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Collagen XVIII/endostatin is essential for vision and retinal pigment epithelial function
Author(s) -
Marneros Alexander G,
Keene Douglas R,
Hansen Uwe,
Fukai Naomi,
Moulton Karen,
Goletz Patrice L,
Moiseyev Gennadiy,
Pawlyk Basil S,
Halfter Willi,
Dong Sucai,
Shibata Masao,
Li Tiansen,
Crouch Rosalie K,
Bruckner Peter,
Olsen Bjorn R
Publication year - 2004
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1038/sj.emboj.7600014
Subject(s) - biology , retinal , pigment , endostatin , retinal pigment epithelium , microbiology and biotechnology , biochemistry , genetics , angiogenesis , chemistry , organic chemistry
Age‐related macular degeneration (ARMD) with abnormal deposit formation under the retinal pigment epithelium (RPE) is the major cause of blindness in the Western world. basal laminar deposits are found in early ARMD and are composed of excess basement membrane material produced by the RPE. Here, we demonstrate that mice lacking the basement membrane component collagen XVIII/endostatin have massive accumulation of sub‐RPE deposits with striking similarities to basal laminar deposits, abnormal RPE, and age‐dependent loss of vision. The progressive attenuation of visual function results from decreased retinal rhodopsin content as a consequence of abnormal vitamin A metabolism in the RPE. In addition, aged mutant mice show photoreceptor abnormalities and increased expression of glial fibrillary acidic protein in the neural retina. Our data demonstrate that collagen XVIII/endostatin is essential for RPE function, and suggest an important role of this collagen in Bruch's membrane. Consistent with such a role, the ultrastructural organization of collagen XVIII/endostatin in basement membranes, including Bruch's membrane, shows that it is part of basement membrane molecular networks.