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迟发型超敏反应中巨噬细胞浸润与表皮形成之间的关系

Relationship between macrophage infiltration and epidermopoiesis in delayed-type hypersensitivity.

作者信息

Tanaka T, Imamura S, Takigawa M

机构信息

Department of Dermatology, Faculty of Medicine, Kyoto University, Japan.

出版信息

Arch Dermatol Res. 1988;280(1):18-22. doi: 10.1007/BF00412683.

Abstract

The relationship between epidermopoiesis and macrophage infiltration was studied in delayed-type hypersensitivity (DTH) skin lesions in guinea pigs that had been sensitized with heat-killed tubercle bacilli or bovine serum albumin (BSA). Macrophages were identified with acid-phosphatase and nonspecific esterase stains, and the epidermal proliferative response was studied at DTH challenge sites by autoradiography. The number of macrophages in the sensitized animals was higher than that in the nonsensitized animals 48-72 h following challenge injections, when labelling indices were also elevated in the former group. Soluble factor(s) from cultured macrophages transiently enhanced the DNA synthesis of epidermal cells in cultures and in the sites injected with the factor(s). These results suggest that macrophages retained in the DTH lesion may play a role in an acceleration of epidermal proliferation, thus leading to acanthosis and lichenification.

摘要

在经热灭活结核杆菌或牛血清白蛋白(BSA)致敏的豚鼠迟发型超敏反应(DTH)皮肤损伤中,研究了表皮形成与巨噬细胞浸润之间的关系。用酸性磷酸酶和非特异性酯酶染色鉴定巨噬细胞,并通过放射自显影术在DTH激发部位研究表皮增殖反应。激发注射后48 - 72小时,致敏动物中的巨噬细胞数量高于未致敏动物,且前一组的标记指数也升高。培养巨噬细胞产生的可溶性因子能短暂增强培养物中及注射该因子部位的表皮细胞DNA合成。这些结果表明,滞留在DTH损伤中的巨噬细胞可能在加速表皮增殖中起作用,从而导致棘皮症和苔藓化。

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