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角蛋白12信使核糖核酸的表达可作为角膜缘外植体培养的早期角膜标志物。

Keratin 12 mRNA expression could serve as an early corneal marker for limbal explant cultures.

作者信息

Shi Lei, Stachon Tanja, Käsmann-Kellner Barbara, Seitz Berthold, Szentmáry Nóra, Latta Lorenz

机构信息

Department of Ophthalmology, Saarland University Medical Center, Kirrberger Str. 100, 66424, Homburg, Saar, Germany.

The First Affiliated Hospital of USTC, Division of Life Science and Medicine, University of Science and Technology of China, Hefei, Anhui, People's Republic of China.

出版信息

Cytotechnology. 2020 Apr;72(2):239-245. doi: 10.1007/s10616-020-00373-z. Epub 2020 Feb 3.

Abstract

This investigation aimed to identify early corneal marker and conjunctival epithelial differentiation through transcriptional analysis of limbal explant cultures and study early differentiation patterns of known corneal and conjunctival differentiation markers. 2 mm punch biopsies of limbal region were obtained from 6 donors of the Lions Cornea Bank Saar-Lorloux/Trier-Westpfalz. Limbal explants were dissected into corneal and conjunctival biopsy sections. Biopsies were placed with epithelial side down into 12 Wells. As soon as the outgrowing cells had reached confluence, they were harvested. mRNA expression of corneal differentiation markers KRT12, KRT3, DSG1, PAX6, ADH7 and ALDH1A1, conjunctival markers KRT19, KRT13 and stem cell marker ABCG2 were measured via qPCR. KRT12 and PAX6 protein expressions were evaluated using Western Blot. Results suggested that KRT12 mRNA expression was significantly higher in outgrowing cells from the corneal side of the biopsies as in those from the conjunctival side (p = 0.0043). There was no significant difference in mRNA expression of other analyzed markers comparing with marker expression of outgrown cells from both limbal biopsies (p > 0.13). KRT12 and PAX6 Western Blot analysis showed no difference in cells harvested from both sides. In conclusion, KRT12 mRNA might be a marker to measure corneal origin of cells from limbal biopsies with unknown composition of corneal and conjunctival progenitor cells. KRT3, DSG1, PAX6, ADH7, ALDH1A1, KRT19, KRT13 and ABCG2 mRNA as well as KRT12 and PAX6 protein expression could not contribute to differentiate corneal from conjunctival cell identity from limbal biopsies.

摘要

本研究旨在通过对角膜缘外植体培养物进行转录分析,确定早期角膜标志物和结膜上皮分化情况,并研究已知角膜和结膜分化标志物的早期分化模式。从萨尔 - 洛尔洛克斯/特里尔 - 韦斯特普法尔茨狮子角膜库的6名供体获取角膜缘区域2毫米的穿刺活检组织。将角膜缘外植体解剖为角膜和结膜活检切片。将活检组织上皮面朝下放置在12孔板中。一旦生长出的细胞达到汇合状态,就将其收获。通过qPCR测量角膜分化标志物KRT12、KRT3、DSG1、PAX6、ADH7和ALDH1A1、结膜标志物KRT19、KRT13以及干细胞标志物ABCG2的mRNA表达。使用蛋白质印迹法评估KRT12和PAX6蛋白表达。结果表明,活检组织角膜侧生长出的细胞中KRT12 mRNA表达显著高于结膜侧(p = 0.0043)。与来自两个角膜缘活检组织生长出的细胞的标志物表达相比,其他分析标志物的mRNA表达没有显著差异(p > 0.13)。KRT12和PAX6蛋白质印迹分析显示,从两侧收获的细胞没有差异。总之,KRT12 mRNA可能是一种标志物,用于测量来自角膜和结膜祖细胞组成未知的角膜缘活检组织中细胞的角膜来源。KRT3、DSG1、PAX6、ADH7、ALDH1A1、KRT19、KRT13和ABCG2 mRNA以及KRT12和PAX6蛋白表达无法区分角膜缘活检组织中的角膜细胞和结膜细胞身份。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9926/7192984/424d8e9f6304/10616_2020_373_Fig1_HTML.jpg

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