Vernon R B, Angello J C, Iruela-Arispe M L, Lane T F, Sage E H
Department of Biological Structure, University of Washington, Seattle.
Lab Invest. 1992 May;66(5):536-47.
Vascular endothelial cells that are cultured on layers of gelled basement membrane matrix organize rapidly into networks of cords or tubelike structures. Although this phenomenon is a potential model for angiogenesis in vivo, we questioned whether basement membrane matrix directs the differentiation of endothelial cells in a specific manner. In this study, we have examined factors that influence the formation of cellular networks in vitro in an attempt to define a basic mechanism for this process. We found that endothelial cells, fibroblasts, smooth muscle cells, and cells of the murine Leydig cell line TM3 formed networks on basement membrane matrix in much the same fashion. Light and electron microscopy, combined with time-lapse videomicroscopy, revealed that cells organized on a tesselated network of aligned basement membrane matrix that was generated by tension forces of cellular traction. Cellular elongation and progressive motility across the surface of the gel were restricted to tracks of aligned matrix and did not occur until the tracks appeared. The formation of cellular networks on basement membrane matrix was inhibited by reducing the thickness of the matrix, by including native type I collagen in the matrix, or by disrupting cytoskeletal microfilaments and microtubules. Cell division was not required for network formation. Bovine aortic endothelial cells that formed networks did not simultaneously transcribe mRNA for type I collagen, a protein synthesized by endothelial cells that form tubes spontaneously in vitro. Moreover, levels of mRNA for fibronectin and SPARC (Secreted Protein that is Acidic and Rich in Cysteine) in network-forming cells were similar to levels seen in endothelial cells that did not form networks. Endothelial cells and TM3 cells that were plated on highly malleable gels of native type I collagen also formed cords and aligned matrix fibers into linear tracks that resembled those generated on basement membrane matrix, although the structures were not as well-defined. Our observations suggest that the mechanochemical properties of extracellular matrices are able to translate the forces of cellular traction into templates that direct the formation of complex cellular patterns.
在凝胶化的基底膜基质层上培养的血管内皮细胞会迅速组织成索状或管状结构的网络。尽管这种现象是体内血管生成的潜在模型,但我们质疑基底膜基质是否以特定方式指导内皮细胞的分化。在本研究中,我们检查了影响体外细胞网络形成的因素,试图确定这一过程的基本机制。我们发现内皮细胞、成纤维细胞、平滑肌细胞以及小鼠睾丸间质细胞系TM3的细胞以大致相同的方式在基底膜基质上形成网络。光学显微镜和电子显微镜,结合延时视频显微镜,揭示细胞在由细胞牵引力的张力产生的排列的基底膜基质的棋盘状网络上组织起来。细胞在凝胶表面的伸长和渐进性运动仅限于排列的基质轨迹,并且直到轨迹出现才会发生。通过减小基质厚度、在基质中加入天然I型胶原或破坏细胞骨架微丝和微管,可抑制基底膜基质上细胞网络的形成。网络形成不需要细胞分裂。形成网络的牛主动脉内皮细胞不会同时转录I型胶原的mRNA,I型胶原是内皮细胞合成的一种蛋白质,内皮细胞在体外可自发形成管。此外,形成网络的细胞中纤连蛋白和SPARC(富含半胱氨酸的酸性分泌蛋白)的mRNA水平与未形成网络的内皮细胞中的水平相似。接种在高度可塑的天然I型胶原凝胶上的内皮细胞和TM3细胞也形成索状,并将基质纤维排列成线性轨迹,类似于在基底膜基质上产生的轨迹,尽管结构没有那么清晰。我们的观察结果表明,细胞外基质的机械化学性质能够将细胞牵引力转化为指导复杂细胞模式形成的模板。