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SSEA4 是一种潜在的人眼角膜上皮干/祖细胞富集的阴性标志物。

SSEA4 is a potential negative marker for the enrichment of human corneal epithelial stem/progenitor cells.

机构信息

Cornea and Uveitis Division, Jules Stein Eye Institute, University of California, Los Angeles, California 90095, USA.

出版信息

Invest Ophthalmol Vis Sci. 2011 Aug 11;52(9):6315-20. doi: 10.1167/iovs.11-7518.

Abstract

PURPOSE

To examine the expression of stage-specific embryonic antigen-4 (SSEA4) in the epithelium of the human ocular surface and characterize SSEA4(+) and SSEA4(-) limbal epithelial cells.

METHODS

SSEA4 expression in the human cornea and limbus was examined by RT-PCR and immunohistochemistry. SSEA4(+) and SSEA4(-) cells were then separated by using magnetic beads. The phenotypes of these two cell populations were evaluated on the basis of cell size, clonogenic assay, and expression of putative limbal stem cell (LSC) and corneal epithelial differentiation markers.

RESULTS

SSEA4 was expressed in all layers of the corneal and anterior limbal epithelia. Discrete clusters of SSEA4(+) cells were present in the central and posterior limbal epithelia. SSEA4(+) cells accounted for an average of 40% of the total limbal epithelial cells. The SSEA4(-) population contained five times more small cells (≤11 μm in diameter) than did the SSEA4(+) population. The expression levels of the putative LSC markers ABCG2, ΔNp63α, and cytokeratin (K)14 were significantly higher in the SSEA4(-) population than in the SSEA4(+) population. The SSEA4(-) cells also expressed a significantly higher level of N-cadherin, but a lower level of the differentiation marker K12. The colony-forming efficiency in the SSEA4(-) population was 25.2% (P = 0.04) and 1.6-fold (P < 0.05) higher than in the unsorted population and the SSEA4(+) population, respectively.

CONCLUSIONS

SSEA4 is highly expressed in differentiated corneal epithelial cells, and SSEA4(-) limbal epithelial cells contain a higher proportion of limbal stem/progenitor cells. SSEA4 could be used as a negative marker to enrich the isolation of LSCs.

摘要

目的

检测人眼表面上皮组织中阶段特异性胚胎抗原-4(SSEA4)的表达,并对 SSEA4(+)和 SSEA4(-) 角膜缘上皮细胞进行特征分析。

方法

通过 RT-PCR 和免疫组织化学检测 SSEA4 在人眼角膜和角膜缘中的表达。然后,使用磁珠分离 SSEA4(+)和 SSEA4(-)细胞。根据细胞大小、克隆形成实验以及假定的角膜缘干细胞(LSC)和角膜上皮分化标志物的表达,评估这两种细胞群体的表型。

结果

SSEA4 在角膜和前角膜缘上皮的所有层中均有表达。在中央和后角膜缘上皮中存在离散的 SSEA4(+)细胞簇。SSEA4(+)细胞占角膜缘上皮细胞总数的平均 40%。SSEA4(-)群体中的小细胞(直径≤11μm)数量是 SSEA4(+)群体的五倍多。SSEA4(-)群体中假定的 LSC 标志物 ABCG2、ΔNp63α 和细胞角蛋白(K)14 的表达水平明显高于 SSEA4(+)群体。SSEA4(-)细胞还表达了更高水平的 N-钙黏蛋白,但分化标志物 K12 的表达水平较低。SSEA4(-)细胞群体的集落形成效率分别比未分选群体和 SSEA4(+)群体高 25.2%(P=0.04)和 1.6 倍(P<0.05)。

结论

SSEA4 在分化的角膜上皮细胞中高度表达,SSEA4(-) 角膜缘上皮细胞中包含更高比例的角膜缘干细胞/祖细胞。SSEA4 可作为一种负性标记物,用于富集分离 LSCs。

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