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Understanding CELSRs - Cadherin EGF LAG seven-pass G-type receptors

机译:了解CELSRs-钙黏着蛋白EGF LAG七遍G型受体

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摘要

The cadherin EGF LAG seven-pass G-type receptors (CELSRs) are a special subgroup of adhesion G protein-coupled receptors (GPCRs), which are pivotal regulators of many biological processes such as neuronal/endocrine cell differentiation, vessel valve formation and the control of planar cell polarity during embryonic development. All three members of the CELSR family (CELSR1-3) have large ecto-domains that form homophilic interactions and encompass more than 2,000 amino acids. Mutations in the ecto-domain or other gene locations of CELSRs are associated with neural tube defects (NTDs) and other diseases in humans. Celsr knockout (KO) animals have many developmental defects. Therefore, specific agonists or antagonists of CELSR members may have therapeutic potential. Although significant progress has been made regarding the functions and biochemical properties of CELSRs, our knowledge of these receptors is still lacking, especially considering that they are broadly distributed but have few characterized functions in a limited number of tissues. The dynamic activation and inactivation of CELSRs and the presence of endogenous ligands beyond homophilic interactions remain elusive, as do the regulatory mechanisms and downstream signaling of these receptors. Given this motivation, future studies with more advanced cell biology or biochemical tools, such as conditional KO mice, may provide further insights into the mechanisms underlying CELSR function, laying the foundation for the design of new CELSR-targeted therapeutic reagents.
机译:钙黏着蛋白EGF LAG七遍G型受体(CELSRs)是粘附G蛋白偶联受体(GPCR)的一个特殊亚组,它是许多生物学过程(如神经元/内分泌细胞分化,血管瓣膜形成和神经胶质形成的关键调节器)。在胚胎发育过程中控制平面细胞极性。 CELSR家族的所有三个成员(CELSR1-3)都具有大的胞外域,这些域形成同源相互作用,并包含2000多个氨基酸。 CELSRs的胞外域或其他基因位置的突变与人类的神经管缺陷(NTD)和其他疾病有关。 Celsr基因敲除(KO)动物具有许多发育缺陷。因此,CELSR成员的特异性激动剂或拮抗剂可能具有治疗潜力。尽管在CELSRs的功能和生化特性方面已取得重大进展,但我们仍然缺乏对这些受体的了解,特别是考虑到它们分布广泛,但在有限的组织中几乎没有特征性的功能。 CELSRs的动态激活和失活以及同质相互作用之外的内源性配体的存在仍然难以捉摸,这些受体的调节机制和下游信号传导也难以捉摸。有了这种动力,未来使用更高级的细胞生物学或生化工具(例如条件KO小鼠)进行的研究可能会进一步了解CELSR功能的潜在机制,为设计靶向CELSR的新型治疗试剂奠定基础。

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