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细胞肿胀增强配体驱动的β-肾上腺素能信号。

Cell swelling enhances ligand-driven β-adrenergic signaling.

机构信息

Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.

School of Physics and Astronomy, University of St Andrews, St Andrews, UK.

出版信息

Nat Commun. 2024 Sep 7;15(1):7822. doi: 10.1038/s41467-024-52191-y.

Abstract

G protein-coupled receptors' conformational landscape can be affected by their local, microscopic interactions within the cell plasma membrane. We employ here a pleiotropic stimulus, namely osmotic swelling, to alter the cortical environment within intact cells and monitor the response in terms of receptor function and downstream signaling. We observe that in osmotically swollen cells the β2-adrenergic receptor, a prototypical GPCR, favors an active conformation, resulting in cAMP transient responses to adrenergic stimulation that have increased amplitude. The results are validated in primary cell types such as adult cardiomyocytes, a model system where swelling occurs upon ischemia-reperfusion injury. Our results suggest that receptors' function is finely modulated by their biophysical context, and specifically that osmotic swelling acts as a potentiator of downstream signaling, not only for the β2-adrenergic receptor, but also for other receptors, hinting at a more general regulatory mechanism.

摘要

G 蛋白偶联受体的构象景观可能受到其在细胞质膜内的局部微观相互作用的影响。在这里,我们使用一种多效刺激物,即渗透压膨胀,来改变完整细胞内的皮质环境,并根据受体功能和下游信号监测反应。我们观察到,在渗透压膨胀的细胞中,β2-肾上腺素能受体(一种典型的 GPCR)有利于一种活跃的构象,导致肾上腺素刺激引起的 cAMP 瞬态反应的幅度增加。这些结果在原代细胞类型中得到了验证,如成年心肌细胞,在这种模型系统中,细胞在缺血再灌注损伤时会发生肿胀。我们的结果表明,受体的功能受到其生物物理环境的精细调节,具体来说,渗透压膨胀作为下游信号的增强剂起作用,不仅对β2-肾上腺素能受体,而且对其他受体也是如此,这暗示着一种更普遍的调节机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee72/11379887/6e8f7aa86cc4/41467_2024_52191_Fig1_HTML.jpg

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