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人非色素睫状上皮细胞分泌蛋白质组分析:视网膜神经节细胞系的分化因子表征

Protein profiling of human nonpigmented ciliary epithelium cell secretome: the differentiation factors characterization for retinal ganglion cell line.

作者信息

Yang Ming-Hui, Krishnamoorthy Raghu R, Jong Shiang-Bin, Chu Pei-Yu, Yang Yuan-Han, Chen Wen-Cheng, Chen Sharon Chia-Ju, Dibas Adnan, Chung Tze-Wen, Tyan Yu-Chang

机构信息

Department of Chemical and Material Engineering, National Yunlin University of Science and Technology, Douliou, Yunlin, Taiwan.

出版信息

J Biomed Biotechnol. 2011;2011:901329. doi: 10.1155/2011/901329. Epub 2011 Aug 10.

DOI:10.1155/2011/901329
PMID:21860587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3157028/
Abstract

The purpose of this paper was to characterize proteins secreted from the human nonpigmented ciliary epithelial (HNPE) cells, which have differentiated a rat retinal ganglion cell line, RGC-5. Undifferentiated RGC-5 cells have been shown to express several marker proteins characteristic of retinal ganglion cells. However, RGC-5 cells do not respond to N-methyl-D aspartate (NMDA), or glutamate. HNPE cells have been shown to secrete numbers of neuropeptides or neuroproteins also found in the aqueous humor, many of which have the ability to influence the activity of neuronal cells. This paper details the profile of HNPE cell-secreted proteins by proteomic approaches. The experimental results revealed the identification of 132 unique proteins from the HNPE cell-conditioned SF-medium. The biological functions of a portion of these identified proteins are involved in cell differentiation. We hypothesized that a differentiation system of HNPE cell-conditioned SF-medium with RGC-5 cells can induce a differentiated phenotype in RGC-5 cells, with functional characteristics that more closely resemble primary cultures of rat retinal ganglion cells. These proteins may replace harsh chemicals, which are currently used to induce cell differentiation.

摘要

本文的目的是对已分化出大鼠视网膜神经节细胞系RGC-5的人无色素睫状上皮(HNPE)细胞分泌的蛋白质进行表征。未分化的RGC-5细胞已被证明可表达几种视网膜神经节细胞特有的标记蛋白。然而,RGC-5细胞对N-甲基-D-天冬氨酸(NMDA)或谷氨酸无反应。HNPE细胞已被证明可分泌许多也存在于房水中的神经肽或神经蛋白,其中许多具有影响神经元细胞活性的能力。本文通过蛋白质组学方法详细介绍了HNPE细胞分泌蛋白的概况。实验结果显示,从HNPE细胞条件培养液SF-培养基中鉴定出132种独特的蛋白质。这些已鉴定蛋白质中的一部分的生物学功能与细胞分化有关。我们假设,HNPE细胞条件培养液SF-培养基与RGC-5细胞的分化系统可诱导RGC-5细胞出现分化表型,其功能特性更类似于大鼠视网膜神经节细胞的原代培养物。这些蛋白质可能会取代目前用于诱导细胞分化的刺激性化学物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3157028/65cb96bb7704/JBB2011-901329.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3157028/b8c563b5447c/JBB2011-901329.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3157028/77609f3ed3f1/JBB2011-901329.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3157028/65cb96bb7704/JBB2011-901329.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3157028/b8c563b5447c/JBB2011-901329.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3157028/77609f3ed3f1/JBB2011-901329.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3157028/65cb96bb7704/JBB2011-901329.003.jpg

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