Nunes I, Munger J S, Harpel J G, Nagano Y, Shapiro R L, Gleizes P E, Rifkin D B
Department of Cell Biology, New York University Medical Center, NY 10016, USA.
Int J Obes Relat Metab Disord. 1996 Mar;20 Suppl 3:S4-8.
Most cell types express transforming growth factor-beta (TGF-beta) as a large latent TGF-beta complex that must be converted to an active form before TGF-beta can interact with cell surface TGF-beta receptors. This conversion involves the release of mature TGF-beta from the complex by disrupting noncovalent interactions between mature TGF-beta and its propeptide, latency associated peptide. A critical step in regulating TGF-beta effects may be the activation of the large latent TGF-beta complex. Activation of the complex can be achieved by chemical and enzymatic treatments, or by various cell systems. We have identified that coculturing bovine endothelial and smooth muscle cells generates active TGF-beta. Coculture activation of the large latent TGF-beta complex occurs through a plasmin-dependent mechanism that requires concentration of reactants on the cell surface and/or extracellular matrix. The mechanism of latent TGF-beta activation self-regulates through effectors of plasmin generation.
大多数细胞类型将转化生长因子-β(TGF-β)表达为一种大的潜伏性TGF-β复合物,在TGF-β能够与细胞表面TGF-β受体相互作用之前,该复合物必须转化为活性形式。这种转化涉及通过破坏成熟TGF-β与其前肽(潜伏相关肽)之间的非共价相互作用,从复合物中释放出成熟TGF-β。调节TGF-β效应的关键步骤可能是大的潜伏性TGF-β复合物的激活。该复合物的激活可以通过化学和酶处理或各种细胞系统来实现。我们已经确定,共培养牛内皮细胞和平滑肌细胞会产生活性TGF-β。大的潜伏性TGF-β复合物的共培养激活通过纤溶酶依赖性机制发生,该机制需要反应物在细胞表面和/或细胞外基质上浓缩。潜伏性TGF-β激活机制通过纤溶酶生成的效应器进行自我调节。