Fibrosis after organ damage leads to organ structural damage and functional decline. Fibrosis is characterized by the activation of fibroblasts and the secretion of type I collagen-based extracellular matrix, but the mechanism remains to be explored. CRTH2, the prostaglandin D2 receptor, mainly mediates the activation of Th2 cells, and its role in fibrosis is not clear. We found that CRTH2 interacts with LARP6 in the endoplasmic reticulum, and CRTH2 deficiency results in a significant increase in types I and III collagen synthesis both in vivo and in vitro. LARP6 affects collagen synthesis through increase typeⅠ and Ⅲ collagen mRNA stability, so we hypothesize that CRTH2 interact with LARP6 on the endoplasmic reticulum to reduce the stability of collagen mRNA and regulate the homeostasis of collagen synthesis. We will investigate the role of CRTH2 in multiple organ fibrosis models using CRTH2 KO mice; explore the interaction of CRTH2 with LARP6 on the endoplasmic reticulum by molecular biology experiments; verify the role of CRTH2 in the regulation of fibrosis progression using LARP6 KO mice. This study aims to reveal the role and mechanism of CRTH2 in organ fibrosis and provide a new target for the treatment of fibrosis-related diseases.
机体器官损伤后的纤维化导致器官结构破坏和功能衰退。纤维化以成纤维细胞活化并分泌以Ⅰ型胶原为主的细胞外基质为特点,但机制仍需探究。前列腺素D2受体CRTH2,主要介导Th2细胞的活化,其在纤维化中的作用并不清楚。我们发现CRTH2和LARP6在内质网上相互作用;无论是体内还是体外, CRTH2缺失都导致Ⅰ和Ⅲ型胶原合成明显增加。LARP6增加Ⅰ和Ⅲ型胶原mRNA稳定性而影响胶原蛋白合成,因此推测CRTH2在内质网上与LARP6相互作用降低胶原mRNA稳定性,调节胶原合成的稳态平衡。我们将利用CRTH2 KO小鼠探讨CRTH2在多个器官纤维化模型中的作用;通过分子生物学手段探究CRTH2与LARP6在内质网上的互作方式;利用LARP6 KO小鼠验证CRTH2在调控器官纤维化进程中的作用。该研究旨在揭示CRTH2在器官纤维化中的作用及机制,为纤维化相关疾病治疗提供新的靶点。
器官纤维化以胶原蛋白为主的细胞外基质的过度沉积为标志,纤维化可能导致器官结构改变和功能障碍。然而调节器官纤维化中胶原生物合成的分子机制尚不清楚。在本项目中,我们发现在成纤维细胞中,经典的前列腺素D2的细胞质膜受体CRTH2(chemoattractant receptor homologous molecule expressed on TH2 cells ),以Caveolin-1依赖的方式转运到内质网膜上。内质网上锚定的CRTH2结合LARP6(La ribonucleoprotein domain family member 6)的胶原mRNA识别基序,促进细胞中胶原mRNA的降解。CRTH2特异性缺失会增加成纤维细胞中的胶原蛋白合成,并加剧小鼠的损伤诱导的器官纤维化,而LARP6的抑制可以挽救这一情况。我们合成了CRTH2氨基端小肽,该小肽与LARP6结合减少胶原的产生。进一步地,基于LARP6与CRTH2的结合位点,我们筛选出了布美他尼,布美他尼可结合LARP6 mRNA识别基序,抑制胶原的生物合成,并减轻博莱霉素诱导的小鼠肺纤维化。总之,本项目的发现揭示内质网膜上的CRTH2与LARP6相互作用具有一种新的抗纤维化功能,这可能是治疗纤维化疾病的一个有效靶点。
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数据更新时间:2023-05-31
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