ten Dijke Peter, Arthur Helen M
Molecular Cell Biology, Leiden University Medical Center, Postbus 9600, 2300 RC Leiden, The Netherlands.
Nat Rev Mol Cell Biol. 2007 Nov;8(11):857-69. doi: 10.1038/nrm2262.
The intracellular mechanism of transforming growth factor-beta (TGFbeta) signalling via kinase receptors and SMAD effectors is firmly established, but recent studies of human cardiovascular syndromes such as Marfan syndrome and pre-eclampsia have refocused attention on the importance of regulating the availability of active extracellular TGFbeta. It seems that elastic extracellular matrix (ECM) components have a crucial role in controlling TGFbeta signalling, while soluble and membrane bound forms of TGFbeta co-receptors add further layers of regulation. Together, these extracellular interactions determine the final bioavailability of TGFbeta to vascular cells, and dysregulation is associated with an increasing number of vascular pathologies.
转化生长因子-β(TGFβ)通过激酶受体和SMAD效应器进行信号传导的细胞内机制已得到明确确立,但最近对诸如马凡综合征和先兆子痫等人类心血管综合征的研究,已将注意力重新聚焦于调节活性细胞外TGFβ可用性的重要性上。似乎弹性细胞外基质(ECM)成分在控制TGFβ信号传导中起着关键作用,而TGFβ共受体的可溶性和膜结合形式则增加了更多层次的调节。这些细胞外相互作用共同决定了TGFβ对血管细胞的最终生物可用性,而调节异常与越来越多的血管病变相关。