Expression of the candidate circadian photopigment melanopsin (Opn4) in the mouse retinal pigment epithelium

被引:48
作者
Peirson, SN
Bovee-Geurts, PHM
Lupi, D
Jeffery, G
DeGrip, WJ
Foster, RG
机构
[1] Charing Cross Hosp, Imperial Coll London, Fac Med, Div Neurosci & Psychol Med,Dept Visual Neurosci, London W6 8RF, England
[2] Univ Nijmegen, NCMLS, Dept Biochem, Nijmegen, Netherlands
[3] UCL, Inst Ophthalmol, Dept Visual Sci, London EC1V 9EL, England
来源
MOLECULAR BRAIN RESEARCH | 2004年 / 123卷 / 1-2期
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
Opn4; melanopsin; RPE; circadian; photopigment;
D O I
10.1016/j.molbrainres.2004.01.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A number of responses to light, including circadian entrainment and pupillary constriction, are preserved in mammals that lack rod and cone photoreceptors. Recent studies have demonstrated that a subset of retinal ganglion cells (RGCs) are intrinsically photosensitive, and that these RGCs project to regions of the brain associated with the regulation of the circadian clock and pupil constriction. The photopigment gene(s) that mediate these effects of irradiance remain unidentified, although melanopsin (Opn4) has emerged as a strong candidate. For example, Opn4 is expressed within intrinsically photosensitive RGCs, and Opn4 knock-out mice show attenuated circadian and pupillary responses to light. In this study we provide the first clear evidence that Opn4 expression is not confined to these photosensitive RGCs, but is also expressed in the retinal pigment epithelium (RPE), a tissue with no known photosensensory role. We can preclude retinal contamination of RPE extracts as levels of Opn4 expression were higher in the RPE than in the retina, and the expression of rod opsin and Thy1 (a marker of the RGC layer) were barely detectable in RPE extracts. Our results raise questions about the presumed function of melanopsin, and highlight the need for biochemical studies on this protein. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:132 / 135
页数:4
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