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通过受体串扰实现 PAR 信号转导的多样化。

Diversification of PAR signaling through receptor crosstalk.

机构信息

Department of Molecular Neuropathology, Instituto de Fisiología Celular, UNAM, Apartado Postal 70-253, Ciudad Universitaria, Mexico City, CdMx, Mexico.

出版信息

Cell Mol Biol Lett. 2022 Sep 10;27(1):77. doi: 10.1186/s11658-022-00382-0.

Abstract

Protease activated receptors (PARs) are among the first receptors shown to transactivate other receptors: noticeably, these interactions are not limited to members of the same family, but involve receptors as diverse as receptor kinases, prostanoid receptors, purinergic receptors and ionic channels among others. In this review, we will focus on the evidence for PAR interactions with members of their own family, as well as with other types of receptors. We will discuss recent evidence as well as what we consider as emerging areas to explore; from the signalling pathways triggered, to the physiological and pathological relevance of these interactions, since this additional level of molecular cross-talk between receptors and signaling pathways is only beginning to be explored and represents a novel mechanism providing diversity to receptor function and play important roles in physiology and disease.

摘要

蛋白酶激活受体(PARs)是最早被证明能转激活其他受体的受体之一:值得注意的是,这些相互作用不仅限于同一家族的成员,还涉及受体激酶、前列腺素受体、嘌呤能受体和离子通道等多种受体。在这篇综述中,我们将重点介绍 PAR 与自身家族成员以及其他类型受体相互作用的证据。我们将讨论最近的证据以及我们认为正在出现的探索领域;从触发的信号通路到这些相互作用的生理和病理相关性,因为受体和信号通路之间这种额外的分子串扰水平才刚刚开始被探索,这代表了一种提供受体功能多样性的新机制,并在生理和疾病中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f30/9463773/2c9080b6ffd3/11658_2022_382_Fig1_HTML.jpg

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