Developmental Endocrinology Unit, Hormone and Molecular Genetics Laboratory (LIM/42), Hospital das Clinicas, Sao Paulo University Medical School, São Paulo 05403-900, Brazil.
Sci Signal. 2010 Oct 12;3(143):re7. doi: 10.1126/scisignal.3143re7.
G protein-coupled receptors (GPCRs) constitute a large family of cell membrane receptors that affect embryogenesis, development, and child physiology, and they are targets for approved drugs and those still in development. The sensitivity of GPCRs to their respective extracellular hormones, neurotransmitters, and environmental stimulants, as well as their interaction with other receptors and intracellular signaling proteins (such as receptor activity-modifying proteins), contribute to variations in child development, growth, and maturation. Here, we summarize current knowledge about the mechanisms of activation (in either the presence or absence of ligands) that lead to the sensitivities of GPCRs and their respective effects as seen throughout human developmental and maturational phases.
G 蛋白偶联受体(GPCRs)是细胞膜受体的一个大家族,它们影响胚胎发生、发育和儿童生理,是已批准药物和仍在开发中的药物的靶点。GPCR 对各自的细胞外激素、神经递质和环境刺激物的敏感性,以及它们与其他受体和细胞内信号蛋白(如受体活性修饰蛋白)的相互作用,导致儿童发育、生长和成熟的差异。在这里,我们总结了目前关于激活机制(有或没有配体)的知识,这些机制导致了 GPCR 的敏感性及其在整个人类发育和成熟阶段的各自影响。