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整合素αvβ3内化玻连蛋白需要整合素α5β1的连接。

Ligation of integrin alpha5beta1 is required for internalization of vitronectin by integrin alphavbeta3.

作者信息

Pijuan-Thompson V, Gladson C L

机构信息

Department of Pathology, Division of Neuropathology, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.

出版信息

J Biol Chem. 1997 Jan 31;272(5):2736-43. doi: 10.1074/jbc.272.5.2736.

Abstract

Remodeling of the matrix by tumor cells is necessary for tumor invasion. We have shown previously that malignant astrocytomas, in contrast to normal astrocytes, synthesize vitronectin and express integrins alphavbeta3 and alphavbeta5. The activity states of these two integrins are differentially controlled. Thus, we investigated the regulation of the activity of integrins alphavbeta3 and alphavbeta5 with regard to their role in vitronectin internalization in U-251MG astrocytoma cell monolayers adherent to fibronectin, collagen, or laminin in serum-free conditions. Binding of [125I]vitronectin occurred in a specific, saturable manner that was partially inhibitable by monoclonal antibodies (mAbs) specific for integrins alphavbeta3 or alphavbeta5. Specific, lysosomally-mediated degradation of [125I]vitronectin was detectable at 1 h and increased over the 24-h assay period. The cell substrate affected the rate of turnover of [125I]vitronectin, which was 3.0 ng/min for cells plated on fibronectin but 0.35 ng/min for cells plated on collagen. Furthermore, although mAbs specific for either integrin alphavbeta3 or alphavbeta5 inhibited degradation (30%; combined effect 70%) of [125I]vitronectin by cells plated on fibronectin, only mAb anti-alphavbeta5 inhibited degradation (70-90%) by cells plated on collagen or laminin. To determine the requirement for integrin alpha5beta1 ligation in order for integrin alphavbeta3 to internalize its ligand, cells were plated on mAbs anti-integrin alpha5 or anti-integrin alpha3. When plated on mAb anti-alpha5, mAbs anti-alphavbeta3 and anti-alphavbeta5 both inhibited degradation. However, when plated on mAb anti-alpha3, mAb anti-alphavbeta3 had no effect whereas mAb anti-alphavbeta5 inhibited degradation. These data indicate that a signal from integrin alpha5beta1 is necessary for integrin alphavbeta3 to internalize vitronectin, whereas integrin alphavbeta5 constitutively internalizes vitronectin.

摘要

肿瘤细胞对基质的重塑是肿瘤侵袭所必需的。我们之前已经表明,与正常星形胶质细胞相比,恶性星形细胞瘤能合成玻连蛋白并表达整合素αvβ3和αvβ5。这两种整合素的活性状态受到不同的调控。因此,我们研究了整合素αvβ3和αvβ5的活性调节,以及它们在无血清条件下贴附于纤连蛋白、胶原蛋白或层粘连蛋白的U-251MG星形细胞瘤细胞单层中对玻连蛋白内化的作用。[125I]玻连蛋白的结合以特异性、可饱和的方式发生,并且可被整合素αvβ3或αvβ5的特异性单克隆抗体(mAb)部分抑制。在1小时时可检测到[125I]玻连蛋白的特异性、溶酶体介导的降解,并且在24小时的检测期内有所增加。细胞底物影响[125I]玻连蛋白的周转速率,接种在纤连蛋白上的细胞为3.0纳克/分钟,而接种在胶原蛋白上的细胞为0.35纳克/分钟。此外,虽然整合素αvβ3或αvβ5的特异性mAb抑制接种在纤连蛋白上的细胞对[125I]玻连蛋白的降解(30%;联合作用为70%),但只有抗αvβ5 mAb抑制接种在胶原蛋白或层粘连蛋白上的细胞对[125I]玻连蛋白的降解(70 - 90%)。为了确定整合素αvβ3内化其配体时对整合素α5β1连接的需求,将细胞接种在抗整合素α5或抗整合素α3的mAb上。当接种在抗α5 mAb上时,抗αvβ3和抗αvβ5 mAb均抑制降解。然而,当接种在抗α3 mAb上时,抗αvβ3 mAb无作用,而抗αvβ5 mAb抑制降解。这些数据表明,整合素α5β1发出的信号对于整合素αvβ3内化玻连蛋白是必需的,而整合素αvβ5可组成性地内化玻连蛋白。

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