A transmembrane extracellular matrix receptor of the integrin family, alpha 6 beta 4, is a component of the hemidesmosome, an adhesion complex of importance in epithelial cell-connective tissue attachment (Stepp, M. A., S. Spurr-Michaud, A. Tisdale, J. Elwell, and I. K. Gipson. 1990. Proc. Natl. Acad. Sci. USA. 87:8970-8974; Jones, J. C. R., M. A. Kurpakus, H. M. Cooper, and V. Quaranta. 1991. Cell Regulation. 2:427-438). Cytosolic components of hemidesmosomes include bullous pemphigoid (BP) antigens while extracellular components include a 125-kD component of anchoring filaments (CAF) and collagen type VII-containing anchoring fibrils. We have monitored the incorporation of the alpha 6 beta 4 integrins into forming hemidesmosomes in an in vitro wound-healing explant model. In epithelial cells recently migrated from the edges of unwounded sites over bare connective tissue, alpha 6 beta 4 first appears along the entire cell surface. At this stage, these cells contain little or no cytosolic hemidesmosomal components, at least as detectable by immunofluorescence using BP autoantibodies, whereas they are already positive for laminin and CAF. At a later stage, as cells become positive for cytosolic hemidesmosome components such as BP antigens as well as collagen type VII, alpha 6 beta 4 becomes concentrated along the basal pole of the epithelial cell where it abuts the connective tissue of the explant. Polyclonal antibodies to beta 4 do not interfere with the migration of epithelial cells in the explant. However, they prevent assembly of hemidesmosomal complexes and inhibit expression of collagen type VII in cells that have migrated over wound areas. In addition, they induce disruption of established hemidesmosomes in nonmigrating cells of the unwounded area of the explant. Monoclonal antibodies to alpha 6 have a more dramatic effect, since they completely detach epithelial cells in the unwounded area of the explant. Antibodies to CAF also detach epithelial cells in unwounded areas, apparently by inducing separation between epithelium and connective tissue at the lamina lucida of the basement membrane zone. These results suggest a model whereby polarization of alpha 6 beta 4 to the basal surface of the cells, perhaps induced by a putative anchoring filament-associated ligand, triggers assembly of hemidesmosome plaques.

译文

整联蛋白家族的跨膜细胞外基质受体 α6β4是半染色体的组成部分,半染色体是上皮细胞-结缔组织附着中重要的粘附复合物 (Stepp,m.a.,S. Spurr-Michaud,A. Tisdale,J. Elwell,和I. K. Gipson。1990. Proc. Natl. Acad. Sci.美国。87:8970-8974; Jones,j.c.R.,M.Kurpakus,H. M. Cooper和V. Quaranta。1991.细胞调控。2:427-438)。半桥粒的胞质组分包括大疱性类天疱疮 (BP) 抗原,而细胞外组分包括锚定细丝 (CAF) 的125-kD组分和含VII型胶原的锚定原纤维。我们已经在体外伤口愈合外植体模型中监测了 α6β4整合素在形成半桥体中的掺入。在最近从裸露的结缔组织上未受伤部位的边缘迁移的上皮细胞中,α6β4首先出现在整个细胞表面。在这个阶段,这些细胞含有很少或没有胞质半染色体成分,至少可以通过使用BP自身抗体的免疫荧光检测到,而它们已经对层粘连蛋白和CAF呈阳性。在稍后的阶段,随着细胞对胞质半桥粒成分 (例如BP抗原) 以及VII型胶原呈阳性,α6β4沿着上皮细胞的基极集中,并与外植体的结缔组织邻接。针对 β4的多克隆抗体不会干扰外植体中上皮细胞的迁移。但是,它们阻止了半桥粒复合体的组装,并抑制了在伤口区域迁移的细胞中VII型胶原的表达。此外,它们还会诱导外植体未受伤区域的非迁移细胞中已建立的半桥粒的破坏。针对 α6的单克隆抗体具有更显着的作用,因为它们完全脱离了外植体未受伤区域的上皮细胞。针对CAF的抗体也可以通过诱导基底膜区的上皮和结缔组织之间的分离而分离未受伤区域的上皮细胞。这些结果提出了一个模型,其中 α6β4极化到细胞的基底表面,可能是由假定的锚定细丝相关配体诱导的,触发了半桥粒斑块的组装。

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