Xrx1 controls proliferation and multipotency of retinal progenitors

被引:55
作者
Casarosa, S
Amato, MA
Andreazzoli, M
Gestri, G
Barsacchi, G
Cremisi, F
机构
[1] Univ Pisa, Sez Biol Cellulare & Sviluppo, Dipartimento Fisiol & Biochim, I-56010 Pisa, Italy
[2] Univ Pisa, Ctr Eccellenza AmbiSEN, Pisa, Italy
[3] Scuola Normale Super Pisa, I-56100 Pisa, Italy
关键词
D O I
10.1016/S1044-7431(02)00025-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We investigated the function of Xrx1 during Xenopus retinogenesis. Xrx1 overexpression lengthens mitotic activity and ectopically activates the expression of markers of undifferentiated progenitors in the developing retina. We assayed Xrx1 ability to support proliferation with a cell-autonomous mechanism by in vivo lipofection of single retinal progenitors. Xrx1 overexpression increases clonal proliferation while Xrx1 functional inactivation exerts the opposite effect. We also compared the effects of Xrx1 with those of the cyclin-dependent kinase cdk2, a strong mitotic promoter. Despite the similar increase in clonal proliferation displayed by both factors, Xrx1 and cdk2 act differently on retinal cell fate determination. cdk2/cyclinA2 lipofected retinas show a decrease in early-born cell types as ganglion cells and cones and an increase in late-born types such as bipolar neurons. On the contrary, Xrx1 lipofected retinas show no changes in the proportions of the different cell types, thus suggesting a role in supporting multipotency of retinal progenitors. (C) 2003 Elsevier Science (USA). All rights reserved.
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页码:25 / 36
页数:12
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