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Integrin recognition of different cell-binding fragments of laminin (P1, E3, E8) and evidence that alpha 6 beta 1 but not alpha 6 beta 4 functions as a major receptor for fragment E8

机译:整合素识别层粘连蛋白(P1,E3,E8)的不同细胞结合片段,并证明α6beta 1但不是α6beta 4充当片段E8的主要受体

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摘要

The involvement of integrins in mediating interaction of cells to well- characterized proteolytic fragments (P1, E3, and E8) of laminin was assessed by antibody blocking studies. Cell adhesion to fragment P1 was affected by mAbs against the integrin beta 1 and beta 3 subunits and furthermore could be prevented completely by a synthetic peptide containing the Arg-Gly-Asp sequence. Because the beta 3 antibody- sensitive cell lines expressed the vitronectin receptor (alpha v beta 3) at high levels, the involvement of this receptor in cell adhesion to P1 is strongly suggested. Integrin-mediated cell adhesion to E3 is of low affinity and was inhibited by antibodies against the integrin beta 1 subunit. In contrast, adhesion of some cell types to E3 was not or only partially sensitive to inhibition by anti-integrin subunit antibodies. Cell adhesion to E8 was blocked completed by integrin alpha 6 or beta 1 antibodies. The alpha 6-specific antibody did not inhibit cell adhesion to E3 or P1. Furthermore, the antibody only blocked adhesion to laminin of those cells that adhered exclusively to the E8 fragment. In addition, expression of alpha 6 beta 1 was closely correlated with the ability of cells to bind to the E8 fragment of laminin. These results indicate that the alpha 6 beta 1 integrin is a specific receptor for the E8 fragment of laminin. Many cell types expressed, instead of or in addition to alpha 6 beta 1 the recently described integrin alpha 6 beta 4. Although the ligand of alpha 6 beta 4 was not identified, it must be different from that of alpha 6 beta 1, because cells that express alpha 6 beta 4, but not alpha 6 beta 1, do not adhere to E8, and cell adhesion to E8 was specifically blocked by beta 1 specific antibodies. In conclusion, the data indicate that distinct integrin receptors belonging to the beta 1 or beta 3 subfamily are involved in adhesion of cells to the various laminin fragments. Adhesion to E3 may also be brought about by other receptor molecules, possibly proteoglycans, not belonging to the integrin family.
机译:通过抗体阻断研究评估了整合素在介导细胞与层粘连蛋白的特征明确的蛋白水解片段(P1,E3和E8)相互作用中的参与。细胞对片段P1的粘附受到mAb对抗整联蛋白β1和β3亚基的影响,此外,可以通过含有Arg-Gly-Asp序列的合成肽完全阻止。由于β3抗体敏感性细胞系高水平表达玻连蛋白受体(αvβ3),因此强烈建议该受体参与细胞对P1的粘附。整合素介导的细胞与E3的亲和力很低,并被针对整合素β1亚基的抗体所抑制。相反,某些细胞类型对E3的粘附对抗整联蛋白亚基抗体的抑制作用不敏感或仅部分敏感。细胞对E8的粘附被整联蛋白alpha 6或beta 1抗体阻断。 α6特异性抗体不抑制细胞对E3或P1的粘附。此外,该抗体仅阻断仅粘附于E8片段的那些细胞对层粘连蛋白的粘附。此外,α6beta 1的表达与细胞结合层粘连蛋白E8片段的能力密切相关。这些结果表明,α6β1整联蛋白是层粘连蛋白E8片段的特异性受体。除了最近描述的整联蛋白α6beta 4之外,α6beta 1替代或除了α6 beta 1以外还表达了许多细胞类型。尽管未鉴定出α6 beta 4的配体,但它必须与α6 beta 1的配体不同,因为细胞表达α6 beta 4而不表达α6 beta 1的蛋白不粘附于E8,并且细胞对E8的粘附被β1特异性抗体特异性阻断。总之,数据表明属于β1或β3亚家族的独特整合素受体参与细胞与各种层粘连蛋白片段的粘附。对E3的粘附也可能是由不属于整联蛋白家族的其他受体分子(可能是蛋白聚糖)引起的。

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