Gastaud P. Class II histocompatibility antigen expression by cellular components of vitreous and subretinal fluid in proliferative vitreoretinopathy. Invest Ophthalmol Vis Sci 1991;32:2065-72.
3 Burke JM, Mekay BS. In vitro aging of bovine and human rutural pigment epithelium: number and activity of the Na/K ATPase pump. Exp Eye Res 1993;57:51-57.
4 Burke JM, Skumatz CMB, lrving PE, Maekay B. Phenotypic heterogeneity of retinal pigment epithelial cells in vitro and in situ. Exp Eye Res 1996; 62:63-73.
5 Cabral L, Unger W, Boulton M, Lighfoot R, MeKeehnie N, Grierson I, Marshall J. Regional distribution of lysossomal enzymes in the canine retinal pigment epithelium. Invest Ophthalmol Vis Sci 1990;31:670-6.
6 Chan CC, Detriek B, Nussemblat RB, Palestine AG, Fujikawa LS, Hooks JJ. HLA-DR antigens on retinal pigment epithelial cells from patients with uveitis. Areh Ophthalmol 1986;104:725-9.
7 Gao H, Hollyfield JG. Aging of the human retina. Invest Ophthalmol Vis Sci 1992;33: 1-17.
8 Maclaren MJ - Kinetics of rod outer segment phagocytoses by cultered retinal pigment epithelial cells. Invest Ophthalmol Vis Sci 1996;34:3068-75.
9 Percopo Cm, Hooks JJ, Shinohara T, Caspi R, Detriek B. Cytokine-mediated activation of a neuronal retinal resident cell provokes antigen presentation. Journal of Immunology 1990;145:4101-7.
10 Yamamot S, Du J, Gouras P, Kjeldyett H. Retinal pigment epithelial transplants and retinal function nin RCS rats. Invest Ophthalmol Vis Sci 1993;34:3068-75.
11 Waekefield D, Lloyde A. The role of cytokines in the pathogeneis of inflammatory eye disease. Cytokine 1992;4:1-5.
12 Wiedemann P. Growth factors in retinal diseases: proliferative vitreoretinopathy, proliferative diabetic retinopathy and retinal degeneration. Surv Ophthalmol 1992;36:373-84.