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从成人外周视网膜分离出的增殖细胞在诱导分化时仅短暂上调关键视网膜标志物。

Proliferative Cells Isolated from the Adult Human Peripheral Retina only Transiently Upregulate Key Retinal Markers upon Induced Differentiation.

作者信息

Johnsen Erik O, Frøen Rebecca C, Olstad Ole Kristoffer, Nicolaissen Bjørn, Petrovski Goran, Moe Morten C, Noer Agate

机构信息

a Center for Eye Research, Department of Ophthalmology , Oslo University Hospital and University of Oslo , Oslo , Norway.

b Norwegian Center for Stem Cell Research , Oslo University Hospital and University of Oslo , Oslo , Norway.

出版信息

Curr Eye Res. 2018 Mar;43(3):340-349. doi: 10.1080/02713683.2017.1403630. Epub 2017 Nov 21.

Abstract

UNLABELLED

Purpose/Aim: The adult human retina has limited regenerative potential, and severe injury will result in permanent damage. Lower vertebrates handle retinal injury by activating neural stem cells (NSCs) in the ciliary marginal zone (CMZ). Müller glia-like cells expressing markers of NSCs are also present in the peripheral retina (PR) of the adult human eye, leading to the hypothesis that a CMZ-like zone might exists also in humans. In order to shed further light on this hypothesis we investigated the in vitro differentiation potential of proliferative cells isolated from the adult human PR towards a retinal phenotype.

MATERIALS AND METHODS

Proliferative cells were isolated from the peripheral retina of human eyes (n = 6) within 24 to 48 hours post mortem and further expanded for 2 or 3 passages before being differentiated for 1-3 weeks. Gene expression was analyzed by microarray and qRT-PCR analysis, while protein expression was identified by immunocytochemistry.

RESULTS

A high density of cells co-staining with markers for progenitor cells and Müller glia was found in situ in the PR. Cells isolated from this region and cultured adherently showed fibrillary processes and were positive for the immature marker Nestin and the glial marker GFAP, while a few co-expressed PAX6. After 7 days of differentiation, there was a transient upregulation of early and mature photoreceptor markers, including NRL, CRX, RHO and RCVRN, as well as the Müller cell and retinal pigmented epithelium (RPE) marker CRALBP, and the early RPE marker MITF. However, the expression of all these markers dropped from Day 14 and onwards.

CONCLUSIONS

Upon exposure of proliferating cells from the adult human PR to differentiating conditions in culture, there is a widespread change in morphology and gene expression, including the upregulation of key retinal markers. However, this upregulation is only transient and decreases after 14 days of differentiation.

摘要

未标注

目的/目标:成年人类视网膜的再生潜力有限,严重损伤会导致永久性损害。低等脊椎动物通过激活睫状边缘区(CMZ)的神经干细胞(NSC)来应对视网膜损伤。在成年人类眼睛的周边视网膜(PR)中也存在表达NSC标志物的穆勒胶质样细胞,这引发了一种假说,即人类可能也存在类似CMZ的区域。为了进一步阐明这一假说,我们研究了从成年人类PR分离的增殖细胞向视网膜表型的体外分化潜力。

材料与方法

在死后24至48小时内从人眼(n = 6)的周边视网膜分离增殖细胞,并在进一步传代培养2或3代后进行1至3周的分化。通过微阵列和qRT-PCR分析来分析基因表达,同时通过免疫细胞化学鉴定蛋白质表达。

结果

在PR中原位发现了高密度的与祖细胞和穆勒胶质细胞标志物共染色的细胞。从该区域分离并贴壁培养的细胞显示出纤维状突起,对未成熟标志物巢蛋白和胶质标志物胶质纤维酸性蛋白呈阳性,而少数细胞共表达PAX6。分化7天后,早期和成熟光感受器标志物,包括神经视网膜亮氨酸拉链蛋白(NRL)、锥-杆细胞同源框蛋白(CRX)、视紫红质(RHO)和视锥细胞视黄醛结合蛋白(RCVRN),以及穆勒细胞和视网膜色素上皮(RPE)标志物视网膜色素上皮特异性蛋白(CRALBP)和早期RPE标志物小眼畸形相关转录因子(MITF)出现短暂上调。然而,所有这些标志物的表达从第14天及以后开始下降。

结论

将成年人类PR中的增殖细胞置于培养中的分化条件下时,其形态和基因表达会发生广泛变化,包括关键视网膜标志物的上调。然而,这种上调只是短暂的,在分化14天后会下降。

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