Carter W G, Wayner E A, Bouchard T S, Kaur P
Fred Hutchinson Cancer Research Center, Seattle, Washington 98104.
J Cell Biol. 1990 Apr;110(4):1387-404. doi: 10.1083/jcb.110.4.1387.
We have examined cultures of neonatal human foreskin keratinocytes (HFKs) to determine the ligands and functions of integrins alpha 2 beta 1, and alpha 3 beta 1 in normal epidermal stratification and adhesion to the basement membrane zone (BMZ) in skin. We used three assay systems, HFK adhesion to purified extracellular matrix (ECM) ligands and endogenous secreted ECM, localization of integrins in focal adhesions (FAs), and inhibition of HFK adhesion with mAbs to conclude: (a) A new anti-alpha 3 beta 1 mAb, P1F2, localized alpha 3 beta 1 in FAs on purified laminin greater than fibronectin/collagen, indicating that laminin was the best exogeneous ligand for alpha 3 beta 1. However, in long term culture, alpha 3 beta 1 preferentially codistributed in and around FAs with secreted laminin-containing ECM, in preference to exogenous laminin. Anti-alpha 3 beta 1, mAb P1B5, detached prolonged cultures of HFKs from culture plates or from partially purified HFK ECM indicating that interaction of alpha 3 beta 1 with the secreted laminin-containing ECM was primarily responsible for HFK adhesion in long term culture. (b) In FA assays, alpha 2 beta 1 localized in FAs conincident with initial HFK adhesion to exogenous collagen, but not laminin or fibronectin. However, in inhibition assays, anti-alpha 2 beta 1 inhibited initial HFK adhesion to both laminin and collagen. Thus, alpha 2 beta 1 contributes to initial HFK adhesion to laminin but alpha 3 beta 1 is primarily responsible for long-term HFK adhesion to secreted laminin-containing ECM. (c) Serum or Ca2(+)-induced aggregation of HFKs resulted in relocation of alpha 2 beta 1 and alpha 3 beta 1 from FAs to cell-cell contacts. Further, cell-cell adhesion was inhibited by anti-alpha 3 beta 1 (P1B5) and a new anti-beta 1 mAb (P4C10). Thus, interaction of alpha 3 beta 1 with either ECM or membrane coreceptors at cell-cell contacts may facilitate Ca2(+)-induced HFK aggregation. (d) It is suggested that interaction of alpha 3 beta 1 with a secreted, laminin-containing ECM in cultured HFKs, duplicates the role of alpha 3 beta 1 in basal cell adhesion to the BMZ in skin. Further, relocation of alpha 2 beta 1 and alpha 3 beta 1 to cell-cell contacts may result in detachment of cells from the BMZ and increased cell-cell adhesion in the suprabasal cells contributing to stratification of the skin.
我们检测了新生儿人包皮角质形成细胞(HFKs)的培养物,以确定整合素α2β1和α3β1在正常表皮分层以及皮肤中与基底膜带(BMZ)黏附过程中的配体和功能。我们使用了三种检测系统:HFKs与纯化的细胞外基质(ECM)配体及内源性分泌的ECM的黏附、整合素在黏着斑(FAs)中的定位,以及用单克隆抗体抑制HFKs的黏附,从而得出以下结论:(a)一种新的抗α3β1单克隆抗体P1F2,将α3β1定位在纯化层粘连蛋白上的黏着斑中,其定位程度大于纤连蛋白/胶原蛋白,表明层粘连蛋白是α3β1的最佳外源性配体。然而,在长期培养中,α3β1优先与分泌的含层粘连蛋白的ECM在黏着斑及其周围共分布,而不是与外源性层粘连蛋白。抗α3β1单克隆抗体P1B5使长期培养的HFKs从培养板或部分纯化的HFK ECM上脱离,这表明α3β1与分泌的含层粘连蛋白的ECM的相互作用是长期培养中HFKs黏附的主要原因。(b)在黏着斑检测中,α2β1定位在与HFKs最初黏附到外源性胶原蛋白相关的黏着斑中,但不与层粘连蛋白或纤连蛋白相关。然而,在抑制检测中,抗α2β1抑制了HFKs最初对层粘连蛋白和胶原蛋白的黏附。因此,α2β1有助于HFKs最初对层粘连蛋白的黏附,但α3β1是HFKs长期黏附到分泌的含层粘连蛋白的ECM的主要原因。(c)血清或Ca2⁺诱导的HFKs聚集导致α2β1和α3β1从黏着斑重新定位到细胞 - 细胞接触部位。此外,抗α3β1(P1B5)和一种新的抗β1单克隆抗体(P4C10)抑制了细胞 - 细胞黏附。因此,α3β1与细胞 - 细胞接触部位的ECM或膜共受体的相互作用可能促进Ca2⁺诱导的HFKs聚集。(d)有人提出,在培养的HFKs中,α3β1与分泌的含层粘连蛋白的ECM的相互作用,类似于α3β1在皮肤基底细胞与BMZ黏附中的作用。此外,α2β1和α3β1重新定位到细胞 - 细胞接触部位可能导致细胞从BMZ脱离,并增加基底上层细胞间的黏附,从而有助于皮肤分层。