国家重点基础研究发展规划资助项目(G1999055903)和中国科学院知识创新工程基金资助项目.
This work was supported by grants from The Special Funds for Major State Basic Research Project (G1999055903) and The Knowledge Innovation Project of The Chinese Academy of Sciences.
基质金属蛋白酶 (MMPs) 及其组织抑制因子 (TIMPs) 参与调控胞外基质 (ECM) 的降解与重建,二者的协同作用以及表达的动态平衡保证组织的生理/病理形态结构建成,并完成生长、分化、维持、降解的往复周期. 转化生长因子-β(TGF-β)通过对MMPs和TIMPs家族成员因细胞类型而异的基因表达调控作用,表现出调节ECM重建的生物学效应. TGF-β可通过激活Smad通路、促分裂原活化蛋白激酶 (MAPK) 通路,以及刺激激活蛋白-1(AP-1)复合体的形成,完成对MMPs和TIMPs基因表达的调控功能.
Matrix metalloproteinases (MMPs) and tissue inhibitors of MMPs (TIMPs) play pivotal roles in the degradation and remodeling of the extracellular matrix (ECM). The cooperation and balanced expressions of MMPs and TIMPs are essential issues for the cyclic growth, differentiation, maintenance, and degradation of the tissues during physiologic and pathologic processes. Transforming growth factor-β (TGF-β) could perform its biological effect on ECM by regulating the gene expressions of MMPs and TIMPs. The different modulating effects of TGF-β on MMPs and TIMPs in different cell types are due to the activating of Smad pathway, MAPK signaling pathway or inducing the formation of AP-1 complex by extracellular TGF-β signal.
林海燕,王红梅,祝诚.转化生长因子-β对基质金属蛋白酶及其组织抑制因子调控的研究进展[J].生物化学与生物物理进展,2003,30(1):7-12
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