Suppr超能文献

mAKAP信号体与心肌细胞肥大

The mAKAP signalosome and cardiac myocyte hypertrophy.

作者信息

Bauman Andrea L, Michel Jennifer J Carlisle, Henson Edward, Dodge-Kafka Kimberly L, Kapiloff Michael S

机构信息

Department of Pediatrics, Heart Research Center, Oregon Health & Science University, Portland, Oregon 97239, USA.

出版信息

IUBMB Life. 2007 Mar;59(3):163-9. doi: 10.1080/15216540701358593.

Abstract

Cardiac hypertrophy is regulated by a large intracellular signal transduction network. Each of the many signaling pathways in this network contributes uniquely to the control of cell growth. In the last few years, it has become apparent that multimolecular signaling complexes or 'signalosomes' are important for mediating crosstalk between different signaling pathways. These complexes integrate upstream signals and control downstream effectors. In the cardiac myocyte, the protein mAKAPbeta serves as a scaffold for a large signalosome that is responsive to upstream cAMP, Ca(2+), and mitogen-activated protein kinase signaling. The mAKAPbeta signalosome is important for the control of NFATc transcription factor activity and for the overall induction of myocyte hypertrophy.

摘要

心脏肥大受一个庞大的细胞内信号转导网络调控。该网络中的众多信号通路各自独特地参与细胞生长的控制。在过去几年中,多分子信号复合物或“信号体”对于介导不同信号通路之间的相互作用变得愈发明显。这些复合物整合上游信号并控制下游效应器。在心肌细胞中,蛋白质mAKAPβ作为一个大型信号体的支架,该信号体对上游环磷酸腺苷(cAMP)、钙离子(Ca²⁺)和丝裂原活化蛋白激酶信号有反应。mAKAPβ信号体对于控制活化T细胞核因子c(NFATc)转录因子活性以及对心肌细胞肥大的整体诱导很重要。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验