Zeng Xianqin, Zhu Liping, Xiao Rui, Liu Bingxun, Sun Mengxiang, Liu Fangbo, Hao Qiang, Lu Yankai, Zhang Jiwei, Li Jiansha, Wang Tao, Wei Xiang, Hu Qinghua
From the Department of Pathophysiology, School of Basic Medicine (X.Z., L.Z., R.X., B.L., M.S., F.L., Q. Hao, Q. Hu), Key Laboratory of Pulmonary Diseases of Ministry of Health (X.Z., L.Z., R.X., B.L., M.S., F.L., Q. Hao, Y.L., J.Z., J.L., T.W., Q. Hu), Department of Pathology, Tongji Hospital (Y.L., J.L.), Department of Pathology, Union Hospital (J.Z.), Department of Respiratory and Critical Care Medicine (T.W.), and Department of Cardiothoracic and Vascular Surgery, Tongji Hospital (X.W.), Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China.
Hypertension. 2017 May;69(5):844-854. doi: 10.1161/HYPERTENSIONAHA.116.08743. Epub 2017 Mar 27.
Hypoxia-induced mitogenic factor (HIMF) is an inflammatory cytokine playing important role(s) in the development of hypoxic pulmonary hypertension. The molecular target mediating HIMF-stimulated downstream events remains unclear. The coimmunoprecipitation screen identified extracellular calcium-sensing receptor (CaSR) as the binding partner for HIMF in pulmonary artery smooth muscle cells. The yeast 2-hybrid assay then revealed the binding of HIMF to the intracellular, not the extracellular, domain of extracellular CaSR. The binding of HIMF enhanced the activity of extracellular CaSR and mediated hypoxia-evoked proliferation of pulmonary artery smooth cells and the development of pulmonary vascular remodeling and pulmonary hypertension, all of which was specifically attenuated by a synthesized membrane-permeable peptide flanking the core amino acids of the intracellular binding domain of extracellular CaSR. Thus, HIMF induces pulmonary hypertension as a nonclassical ligand of extracellular CaSR, and the binding motif of extracellular CaSR can be therapeutically exploitable.
缺氧诱导有丝分裂因子(HIMF)是一种炎症细胞因子,在缺氧性肺动脉高压的发展中起重要作用。介导HIMF刺激的下游事件的分子靶点仍不清楚。免疫共沉淀筛选确定细胞外钙敏感受体(CaSR)是肺动脉平滑肌细胞中HIMF的结合伴侣。酵母双杂交试验随后揭示HIMF与细胞外CaSR的细胞内而非细胞外结构域结合。HIMF的结合增强了细胞外CaSR的活性,并介导了缺氧诱发的肺动脉平滑肌细胞增殖以及肺血管重塑和肺动脉高压的发展,而所有这些都被一种合成的、位于细胞外CaSR细胞内结合结构域核心氨基酸侧翼的膜通透性肽特异性减弱。因此,HIMF作为细胞外CaSR的非经典配体诱导肺动脉高压,并且细胞外CaSR 的结合基序可用于治疗。