MEK-ERK signaling in adult newt retinal pigment epithelium cells is strengthened immediately after surgical induction of retinal regeneration

被引:19
|
作者
Mizuno, Aki [2 ]
Yasumuro, Hirofumi [2 ]
Yoshikawa, Taro [2 ]
Inami, Wataru [2 ]
Chiba, Chikafumi [1 ]
机构
[1] Univ Tsukuba, Fac Life & Environm Sci, Tsukuba, Ibaraki 3058572, Japan
[2] Univ Tsukuba, Grad Sch Life & Environm Sci, Tsukuba, Ibaraki 3058572, Japan
关键词
Retina; Regeneration; Newt; MEK; ERK; Retinal pigment epithelium; STEM-CELLS; TRANSDIFFERENTIATION; RPE; PROLIFERATION; PATHWAYS;
D O I
10.1016/j.neulet.2012.06.037
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Adult newt retinal pigment epithelium (RPE) cells are mitotically quiescent in the physiological condition, but upon a traumatic injury of the neural retina (NR) they re-enter the cell-cycle and eventually regenerate the missing NR. Here, to understand the mechanism underlying the cell-cycle re-entry of RPE cells following NR injury, we first investigated changes in MEK-ERK signaling activity in RPE cells upon removal of the NR (retinectomy) from the eye of living animals, and found that ERK-mediated signaling activity is elevated quickly (in 30 min) upon retinectomy. In addition, we found, in in vitro analyses, that immediate early activation of MEK-ERK signaling may occur in RPE cells upon NR injury, intensifying the MEK-ERK signaling itself through up-regulation of the expression of constituent molecules in the pathway, and that 1-h blockade of such early MEK-ERK signaling interferes with the cell-cycle re-entry, which occurs 5-10 days later. Together, these results provide us with insight that elevation of MEK-ERK signaling activity upon NR injury may be a key process for mitotically quiescent RPE cells to re-enter the cell-cycle, leading to retinal regeneration. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:39 / 44
页数:6
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