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转录因子Nr2e3在视网膜祖细胞中发挥作用,抑制视锥细胞的生成。

The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation.

作者信息

Haider Neena B, Demarco Paul, Nystuen Arne M, Huang Xiaona, Smith Richard S, McCall Maureen A, Naggert Jürgen K, Nishina Patsy M

机构信息

Department of Genetics, University of Nebraska Medical Center, Omaha, Nebraska 68198, USA.

出版信息

Vis Neurosci. 2006 Nov-Dec;23(6):917-29. doi: 10.1017/S095252380623027X.

Abstract

The transcription factor Nr2e3 is an essential component for development and specification of rod and cone photoreceptors; however, the mechanism through which it acts is not well understood. In this study, we use Nr2e3(rd7/rd7) mice that harbor a mutation in Nr2e3, to serve as a model for the human retinal disease Enhanced S Cone Syndrome. Our studies reveal that NR2E3 is expressed in late retinal progenitors and differentiating photoreceptors of the developing retina and localized to the cell bodies of mature rods and cones. In particular, we demonstrate that the abnormal increase in cone photoreceptors observed in Nr2e3(rd7/rd7) mice arise from ectopic mitotic progenitor cells that are present in the outer nuclear layer of the mature Nr2e3(rd7/rd7) retina. A prolonged phase of proliferation is observed followed by abnormal retinal lamination with fragmented and disorganized photoreceptor synapses that result in a progressive loss of rod and cone function. An extended and pronounced wave of apoptosis is also detected at P30 and temporally correlates with the phase of prolonged proliferation. Approximately twice as many apoptotic cells were detected compared to proliferating cells. This wave of apoptosis appears to affect both rod and cone cells and thus may account for the concurrent loss of rod and cone function. We further show that Nr2e3(rd7/rd7) cones do not express rod specific genes and Nr2e3(rd7/rd7) rods do not express cone specific genes. Our studies suggest that, based on its temporal and spatial expression, NR2E3 acts simultaneously in different cell types: in late mitotic progenitors, newly differentiating post mitotic cells, and mature rods and cones. In particular, this study reveals the function of NR2E3 in mitotic progenitors is to repress the cone generation program. NR2E3 is thus one of the few genes known to influence the competency of retinal progenitors while simultaneously directing the rod and cone differentiation.

摘要

转录因子Nr2e3是视杆和视锥光感受器发育及分化的重要组成部分;然而,其作用机制尚未完全明确。在本研究中,我们使用携带Nr2e3突变的Nr2e3(rd7/rd7)小鼠作为人类视网膜疾病增强型S视锥综合征的模型。我们的研究表明,NR2E3在发育中视网膜的晚期视网膜祖细胞和分化中的光感受器中表达,并定位于成熟视杆和视锥的细胞体。特别是,我们证明在Nr2e3(rd7/rd7)小鼠中观察到的视锥光感受器异常增加源于成熟Nr2e3(rd7/rd7)视网膜外核层中存在的异位有丝分裂祖细胞。观察到增殖期延长,随后出现视网膜分层异常,光感受器突触碎片化和紊乱,导致视杆和视锥功能逐渐丧失。在P30时还检测到延长且明显的凋亡波,并且在时间上与延长的增殖期相关。检测到的凋亡细胞数量约为增殖细胞的两倍。这一波凋亡似乎影响视杆和视锥细胞,因此可能解释了视杆和视锥功能的同时丧失。我们进一步表明,Nr2e3(rd7/rd7)视锥细胞不表达视杆特异性基因,Nr2e3(rd7/rd7)视杆细胞不表达视锥特异性基因。我们的研究表明,基于其时间和空间表达,NR2E3在不同细胞类型中同时发挥作用:在晚期有丝分裂祖细胞、新分化的有丝分裂后细胞以及成熟的视杆和视锥细胞中。特别是,本研究揭示了NR2E3在有丝分裂祖细胞中的功能是抑制视锥细胞生成程序。因此,NR2E3是已知的少数几个既能影响视网膜祖细胞的能力,又能同时指导视杆和视锥细胞分化的基因之一。

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