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首页> 外文期刊>The Biochemical Journal >Hepatocyte growth factor activator inhibitor type 2 (HAI-2) modulates hepcidin expression by inhibiting the cell surface protease matriptase-2
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Hepatocyte growth factor activator inhibitor type 2 (HAI-2) modulates hepcidin expression by inhibiting the cell surface protease matriptase-2

机译:2型肝细胞生长因子激活因子抑制剂(HAI-2)通过抑制细胞表面蛋白酶matriptase-2来调节hepcidin表达

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Matriptase-2, a recently identified cell surface protease, is the key enzyme of iron homoeostasis modulating the expression of the liver peptide hormone hepcidin. HAT (hepatocyte growth factor activator inhibitor) types 1 and 2 (HAI-1 and HAI-2 respectively) have been shown to inhibit the close homologue, i.e. matriptase. By co-expressing matriptase-2 and the inhibitor HAI-2 we have identified HAI-2 displaying high inhibitory potential against matriptase-2 at the cell surface as well as in conditioned medium. Accordingly, complex formation between matriptase-2 and HAI-2 was demonstrated by isolation of the complex via immobilizing either HAI-2 or matriptase-2 from lysates and conditioned medium of co-expressing cells. Furthermore, HAI-2 indirectly influences the expression of the hepcidin-encoding gene HAMP. The inhibitor abrogates the matriptase-2-mediated suppression of HAMP expression, presumably by inhibiting the supposed potential of matriptase-2 to cleave membrane-bound HJV (haemojuvelin). Taken together, the results of the present study have characterized HAI-2 as an inhibitor of matriptase-2 that modulates the synthesis of hepcidin and provides new insights into the regulatory mechanism of iron homoeostasis, with clinical importance for a treatment of iron overload diseases.
机译:Matriptase-2是最近发现的一种细胞表面蛋白酶,是铁均位调节肝肽激素hepcidin表达的关键酶。已显示1型和2型HAT(肝细胞生长因子激活剂抑制剂)(分别为HAI-1和HAI-2)可抑制紧密同源物,即matriptase。通过共表达matriptase-2和抑制剂HAI-2,我们已经鉴定出HAI-2在细胞表面以及条件培养基中均显示出对matriptase-2的高抑制潜力。因此,通过从共表达细胞的裂解物和条件培养基中固定HAI-2或matriptase-2来分离复合物,证明了matriptase-2和HAI-2之间的复合物形成。此外,HAI-2间接影响铁调素编码基因HAMP的表达。该抑制剂消除了由Matriptase-2介导的HAMP表达抑制,推测是通过抑制Matriptase-2裂解膜结合的HJV(血红素维林)的可能性来实现的。综上所述,本研究的结果已将HAI-2表征为Matriptase-2抑制剂,该抑制剂可调节hepcidin的合成,并为铁均位调节机制提供新见解,对治疗铁超负荷疾病具有重要的临床意义。

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