Sorbonne Université, INSERM, CNRS, Institut de la Vision, 17 rue Moreau, 75012 Paris, France.
CNRS, ESPCI-Paris, PSL Research University, Brain Plasticity Unit, UMR 8249, 10 rue Vauquelin, 75005 Paris, France.
Cell Rep. 2019 Jun 25;27(13):4003-4012.e6. doi: 10.1016/j.celrep.2019.05.102.
cGMP is critical to a variety of cellular processes, but the available tools to interfere with endogenous cGMP lack cellular and subcellular specificity. We introduce SponGee, a genetically encoded chelator of this cyclic nucleotide that enables in vitro and in vivo manipulations in single cells and in biochemically defined subcellular compartments. SponGee buffers physiological changes in cGMP concentration in various model systems while not affecting cAMP signals. We provide proof-of-concept strategies by using this tool to highlight the role of cGMP signaling in vivo and in discrete subcellular domains. SponGee enables the investigation of local cGMP signals in vivo and paves the way for therapeutic strategies that prevent downstream signaling activation.
cGMP 对多种细胞过程至关重要,但现有的干扰内源性 cGMP 的工具缺乏细胞和亚细胞特异性。我们引入了 SponGee,这是一种基因编码的该环核苷酸螯合剂,可在单细胞和生物化学定义的亚细胞隔室中进行体外和体内操作。SponGee 缓冲了各种模型系统中 cGMP 浓度的生理变化,而不影响 cAMP 信号。我们提供了使用该工具的概念验证策略,以突出 cGMP 信号在体内和离散亚细胞结构域中的作用。SponGee 使体内局部 cGMP 信号的研究成为可能,并为防止下游信号激活的治疗策略铺平了道路。