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Identification of PDGF-BB binding to thymosin beta(4) by chemical cross-linking

机译:通过化学交联鉴定PDGF-BB与胸腺素β(4)的结合

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Introduction: The purpose of our work was to identify unknown interaction partners of thymosin beta(4) (T beta(4)). It was suggested that T beta(4) could be an antifibrotic drug for treatment of liver fibrogenesis, because T beta(4) prevents the platelet-derived growth factor-BB (PDGF-BB)-induced activation of hepatic stellate cells (HSCs). Very little information is available how T beta(4) counteracts the PDGF-BB-induced activation of HSCs. We propose the hypothesis that T beta(4) could bind directly to PDGF-BB and thereby reduce the concentration of free PDGF-BB available for binding to the PDGF-beta receptor.
机译:简介:我们工作的目的是确定胸腺素beta(4)(T beta(4))的未知相互作用伙伴。有人提出,T beta(4)可能是治疗肝纤维化的抗纤维化药物,因为T beta(4)阻止了血小板衍生的生长因子-BB(PDGF-BB)诱导的肝星状细胞(HSCs)活化。 。 Tβ(4)如何抵消PDGF-BB诱导的HSC激活的信息很少。我们提出以下假设:T beta(4)可以直接与PDGF-BB结合,从而降低可用于与PDGF-β受体结合的游离PDGF-BB的浓度。

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