小鼠视网膜片层化及神经干细胞的增殖与分化

孔维芳 周洁 金海啸 薛帅 邓锦波

解剖学报 ›› 2013, Vol. 44 ›› Issue (1) : 13-18.

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解剖学报 ›› 2013, Vol. 44 ›› Issue (1) : 13-18. DOI: 10.3969/j.issn.0529-1356.2013.01.003
神经生物学

小鼠视网膜片层化及神经干细胞的增殖与分化

  • 孔维芳,周洁,金海啸,薛帅,邓锦波*
作者信息 +

Lamination of mouse retina and the neural stem cell proliferation and differentiation

  • KONG Wei-fang,ZHOU Jie,JIN Hai-xiao,XUE Shuai,DENG Jin-bo*
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摘要

目的 通过观察小鼠视网膜神经干细胞增殖与双极细胞分化过程,研究视网膜的发生及片层化。方法 应用免疫荧光、5’-溴脱氧尿嘧啶核苷(BrdU)检测技术和HE染色法对胚胎及出生后小鼠视网膜形态结构及神经干细胞的增殖、分化进行观察,对视网膜BrdU和蛋白激酶Cα(PKC-α)阳性细胞密度进行统计。结果 1.小鼠视网膜在胚胎时期分化出色素上皮层、神经母细胞层和神经节细胞层。出生后,神经母细胞层逐渐分化出各个层,至小鼠睁眼时基本分化完全。2.小鼠视网膜干细胞在胚胎期大量增殖,出生后增殖放慢并逐渐分化为各类细胞。经统计分析发现,视网膜干细胞在胚胎时期数量逐渐增多,到出生当天数量达到最大值,出生后,神经干细胞开始分化,数量逐渐减少。3.小鼠视网膜双极细胞从出生后第5天(P5)开始发育,至P20时发育完全。结论 小鼠视网膜的片层化与其功能的成熟相一致,视网膜的神经干细胞在出生后前期为分化高峰期,逐渐分化为不同类型的细胞。P10以后仅在睫状体处存在神经干细胞,可能与成年以后的修复功能相关。

Abstract

Objective To investigate the retina neural stem cell proliferation and the differentiatiation of bipolar cells, the histogenesis and lamination of mouse retina. Methods The immunofluorescent labeling, BrdU detection and HE staining were carried out in the study. BrdU and PKC-α positive cells from embryonic and postnatal retina were measured, and the regression analyses and statistical tests were performed. Results 1. In the early embryonic days, the pigment epithelium, neuroblastoma layer were visualized. After birth, neuroblastoma layer gradually developed into different layers of retina, and the fully developed retina was observed at the age of eye opening. 2. The stem cells in the retina proliferated and differentiated into various types of cells during the embryonic days, and the
proliferation slowed down after birth. With statistical analysis, we found that the number of retinal stem cells gradually increased during the embryonic period and reached the peak at P0. After birth, the neural stem cell started to differentiate, therefore their number reduced gradually. 3. Mouse retinal bipolar cells appeared at P5, and they did not mature until P20. Conclusion The neuroblastoma layer plays an important role in the lamination of retina, and the maturity of retinal morphology is consistent with its functions. The neural stem cell proliferation and differentiation reach their peaks at the neonate day, and the stem cells gradually differentiate into different cell types. In the adult, there are neural stem cells only in the ciliary body, suggesting their repair function after birth.

关键词

双极细胞 / 分化 / 神经干细胞 / 增殖 / 视网膜 / 免疫荧光 / 小鼠

Key words

Bipolar cells / Differentiation / Neural stem cells / Proliferation / Retina / Immunofluorescence / Mouse

引用本文

导出引用
孔维芳 周洁 金海啸 薛帅 邓锦波. 小鼠视网膜片层化及神经干细胞的增殖与分化[J]. 解剖学报. 2013, 44(1): 13-18 https://doi.org/10.3969/j.issn.0529-1356.2013.01.003
KONG Wei-fang,ZHOU Jie,JIN Hai-xiao,XUE Shuai,DENG Jin-bo. Lamination of mouse retina and the neural stem cell proliferation and differentiation[J]. Acta Anatomica Sinica. 2013, 44(1): 13-18 https://doi.org/10.3969/j.issn.0529-1356.2013.01.003

参考文献

 

