Development and diversification of retinal amacrine interneurons at single cell resolution

被引:92
作者
Cherry, Timothy J. [1 ]
Trimarchi, Jeffrey M. [1 ]
Stadler, Michael B. [2 ]
Cepko, Constance L. [1 ,3 ,4 ]
机构
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[2] Friedrich Miescher Inst Biomed Res, CH-4058 Basel, Switzerland
[3] Harvard Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Dept Ophthalmol, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
amacrine cell; neuronal classification; retinal development; single cell profiling; molecular taxonomy; IN-VIVO; EXPRESSION; TRANSCRIPTOME; GENESIS;
D O I
10.1073/pnas.0903264106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The vertebrate retina uses diverse neuronal cell types arrayed into complex neural circuits to extract, process, and relay information from the visual scene to the higher order processing centers of the brain. Amacrine cells, a class of interneurons, are thought to mediate much of the processing of the visual signal that occurs within the retina. Although amacrine cells display extensive morphological diversity, the molecular nature of this diversity is largely unknown. Furthermore, it is not known how this diversity arises during development. Here, we have combined in vivo genetic labeling, single cell genome-wide expression profiling, and classical birthdating to (i) identify specific molecular types of amacrine cells, (ii) demonstrate the molecular diversity of the amacrine cell class, and (iii) show that amacrine cell diversity arises at least in part through temporal patterning.
引用
收藏
页码:9495 / 9500
页数:6
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