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胶带剥离可诱导非皮损性银屑病皮肤出现显著的表皮增生并改变转化生长因子-α(TGF-α)的表达。

Tape stripping induces marked epidermal proliferation and altered TGF-alpha expression in non-lesional psoriatic skin.

作者信息

Hatta N, Takata M, Kawara S, Hirone T, Takehara K

机构信息

Department of Dermatology, Kanazawa University School of Medicine, Takara-machi, Japan.

出版信息

J Dermatol Sci. 1997 Feb;14(2):154-61. doi: 10.1016/s0923-1811(96)00567-1.

Abstract

Psoriasis is a chronic inflammatory disorder characterized by epidermal hyperproliferation. Although recent evidence suggests that T cell activation is a primary trigger for psoriasis lesions, there may be alterations in the keratinocyte growth regulatory pathways which induce epidermal hyperproliferation in psoriatic patients. To test this hypothesis, we investigated the proliferative activity of epidermal keratinocytes 48 h after tape stripping, one of the standard mechanical ways to stimulate the epidermis, in 20 psoriasis patients and in 18 controls. Epidermal cell kinetics were assessed with DNA flow cytometry, the mitotic index, bromodeoxyuridine incorporation, Ki-67 antigen expression and DNA polymerase alpha expression. The expression of TGF-alpha and EGF receptors, critical mediators of keratinocyte proliferation, were also investigated immunohistochemically. The results of multiparameter assays showed that the baseline proliferative activity in uninvolved skin was the same in psoriasis patients and normal controls. After tape stripping, although both psoriasis patients and the normal controls showed significant increases in epidermal cell proliferation, the values of all the parameters investigated were significantly greater in the psoriasis patients than in the normal controls. EGF receptors were overexpressed in basal and suprabasal keratinocytes after tape stripping in both the psoriasis patients and the normal controls. In contrast, overexpression of TGF-alpha was only observed in the patients with psoriasis, which may explain their increased proliferative response to trauma.

摘要

银屑病是一种以表皮过度增殖为特征的慢性炎症性疾病。尽管最近的证据表明T细胞活化是银屑病皮损的主要触发因素,但银屑病患者角质形成细胞生长调节途径可能存在改变,从而导致表皮过度增殖。为了验证这一假设,我们对20例银屑病患者和18例对照者进行了研究,采用胶带剥离(一种刺激表皮的标准机械方法)后48小时,检测表皮角质形成细胞的增殖活性。通过DNA流式细胞术、有丝分裂指数、溴脱氧尿苷掺入、Ki-67抗原表达和DNA聚合酶α表达来评估表皮细胞动力学。还通过免疫组织化学研究了角质形成细胞增殖的关键介质TGF-α和EGF受体的表达。多参数分析结果显示,银屑病患者和正常对照者未受累皮肤的基线增殖活性相同。胶带剥离后,尽管银屑病患者和正常对照者的表皮细胞增殖均显著增加,但银屑病患者所有检测参数的值均显著高于正常对照者。胶带剥离后,银屑病患者和正常对照者的基底和基底上层角质形成细胞中EGF受体均过度表达。相比之下,仅在银屑病患者中观察到TGF-α的过度表达,这可能解释了他们对创伤的增殖反应增加。

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