1] Peng Q, Liu ShY, Ren PX. A histological observation on the retinas from neonatal mice of different day-ages[J].Chinese Journal of Ocular Fundus Diseaes,1999,15(3):174-176.(in Chinese)
彭清,刘舒娅,任佩贤.不同日龄新生小鼠视网膜组织学观察[J]. 中华眼底病杂志,1999,15(3):174-176.
2] Cai ZhM, Chen RH, Chen XM. The light and electron microscopy observation of the retina in human fetus[J].Chinese Journal of Anatomy, 1991,14(3):212-215.(in Chinese)
蔡兆明,陈瑞华,陈小铭. 人胎视网膜发生的光镜和电镜观察[J]. 解剖学杂志,1991,14(3):212-215.
3]Le RD, Rayner K, Rex M, et al. The transcription factor cSox2 and neuropeptide Y define a novel subgroup of amacrine cells in the retina[J]. J Anat, 2002,200(1):51-56. 
4] Yin YY, Hua Q. Retinal mosaics related to eye development and formation[J]. Progress in Biochemistry and Biophysics, 2001,28(2):137-39.(in Chinese)
殷咏仪,华茜. 视网膜发育与形成的“镶嵌模型”[J]. 生物化学与生物物理进展,2001,28(2):137-139.
5]Liang SY, Lee GA, Shields D. Self-tonometry in glaucoma management——past,present and future[J]. Surv Ophthalmol, 2009,54(4):450-462.
6]Avilion AA, Nicolis SK, Pevny LH, et al. Multipotent cell lineages in early mouse development depend on Sox2 function[J]. Genes Dev, 2003, 17(1):126-140.
7]Moriarty P,Dickson AJ,Erichsen JT,et al. Protein kinase C isoenzyme expression in retinal cells[J].Ophthalmic Res,2000,32(2-3):57-60.
8] Huang XY, Yin ZhQ, Wang ShJ, et al. Distribution of stem cells of optic cup in rat embryos[J]. Acta Academiae Medicinae Mlitaris Tertiae, 2005,27(6):504-506.(in Chinese)
黄小勇,阴正勤,王仕军,等.大鼠胚胎视杯视网膜干细胞的分布研究[J].第三军医大学学报,2005,27(6):504-506.
9]Sun X, Jiang R, Zhang Y, et al. Gene expression and differentiation characteristics in mice E13.5 and E17.5 neural retinal progenitors[J]. Mol Vis, 2009, 2(15):2503-2514.
10]Suzuki S, KaneKo A. Identification of bipolar cell subtypes by protein kinase c-like immunoreactivity in the goldfish retina[J]. Vis Neurosci,1990,5(3):223-230.[11]Meyer JS, Katz ML, Maruniak JA, et al. Embryonic stem cell-derived neural progenitors incorporate into degenerating retina and enhance survival of host photoreceptors[J]. Stem Cells, 2006,24(2):274-283. 
12]Agathocleous M, Iordanova I, Willardsen MI, et al. A directional Wnt/beta-catenin-Sox2-proneural pathway regulates the transition from proliferation to differentiation in the Xenopus retina[J].Development, 2009, 136(19):3289-3299.
13]Domyan ET, Ferretti E, Throckmorton K, et al. Signaling through BMP receptors promotes respiratory identity in the foregut via repression of Sox2[J]. Development, 2011, 138(5):971-981.
14]Cavallaro M, Mariani J, Lancini C, et al. Impaired generation of mature neurons by neural stem cells from hypomorphic Sox2 mutants[J]. Development, 2008, 135(3):541-557. 
15]Ferri AL, Cavallaro M, Braida D, et al. Sox2 deficiency causes neurodegeneration and impaired neurogenesis in the adult mouse brain[J].Development, 2004, 131(15):3805-3819.
16]Lin YP, Ouchi Y, Satoh S, et al. Sox2 plays a role in the induction of amacrine and Müller glial cells in mouse retinal progenitor cells[J]. Invest Ophthalmol Vis Sci, 2009, 50(1):68-74.
17]Taranova OV, Magness ST, Fagan BM, et al. SOX2 is a dose-dependent regulator of retinal neural progenitor competence[J]. Genes Dev, 2006, 20(9):1187-1202.[18]Jeon CJ, Strettoi E, Masland RH. The major cell populations of the mouse retina[J]. Neurosci, 1998,18(21):8936-8946.
19]Wässle H, Puller C, Müller F, et al. Cone contacts, mosaics, and territories of bipolar cells in the mouse retina[J]. Neurosci, 2009, 29(1):106-117. 

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国家自然科学基金资助项目


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