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肿瘤坏死因子-α可增加人皮肤成纤维细胞中整合素α2β1的表达以及细胞与I型胶原的黏附。

Tumor necrosis factor-alpha increased the integrin alpha 2 beta 1 expression and cell attachment to type I collagen in human dermal fibroblasts.

作者信息

Ezoe K, Horikoshi T

机构信息

Department of Dermatology, Sapporo Medical College, Japan.

出版信息

Biochem Biophys Res Commun. 1993 Apr 15;192(1):281-7. doi: 10.1006/bbrc.1993.1411.

Abstract

Cell adhesion molecules of human dermal fibroblasts play an important role in the processes of wound healing. The effects of tumor necrosis factor- alpha (TNF) on the expression of integrin beta 1 subfamily in human dermal fibroblasts were examined. TNF preferentially induced the expression of alpha 2 beta 1 integrins, receptors for collagen and laminin, in a time and dose dependent manner. Cell attachment to type I collagen increased by the treatment with TNF. However, cell attachment to fibronectin and laminin was not increased. This TNF-induced cell attachment could be reduced significantly by anti-integrin alpha 2 beta 1 antibody. Antibodies against receptors other than alpha 2 beta 1 integrin did not significantly reduce cell attachment. These data suggest that the increased attachment of human dermal fibroblasts to type I collagen appears to be mediated predominantly through the augmentation of integrin alpha 2 beta 1 expression by TNF.

摘要

人真皮成纤维细胞的细胞黏附分子在伤口愈合过程中起重要作用。研究了肿瘤坏死因子-α(TNF)对人真皮成纤维细胞中整合素β1亚家族表达的影响。TNF以时间和剂量依赖性方式优先诱导α2β1整合素(胶原蛋白和层粘连蛋白的受体)的表达。用TNF处理可增加细胞与I型胶原蛋白的黏附。然而,细胞与纤连蛋白和层粘连蛋白的黏附并未增加。这种TNF诱导的细胞黏附可被抗整合素α2β1抗体显著降低。针对α2β1整合素以外的受体的抗体并未显著降低细胞黏附。这些数据表明,人真皮成纤维细胞与I型胶原蛋白黏附的增加似乎主要是通过TNF增强整合素α2β1的表达介导的。

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