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转化生长因子β1对人角质形成细胞体外再上皮化的影响:一种器官型模型

Effect of TGF-beta 1 on re-epithelialization of human keratinocytes in vitro: an organotypic model.

作者信息

Garlick J A, Taichman L B

机构信息

Department of Oral Biology and Pathology, School of Dental Medicine, State University of New York at Stony Brook 11794-8702.

出版信息

J Invest Dermatol. 1994 Oct;103(4):554-9. doi: 10.1111/1523-1747.ep12396847.

Abstract

Transforming growth factor beta-1 (TGF-beta 1) has been shown to inhibit keratinocyte proliferation in vitro yet and migration was investigated in organotypic cultures after incisional wounding. Organotypic cultures provide a more in vivo-like epidermal tissue and may therefore respond in a different manner than previous culture models in which epidermal differentiation is incomplete. Without TGF-beta 1, keratinocytes were hyperproliferative in response to wounding. At doses of 2.5 ng/ml or greater, a delay in re-epithelialization was seen at 24 h post-wounding along with a reduction in hyperproliferation. By 48 h, however, re-epithelialization was complete in all cultures treated with TGF-beta 1. In particular, 7 ng/ml TGF-beta 1 inhibited proliferation yet had no effect on re-epithelialization by 48 h. These studies demonstrate that i) TGF-beta 1 induced a delay in re-epithelialization, ii) proliferation of wounded keratinocytes was not inhibited at 2.5 ng/ml doses of TGF-beta 1, and iii) at 7 ng/ml TGF-beta 1, re-epithelialization was complete by 48 h in spite of the profound inhibition of cell proliferation. In the organotypic model, TGF-beta 1 appears to alter re-epithelialization.

摘要

转化生长因子β-1(TGF-β1)已被证明在体外可抑制角质形成细胞增殖,并且在切开伤口后的器官型培养中对其迁移进行了研究。器官型培养提供了更接近体内的表皮组织,因此其反应方式可能与之前表皮分化不完全的培养模型不同。在没有TGF-β1的情况下,角质形成细胞对伤口产生过度增殖反应。在2.5 ng/ml或更高剂量时,受伤后24小时可见再上皮化延迟,同时过度增殖减少。然而,到48小时时,所有用TGF-β1处理的培养物中再上皮化均已完成。特别是,7 ng/ml的TGF-β1抑制增殖,但到48小时时对再上皮化没有影响。这些研究表明:i)TGF-β1导致再上皮化延迟;ii)在2.5 ng/ml剂量的TGF-β1下,受伤角质形成细胞的增殖未受抑制;iii)在7 ng/ml的TGF-β1下,尽管细胞增殖受到显著抑制,但到48小时时再上皮化已完成。在器官型模型中,TGF-β1似乎改变了再上皮化过程。

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