Receptor Biology Lab, University of Antwerp, 2610 Wilrijk, Belgium.
Department of Chemistry, Middle East Technical University, Çankaya, Ankara 06800, Turkey.
Int J Mol Sci. 2021 Dec 13;22(24):13387. doi: 10.3390/ijms222413387.
GPCRs arguably represent the most effective current therapeutic targets for a plethora of diseases. GPCRs also possess a pivotal role in the regulation of the physiological balance between healthy and pathological conditions; thus, their importance in systems biology cannot be underestimated. The molecular diversity of GPCR signaling systems is likely to be closely associated with disease-associated changes in organismal tissue complexity and compartmentalization, thus enabling a nuanced GPCR-based capacity to interdict multiple disease pathomechanisms at a systemic level. GPCRs have been long considered as controllers of communication between tissues and cells. This communication involves the ligand-mediated control of cell surface receptors that then direct their stimuli to impact cell physiology. Given the tremendous success of GPCRs as therapeutic targets, considerable focus has been placed on the ability of these therapeutics to modulate diseases by acting at cell surface receptors. In the past decade, however, attention has focused upon how stable multiprotein GPCR superstructures, termed receptorsomes, both at the cell surface membrane and in the intracellular domain dictate and condition long-term GPCR activities associated with the regulation of protein expression patterns, cellular stress responses and DNA integrity management. The ability of these receptorsomes (often in the absence of typical cell surface ligands) to control complex cellular activities implicates them as key controllers of the functional balance between health and disease. A greater understanding of this function of GPCRs is likely to significantly augment our ability to further employ these proteins in a multitude of diseases.
G 蛋白偶联受体 (GPCRs) 可以说是目前针对多种疾病最有效的治疗靶点。GPCRs 在健康和病理条件下的生理平衡调节中也起着关键作用;因此,它们在系统生物学中的重要性不容低估。GPCR 信号系统的分子多样性很可能与与疾病相关的组织复杂性和区室化变化密切相关,从而使基于 GPCR 的能力能够在系统水平上阻断多种疾病发病机制。GPCRs 一直被认为是组织和细胞之间通讯的控制器。这种通讯涉及配体介导的细胞表面受体控制,然后将其刺激物引导至影响细胞生理学。鉴于 GPCR 作为治疗靶点的巨大成功,人们相当关注这些治疗药物通过作用于细胞表面受体来调节疾病的能力。然而,在过去十年中,人们的注意力集中在稳定的多蛋白 GPCR 超结构(称为受体复合物)上,这些超结构存在于细胞膜表面和细胞内结构域,决定和调节与蛋白质表达模式、细胞应激反应和 DNA 完整性管理相关的长期 GPCR 活性。这些受体复合物(通常在没有典型细胞表面配体的情况下)控制复杂的细胞活动,这表明它们是健康和疾病之间功能平衡的关键控制器。对 GPCR 这一功能的更深入了解,很可能会显著提高我们在多种疾病中进一步利用这些蛋白质的能力。