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子宫内胎儿伤口中F-肌动蛋白的差异表达。

Differential expression of F-actin in in utero fetal wounds.

作者信息

Cowin Allison J

机构信息

Child Health Research Institute, Women's and Children's Hospital, 72 King William Road, North Adelaide, SA, 5006, Australia.

出版信息

Eur J Dermatol. 2005 May-Jun;15(3):133-9.

Abstract

Fetal skin possesses the capacity to heal a wound by a process of regeneration rather than repair, resulting in the absence of scar formation. The actin cytoskeleton may be involved in this process of scar-free wound healing. The effect of wounding on the expression of contractile filamentous actin (F-actin) was investigated in utero in mice between embryonic day 16 (E16) and embryonic day 18 (E18). Increased F-actin staining in the epidermis of the E16 fetal wounds was observed as early as 3 hours post-wounding, peaking in intensity after 24 hours. By 48 hours the intensity of staining had returned to background levels. In marked contrast, E18 fetal wounds did not show increased epidermal F-actin fluorescence, instead increased staining was observed in cells lying perpendicular to the wound margin within the dermis. This developmental switch from epidermal actin expression in "scar-free" fetal wounds to dermal actin expression in late "scar-forming" gestation wounds may be important in fetal wound contraction and scar-free wound repair.

摘要

胎儿皮肤具有通过再生而非修复过程愈合伤口的能力,从而不会形成疤痕。肌动蛋白细胞骨架可能参与了这种无疤痕伤口愈合过程。在胚胎第16天(E16)至胚胎第18天(E18)的小鼠子宫内,研究了创伤对收缩性丝状肌动蛋白(F-肌动蛋白)表达的影响。早在创伤后3小时,就观察到E16胎儿伤口表皮中F-肌动蛋白染色增加,24小时后强度达到峰值。到48小时,染色强度已恢复到背景水平。与之形成鲜明对比的是,E18胎儿伤口未显示表皮F-肌动蛋白荧光增加,而是在真皮内与伤口边缘垂直的细胞中观察到染色增加。这种从“无疤痕”胎儿伤口中的表皮肌动蛋白表达向晚期“形成疤痕”妊娠伤口中的真皮肌动蛋白表达的发育转变,可能在胎儿伤口收缩和无疤痕伤口修复中起重要作用。

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