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白细胞介素-1α通过一条不依赖表皮生长因子/转化生长因子-α的途径刺激角质形成细胞迁移。

Interleukin-1 alpha stimulates keratinocyte migration through an epidermal growth factor/transforming growth factor-alpha-independent pathway.

作者信息

Chen J D, Lapiere J C, Sauder D N, Peavey C, Woodley D T

机构信息

Department of Dermatology, Northwestern University School of Medicine, Chicago, IL 60611, USA.

出版信息

J Invest Dermatol. 1995 May;104(5):729-33. doi: 10.1111/1523-1747.ep12606970.

Abstract

Epidermal growth factor (EGF) and transforming growth factor-alpha (TGF-alpha) stimulate keratinocyte migration on collagen by up-regulating the alpha 2 subunit of the collagen integrin, alpha 2 beta 1. Interleukin-1 (IL-1) is an autocrine factor, produced by keratinocytes themselves, that is modulated by ultraviolet light and increases the proliferative potential of keratinocytes in culture. The autocrine nature of keratinocyte-derived IL-1 alpha is emphasized by the fact that it induces the keratinocyte to synthesize IL-1 alpha and TGF-alpha, a cytokine known to induce keratinocyte motility. Further, topical application of IL-1 alpha has been shown to promote wound healing in animals. In this study, we used a well-defined keratinocyte migration assay to assess the effect of IL-1 alpha on keratinocyte motility and to examine whether the IL-1 alpha/TGF alpha pathway is involved. The addition of recombinant human IL-1 alpha to keratinocytes produced a statistically significant and concentration-dependent increase in migration on matrices of collagen types I and IV, but not on laminin. Maximal levels of keratinocyte migration obtained on these matrices with IL-1 alpha were comparable to those obtained with stimulation by EGF and TGF-alpha. The effects of TGF-alpha and IL-1 alpha on keratinocyte migration are additive; however, the maximal level of migration achieved by using IL-1 alpha and TGF-alpha in combination never exceeds the maximal level of migration found by using either cytokine alone. The time course of keratinocyte migration induced by IL-1 alpha is delayed (onset of migration 9-12 h after addition) as compared with that induced by TGF-alpha (onset of migration 6-9 h after addition) even if the cells are preincubated in IL-1 alpha. Flow cytometry analysis demonstrated no change in surface expression of integrin subunits, specifically that of integrin subunit alpha 2, previously shown to be up-regulated by EGF/TGF-alpha. These results suggest that IL-1 alpha stimulates keratinocyte migration on collagen via a mechanism distinct from that of EGF/TGF-alpha.

摘要

表皮生长因子(EGF)和转化生长因子-α(TGF-α)通过上调胶原整合素α2β1的α2亚基,刺激角质形成细胞在胶原蛋白上迁移。白细胞介素-1(IL-1)是角质形成细胞自身产生的一种自分泌因子,受紫外线调节,并增加培养中角质形成细胞的增殖潜能。角质形成细胞衍生的IL-1α的自分泌性质体现在它能诱导角质形成细胞合成IL-1α和TGF-α,TGF-α是一种已知能诱导角质形成细胞运动的细胞因子。此外,局部应用IL-1α已被证明能促进动物伤口愈合。在本研究中,我们使用一种明确的角质形成细胞迁移试验来评估IL-1α对角质形成细胞运动的影响,并检查IL-1α/TGF-α途径是否参与其中。将重组人IL-1α添加到角质形成细胞中,可使角质形成细胞在I型和IV型胶原基质上的迁移产生统计学上显著的浓度依赖性增加,但在层粘连蛋白上则无此作用。用IL-1α在这些基质上获得的角质形成细胞迁移的最大水平与用EGF和TGF-α刺激获得的水平相当。TGF-α和IL-1α对角质形成细胞迁移的作用是相加的;然而,联合使用IL-1α和TGF-α实现的最大迁移水平从未超过单独使用任何一种细胞因子所发现的最大迁移水平。与TGF-α诱导的角质形成细胞迁移(添加后6-9小时开始迁移)相比,IL-1α诱导的角质形成细胞迁移的时间进程延迟(添加后9-12小时开始迁移),即使细胞预先在IL-1α中孵育。流式细胞术分析表明,整合素亚基的表面表达没有变化,特别是整合素亚基α2的表达,先前已证明其受EGF/TGF-α上调。这些结果表明,IL-1α通过一种不同于EGF/TGF-α的机制刺激角质形成细胞在胶原蛋白上迁移。

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