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

机译:角蛋白12 mRNA表达可以作为爆腹外植体培养的早期角膜标记物

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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. Electronic supplementary material The online version of this article (10.1007/s10616-020-00373-z) contains supplementary material, which is available to authorized users.
机译:这种调查旨在通过爆腹外植体培养物的转录分析确定早期的角膜标记和结膜上皮分化,并研究了已知的角膜和结膜分化标志物的早期分化模式。 2?mm的旧版区域的冲击活组织检查是从狮子角膜银行的6个捐助者获得Saar-Lorloux / Trier-Westpfalz。将肢体外植体解剖到角膜和结膜活检部分。将活组织检查置于上皮面下降到12个孔中。一旦外交细胞达到汇合,就被收获了。通过QPCR测量角膜分化标志物KRT12,KRT3,DSG1,PAX6,ADH7和ALDH1A1,结膜标记KRT19,KRT13和干细胞标记物ABCG2的mRNA表达。使用Western印迹评估KRT12和PAX6蛋白表达。结果表明,来自活组织检查的角膜侧的kRT12 mRNA表达显着较高,如来自结膜侧的那些(p?= 0.0043)。与来自二肢活检(P≥1013)的逾越节细胞的标记表达相比,其他分析的标记的MRNA表达没有显着差异(p?&β0.13)。 KRT12和PAX6 Western印迹分析显示出从两侧收获的细胞没有差异。总之,KRT12 mRNA可能是标记物,以测量来自尾骨活检的细胞的角膜原点,未知的角膜和结膜祖细胞组成。 KRT3,DSG1,PAX6,ADH7,ALDH1A1,KRT19,KRT13和ABCG2 mRNA以及KRT12和PAX6蛋白表达不能有助于区分角膜与缘活组织检查的结膜细胞同一性。电子补充材料本文的在线版本(10.1007 / s10616-020-00373-z)包含辅助材料,可供授权用户使用。

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