國家衛生研究院 NHRI:Item 3990099045/10976
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    題名: Differential regulations of fibronectin and laminin in Smad2 activation in vascular endothelial cells in response to disturbed flow
    作者: Yang, TL;Lee, PL;Lee, DY;Wang, WL;Wei, SY;Lee, CI;Chiu, JJ
    貢獻者: Institute of Cellular and Systems Medicine
    摘要: BACKGROUND: Atherosclerosis occurs in arterial curvatures and branches, where the flow is disturbed with low and oscillatory shear stress (OSS). The remodeling and alterations of extracellular matrices (ECMs) and their composition is the critical step in atherogenesis. In this study, we investigated the effects of different ECM proteins on the regulation of mechanotransduction in vascular endothelial cells (ECs) in response to OSS. METHODS: Through the experiments ranging from in vitro cell culture studies on effects of OSS on molecular signaling to in vivo examinations on clinical specimens from patients with coronary artery disease (CAD), we elucidated the roles of integrins and different ECMs, i.e., fibronectin (FN) and laminin (LM), in transforming growth factor (TGF)-beta receptor (TbetaR)-mediated Smad2 activation and nuclear factor-kappaB (NF-kappaB) signaling in ECs in response to OSS and hence atherogenesis. RESULTS: OSS at 0.5+/-12 dynes/cm(2) induces sustained increases in the association of types I and II TbetaRs with beta1 and beta3 integrins in ECs grown on FN, but it only transient increases in ECs grown on LM. OSS induces a sustained activation of Smad2 in ECs on FN, but only a transient activation of Smad2 in ECs on LM. OSS-activation of Smad2 in ECs on FN regulates downstream NF-kappaB signaling and pro-inflammatory gene expression through the activation of beta1 integrin and its association with TbetaRs. In contrast, OSS induces transient activations of beta1 and beta3 integrins in ECs on LM, which associate with type I TbetaR to regulate Smad2 phosphorylation, resulting in transient induction of NF-kappaB and pro-inflammatory gene expression. In vivo investigations on diseased human coronary arteries from CAD patients revealed that Smad2 is highly activated in ECs of atherosclerotic lesions, which is accompanied by the concomitant increase of FN rather than LM in the EC layer and neointimal region of atherosclerotic lesions. CONCLUSIONS: Our findings provide new insights into the mechanisms of how OSS regulates Smad2 signaling and pro-inflammatory genes through the complex signaling networks of integrins, TbetaRs, and ECMs, thus illustrating the molecular basis of regional pro-inflammatory activation within disturbed flow regions in the arterial tree.
    日期: 2018-01-02
    關聯: Journal of Biomedical Science. 2018 Jan 2;25(1):Article number 1.
    Link to: http://dx.doi.org/10.1186/s12929-017-0402-4
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1021-7770&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000419156700001
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85040053979
    顯示於類別:[裘正健] 期刊論文

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