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Multipotent retinal progenitors express developmental markers, differentiate into retinal neurons, and preserve light-mediated behavior
被引:251
作者:
Klassen, HJ
Ng, TF
Kurimoto, Y
Kirov, I
Shatos, M
Coffey, P
Young, MJ
机构:
[1] Harvard Univ, Sch Med, Dept Ophthalmol, Schepens Eye Res Inst, Boston, MA 02114 USA
[2] Univ Sheffield, Dept Psychol, Visual Transplantat Res Grp, Sheffield S10 2TN, S Yorkshire, England
[3] Childrens Hosp Orange Cty, CHOC Res Inst, Orange, CA 92668 USA
基金:
英国医学研究理事会;
关键词:
D O I:
10.1167/iovs.04-0511
中图分类号:
R77 [眼科学];
学科分类号:
100212 ;
摘要:
Purpose. To use progenitor cells isolated from the neural retina for transplantation studies in mice with retinal degeneration. Methods. Retinal progenitor cells from postnatal day 1 green fluorescent protein-transgenic mice were isolated and characterized. These cells can be expanded greatly in culture and express markers characteristic of neural progenitor cells and/or retinal development. Results. After they were grafted to the degenerating retina of mature mice, a subset of the retinal progenitor cells developed into mature neurons, including presumptive photoreceptors expressing recoverin, rhodopsin, or cone opsin. In rho(-/-) hosts, there was rescue of cells in the outer nuclear layer (ONL), along with widespread integration of donor cells into the inner retina, and recipient mice showed improved light-mediated behavior compared with control animals. Conclusions. These findings have implications for the treatment of retinal degeneration, in which neuronal replacement and photoreceptor rescue are major therapeutic goals.
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页码:4167 / 4173
页数:7
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