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皮肤伤口愈合中Fas和Fas配体的免疫组织化学研究

Immunohistochemical study on Fas and Fas ligand in skin wound healing.

作者信息

Guan D W, Ohshima T, Kondo T

机构信息

Department of Legal Medicine, Kanazawa University Faculty of Medicine, School of Medicine, Japan.

出版信息

Histochem J. 2000 Feb;32(2):85-91. doi: 10.1023/a:1004058010500.

Abstract

An immunohistochemical study on the expression of Fas and Fas ligand (Fas L) was performed in order to examine the role of apoptosis through Fas-Fas L in mouse skin wound healing. After a 1-cm-long incision in the central dorsum skin, mice were sacrificed at intervals ranging from 0.5 to 240 h, followed by the sampling of wound margin. The expression of Fas and Fas L in the wound margins and in uninjured skin controls was studied using frozen sections. In uninjured skin controls, a very weak expression of Fas and Fas L was detected immunohistochemically in hair follicles, sebaceous glands and epidermal cells. In wounded specimens, polymorphonuclear cells and inflammatory mononuclear ones (round-shaped and spindle-shaped types) were evident. A single immunostaining showed that Fas or Fas L was detectable in inflammatory mononuclear cells involved in the skin wound healing process. Double immunostaining for Fas and Fas L revealed that inflammatory mononuclear cells co-expressed both antigens. In situ TUNEL combined with immunostaining showed that the inflammatory mononuclear cells expressing Fas or Fas L and the polymorphonuclear cells were TUNEL-stained, although neither Fas nor Fas L was detected in the polymorphonuclear cells. The number of TUNEL-positive, inflammatory mononuclear cells expressing Fas or Fas L per 0.01 x 0.01 cm2 was counted. The average number of 10 randomly selected microscope fields reached a peak at the fibro-proliferative phase of wound healing. These results indicate that apoptosis through Fas and Fas L may play an important role for reducing the cellularity during skin wound healing in mice.

摘要

为了研究Fas-Fas配体(Fas L)介导的细胞凋亡在小鼠皮肤伤口愈合中的作用,进行了一项关于Fas和Fas L表达的免疫组织化学研究。在小鼠背部中央皮肤做一个1厘米长的切口后,每隔0.5至240小时处死小鼠,然后取伤口边缘组织样本。使用冰冻切片研究伤口边缘和未受伤皮肤对照中Fas和Fas L的表达。在未受伤的皮肤对照中,免疫组织化学检测到毛囊、皮脂腺和表皮细胞中Fas和Fas L表达非常微弱。在受伤标本中,多形核细胞和炎性单核细胞(圆形和梭形)明显可见。单次免疫染色显示,在参与皮肤伤口愈合过程的炎性单核细胞中可检测到Fas或Fas L。Fas和Fas L的双重免疫染色显示,炎性单核细胞同时表达这两种抗原。原位末端脱氧核苷酸转移酶介导的缺口末端标记法(TUNEL)结合免疫染色显示,表达Fas或Fas L的炎性单核细胞和多形核细胞呈TUNEL阳性染色,尽管在多形核细胞中未检测到Fas和Fas L。计算每0.01×0.01平方厘米中表达Fas或Fas L的TUNEL阳性炎性单核细胞数量。在10个随机选择的显微镜视野中,平均数量在伤口愈合的纤维增殖期达到峰值。这些结果表明,通过Fas和Fas L介导的细胞凋亡可能在小鼠皮肤伤口愈合过程中减少细胞数量方面发挥重要作用。

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