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大鼠视网膜视杆双极细胞中蛋白激酶C样免疫反应性:一项发育研究。

Protein kinase C-like immunoreactivity in rod bipolar cells of the rat retina: a developmental study.

作者信息

Zhang D R, Yeh H H

机构信息

Department of Neurobiology and Anatomy, University of Rochester Medical Center, NY 14642.

出版信息

Vis Neurosci. 1991 May;6(5):429-37. doi: 10.1017/s0952523800001292.

DOI:10.1017/s0952523800001292
PMID:2069897
Abstract

In the retina of a variety of vertebrate species, a monoclonal antibody against protein kinase C (PKC) has been shown to label preferentially bipolar cells. Although the functional consequences of PKC activation in these cells is yet to be revealed, the present study was motivated in part by the possibility that the antibody might be used as a selective marker for examining the development of bipolar cells in the rat retina. Here, the developmental pattern and the dynamic changes of retinal cells expressing PKC-like immunoreactivity (PKC-LI) were studied and analyzed throughout postnatal life until adulthood. Upon its initial detection by immunohistochemistry on postnatal day (PD)-10, faint PKC-LI was limited to the central region of the retina, labeling cell bodies located at the scleral margin of the inner nuclear layer (INL) adjacent to the outer plexiform layer (OPL). On subsequent days, PKC-LI spread progressively to the peripheral retina and axon terminal bulbs at the vitreal margin of the inner plexiform layer (IPL) began showing the first signs of immunoreactive labeling. Not until PD-15, the time of eye opening, did PKC-LI in these cells increase to the extent such that their thin axons were immunoreactive. Each of these axons traversed the entire thickness of the IPL and divided into two or three short branches before ending as enlarged terminal bulbs. The morphology and the location of PKC-LI cells in both the developing and adult retina observed in our study are consistent with them being rod bipolar cells. By the end of the fourth postnatal week, the rod bipolar cells appeared mature, resembling those found in the adult.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在多种脊椎动物的视网膜中,一种针对蛋白激酶C(PKC)的单克隆抗体已被证明能优先标记双极细胞。尽管PKC在这些细胞中激活的功能后果尚未揭示,但本研究部分是受该抗体可能用作检查大鼠视网膜双极细胞发育的选择性标记物这一可能性的推动。在此,研究并分析了整个出生后直至成年期表达PKC样免疫反应性(PKC-LI)的视网膜细胞的发育模式和动态变化。在出生后第10天(PD-10)通过免疫组织化学首次检测到时,微弱的PKC-LI局限于视网膜的中央区域,标记位于内核层(INL)与外网状层(OPL)相邻的巩膜边缘的细胞体。在随后的几天里,PKC-LI逐渐扩散到周边视网膜,并且在内网状层(IPL)玻璃体边缘的轴突终末球开始显示出免疫反应性标记的最初迹象。直到睁眼的PD-15,这些细胞中的PKC-LI才增加到其细轴突具有免疫反应性的程度。这些轴突中的每一个都穿过IPL的整个厚度,并在作为扩大的终末球结束之前分成两三个短分支。在我们的研究中观察到的发育中和成年视网膜中PKC-LI细胞的形态和位置与它们是视杆双极细胞一致。到出生后第四周结束时,视杆双极细胞看起来已经成熟,类似于成年动物中的细胞。(摘要截短于250字)

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