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Ephrin-A2 and -A3 are negative regulators of the regenerative potential of Müller cells
引用本文:Zhu Ruilin,Cho Kin-Sang,Chen Dong Feng,Yang Liu. Ephrin-A2 and -A3 are negative regulators of the regenerative potential of Müller cells[J]. 中华医学杂志(英文版), 2014, 127(19): 3438-3442
作者姓名:Zhu Ruilin  Cho Kin-Sang  Chen Dong Feng  Yang Liu
基金项目:grants from the Department of Veterans Affairs (1I01RX000110), the Department of Defense (W81XWH-09-2-0091), Lion’s Foundation Grants to D.F.C. and K.S.C. and the National Natural Science Foundation of China (No. 81170837).
摘    要:
Background In a previous study, we demonstrated that ephrin-A2 and -A3 negatively regulate the growth of neural progenitor cells in the central nervous system. Adult mice deficient in ephrin-A2 and -A3 (A2+A3+) displayed active ongoing neurogenesis throughout the brain, and mice deficient in ephrin-A3 alone showed increased proliferation of ciliary epithelium derived retinal stem cells. This study aimed to detect that the increase in proliferation and neurogenic potential of MOiler cells is influenced by the absence of ephrin-A2 and -A3. Methods We assessed the retinal and MOiler cell expression of ephrin-As and their receptor and neural progenitor cell markers by immunostaining and real-time PCR. We cultured purified primary MOiler cells derived from wild-type and A2+A3+ mice in a defined culture medium that enables trans-differentiation of Mu11er cells into retinal neurons. To evaluate proliferating MOiler cells in vivo, we injected 5'-ethylnyl-2-deoxiuridine (EdU) intraperitoneally to adult mice. Results Expression of ephrin-A2/A3 and their receptor EphA4 were detected in the retinas of adult mice, with EphA4 expression particularly enriched in MOiler cells. MOiler cells of A2+A3+ mice exhibited significantly elevated expression of retinal progenitor cell markers, Pax6 and Chx10, when compared with those from wild-type mice. Moreover, a higher percentage of Mu11er cells of A2+A3+ mice trans-differentiated and became recoverin+ and β-Ⅲ-tublin+ in the culture than those from wild type mice. Strikingly, an increased number of EdU+ retinal cells was detected in the retinas of adult A2+A3+ mice as compared with wild-type mice. Conclusions Ephrin-A2 and -A3 are negative regulators of the proliferative and neurogenic potentials of Mu11er cells. Manipulating ephrin-A signaling may thus represent a novel strategy for stimulating neuroregeneration from endogenous progenitors to participate in retinal repair in case of disease or damage.

关 键 词:祖细胞  神经再生  负调控  中枢神经系统  成年小鼠  细胞增殖  微管蛋白  视网膜

Ephrin-A2 and-A3 are negative regulators of the regenerative potential of Muller cells
Zhu Ruilin,Cho Kin-Sang,Chen Dong Feng and Yang Liu. Ephrin-A2 and-A3 are negative regulators of the regenerative potential of Muller cells[J]. Chinese medical journal, 2014, 127(19): 3438-3442
Authors:Zhu Ruilin  Cho Kin-Sang  Chen Dong Feng  Yang Liu
Affiliation:[1]Department of Ophthalmology, Peking University First Hospital; KeyLaboratory of Vision Loss and Restoration, Ministry of Education,Beijing, China; [2]Schepens Eye Research Institute, Massachusetts Eye and Ear,Harvard Medical School, Boston, MA, USA
Abstract:
Muller cell stem cell retinal regeneration
Keywords:Muller cell  stem cell  retinal regeneration
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