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Mitogenic signaling by Gq/11-coupled receptors

机译:Gq / 11耦合受体的有丝分裂信号。

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摘要

By binding to their cognate GPCRs, many potent mitogens such as neuropeptides, angiotensin II or lysophosphatidic acid stimulate cell proliferation via engaging the ERK/MAPK cascade. As mentioned before, agonists stimulating Gq/11-coupled receptors activate PLCb isoforms thereby activating PKCs and elevating [Ca2+]i. These two second messengers represent key molecules for coupling Gq/11 proteins to the ERK/MAPK cascade. In this work, by means of GnRH in gonadotropic aT3-1 cells and galanin or bradykinin in SCLC cells, different aspects of Gq/11-dependent mitogenic signaling pathways were revealed. Our findings together with previous reports underline the notion that signaling pathways emanating from Gq/11-coupled receptors are tightly regulated in a cell- and receptor-specific manner.
机译:通过结合其同源的GPCR,许多有效的促有丝分裂原,例如神经肽,血管紧张素II或溶血磷脂酸,通过参与ERK / MAPK级联反应来刺激细胞增殖。如前所述,刺激Gq / 11偶联受体的激动剂激活PLCb亚型,从而激活PKCs并升高[Ca2 +] i。这两个第二信使代表了将Gq / 11蛋白偶联到ERK / MAPK级联反应的关键分子。在这项工作中,借助于促性腺激素aT3-1细胞中的GnRH和SCLC细胞中的甘丙肽或缓激肽,揭示了Gq / 11依赖性有丝分裂信号通路的不同方面。我们的发现以及以前的报道强调了这样一种观念,即以细胞和受体特异性方式严格调控Gq / 11偶联受体发出的信号通路。

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