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人角质形成细胞系SV-K14中角化包膜前体蛋白的鉴定及其亚细胞分布

Identification and subcellular distribution of cornified envelope precursor proteins in the transformed human keratinocyte line SV-K14.

作者信息

Michel S, Schmidt R, Robinson S M, Shroot B, Reichert U

出版信息

J Invest Dermatol. 1987 Mar;88(3):301-5. doi: 10.1111/1523-1747.ep12466177.

Abstract

SV-40 transformed human foreskin keratinocytes (line SV-K14) develop under conditions of serum starvation the competence to form cornified envelopes that are characteristic of terminally differentiating epidermal cells. In this cell line, the final assembly of the envelope does not occur spontaneously but must be induced using a calcium ionophore. Five potential precursor proteins with molecular weights of 140K, 90K, 61K, 53K, and 36K, respectively, could be detected in the extracts of envelope competent and noncompetent cells. The 61 kD and the 36 kD precursors were specifically decorated in immunoblots when using an antiserum directed against the purified cornified envelope of SV-K14 cells. The 140 kD protein was identified as involucrin by means of a commercial anti-involucrin antibody. Part of the 61 kD protein was found to be inserted into the plasma membrane after the cells gained envelope competence. The set of precursor proteins used by SV-K14 cells differed markedly from those described in the literature for epidermal cells in vivo and for normal human keratinocytes in vitro. Furthermore, cyanogen bromide cleavage of purified envelopes from transformed and normal keratinocytes revealed a completely different peptide pattern. This indicates that the exact molecular composition of the cornified envelope may not be strictly determined and may vary according to the availability of potential substrate proteins at the very moment when the cross-linking enzyme, the plasma membrane associated transglutaminase, becomes functional.

摘要

SV - 40转化的人包皮角质形成细胞(SV - K14细胞系)在血清饥饿条件下会形成具有终末分化表皮细胞特征的角质化包膜。在这个细胞系中,包膜的最终组装不会自发发生,而是必须使用钙离子载体诱导。在有包膜形成能力和无包膜形成能力的细胞提取物中,分别可以检测到五种潜在的前体蛋白,分子量分别为140K、90K、61K、53K和36K。当使用针对SV - K14细胞纯化角质化包膜的抗血清时,61kD和36kD的前体蛋白在免疫印迹中被特异性标记。通过商业抗兜甲蛋白抗体鉴定出140kD的蛋白为兜甲蛋白。发现部分61kD的蛋白在细胞获得包膜形成能力后插入到质膜中。SV - K14细胞使用的前体蛋白组与文献中描述的体内表皮细胞和体外正常人角质形成细胞的前体蛋白组明显不同。此外,对转化和正常角质形成细胞纯化包膜的溴化氰裂解显示出完全不同的肽图谱。这表明角质化包膜的确切分子组成可能不是严格确定的,并且可能会根据交联酶(与质膜相关的转谷氨酰胺酶)发挥功能时潜在底物蛋白的可用性而有所不同。

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