Retinoic acid signaling in mammalian eye development

被引:152
作者
Cvekl, Ales [1 ,2 ]
Wang, Wei-Lin [1 ]
机构
[1] Albert Einstein Coll Med, Dept Genet, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Ophthalmol & Visual Sci, Bronx, NY 10461 USA
关键词
anterior segment; lens; nuclear receptors; periocular mesenchyme; optic cup; retina; retinoic acid; vitamin A; THYROID-HORMONE RECEPTOR; CRYSTALLIN GENE-EXPRESSION; CREB-BINDING PROTEIN/P300; DEVELOPING MOUSE RETINA; UNION-OF-PHARMACOLOGY; ALPHA-B-CRYSTALLIN; VITAMIN-A TOXICITY; NULL MUTANT MICE; NUCLEAR RECEPTOR; RESPONSE ELEMENT;
D O I
10.1016/j.exer.2009.04.012
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Retinoic acid (RA) is a biologically active metabolite of vitamin A (retinol) that serves as a signaling molecule during a number of developmental and physiological processes. RA signaling plays multiple roles during embryonic eye development RA signaling is initially required for reciprocal interactions between the optic vesicle and invaginating lens placode. RA signaling promotes normal development of the ventral retina and optic nerve through its activities in the neural crest cell-derived periocular mesenchyme. RA coordinates these processes by regulating biological activities of a family of non-steroid hormone receptors, RAR alpha/beta/gamma, and RXR alpha/beta/gamma. These DNA-binding transcription factors recognize DNA as RAR/RXR heterodimers and recruit multiprotein transcriptional co-repressor complexes. RA-binding to RAR receptors induces a conformational change in the receptor, followed by the replacement of co-repressor with co-activator complexes. Inactivation of RAR alpha/beta/gamma receptors in the periocular mesenchyme abrogates anterior eye segment formation. This review summarizes recent genetic studies of RA signaling and progress in understanding the molecular mechanism of transcriptional co-activators that function with RAR/RXR. (c) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:280 / 291
页数:12
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