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纯化的表皮五肽可抑制培养的小鼠表皮细胞增殖并增强其终末分化。

Purified epidermal pentapeptide inhibits proliferation and enhances terminal differentiation in cultured mouse epidermal cells.

作者信息

Elgjo K, Reichelt K L, Hennings H, Michael D, Yuspa S H

出版信息

J Invest Dermatol. 1986 Nov;87(5):555-8. doi: 10.1111/1523-1747.ep12455733.

Abstract

Skin extracts contain an epidermal mitosis inhibitor that recently has been purified and identified as a pentapeptide. To develop an in vitro assay system for further biologic characterization, primary mouse epidermal cells and an established mouse epidermal cell line (line 308) were used for testing of the purified pentapeptide. In primary cell cultures the mitotic activity, as estimated by means of vinblastine, was reversibly inhibited by 44% at a peptide concentration of 10(-8) M in high-calcium (1.2 mM Ca++), and by 27-38% at peptide concentrations of 10(-10) and 10(-8) M in low-calcium (0.02 mM Ca++) medium. The 308 cells were inhibited by 46% at a peptide concentration of 10(-6) M but only after the cells had reached near-confluence and had a moderate rate of proliferation. A low concentration of adrenaline (0.18 micrograms/ml) in the medium rendered the primary cultures more sensitive to the peptide. After repeated peptide treatments over 24 h, the number of cornified envelopes (a marker of terminal differentiation) was increased both in primary cultures and in the 308 cells. The epidermal pentapeptide thus seems to influence both proliferation and terminal differentiation in cultured mouse epidermal cells.

摘要

皮肤提取物含有一种表皮有丝分裂抑制剂,最近已被纯化并鉴定为一种五肽。为了开发一种体外检测系统以进行进一步的生物学特性分析,原代小鼠表皮细胞和一种已建立的小鼠表皮细胞系(308系)被用于测试纯化的五肽。在原代细胞培养中,通过长春碱估计的有丝分裂活性,在高钙(1.2 mM Ca++)条件下,肽浓度为10(-8) M时可逆性抑制44%,在低钙(0.02 mM Ca++)培养基中,肽浓度为10(-10)和10(-8) M时抑制27 - 38%。308细胞在肽浓度为10(-6) M时被抑制46%,但仅在细胞达到接近汇合且增殖速率适中之后。培养基中低浓度的肾上腺素(0.18微克/毫升)使原代培养物对该肽更敏感。在24小时内重复进行肽处理后,原代培养物和308细胞中角质化包膜(终末分化的标志物)的数量均增加。因此,表皮五肽似乎影响培养的小鼠表皮细胞的增殖和终末分化。

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