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GABAB受体在人主动脉平滑肌细胞中表达,并调节细胞内钙离子浓度。

GABAB receptors are expressed in human aortic smooth muscle cells and regulate the intracellular Ca(2+) concentration.

作者信息

Wang Xu-Ping, Cheng Zhen-Ying, Schmid Katrina L

机构信息

The Key Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education and Chinese Ministry of Health, Qilu Hospital, Shandong University, Jinan, Shandong, China.

出版信息

Heart Vessels. 2015 Mar;30(2):249-57. doi: 10.1007/s00380-014-0499-2. Epub 2014 Mar 30.

Abstract

The aim of this study was to investigate the expression of GABAB receptors, a subclass of receptors to the inhibitory neurotransmitter gamma-aminobutyric acid (GABAB), in human aortic smooth muscle cells (HASMCs), and to explore if altering receptor activation modified intracellular Ca(2+) concentration ([Ca(2+)]i) of HASMCs. Real-time PCR, western blots and immunofluorescence were used to determine the expression of GABABR1 and GABABR2 in cultured HASMCs. Immunohistochemistry was used to localize the two subunits in human left anterior descending artery (LAD). The effects of the GABAB receptor agonist baclofen on [Ca(2+)]i in cultured HASMCs were demonstrated using fluo-3. Both GABABR1 and GABABR2 mRNA and protein were identified in cultured HASMCs and antibody staining was also localized to smooth muscle cells of human LAD. 100 μM baclofen caused a transient increase of [Ca(2+)]i in cultured HASMCs regardless of whether Ca(2+) was added to the medium, and the effects were inhibited by pre-treatment with CGP46381 (selective GABAB receptor antagonist), pertussis toxin (a Gi/o protein inhibitor), and U73122 (a phospholipase C blocker). GABAB receptors are expressed in HASMCs and regulate the [Ca(2+)]i via a Gi/o-coupled receptor pathway and a phospholipase C activation pathway.

摘要

本研究旨在调查抑制性神经递质γ-氨基丁酸(GABA)的受体亚类GABAB受体在人主动脉平滑肌细胞(HASMCs)中的表达,并探讨改变受体激活是否会改变HASMCs的细胞内钙离子浓度([Ca(2+)]i)。采用实时PCR、蛋白质免疫印迹和免疫荧光法测定培养的HASMCs中GABABR1和GABABR2的表达。采用免疫组织化学法在人左前降支动脉(LAD)中定位这两个亚基。使用fluo-3证明了GABAB受体激动剂巴氯芬对培养的HASMCs中[Ca(2+)]i的影响。在培养的HASMCs中鉴定出GABABR1和GABABR2的mRNA和蛋白质,抗体染色也定位于人LAD的平滑肌细胞。无论培养基中是否添加Ca(2+),100 μM巴氯芬都会导致培养的HASMCs中[Ca(2+)]i短暂升高,并且这些作用被CGP46381(选择性GABAB受体拮抗剂)、百日咳毒素(一种Gi/o蛋白抑制剂)和U73122(一种磷脂酶C阻滞剂)预处理所抑制。GABAB受体在HASMCs中表达,并通过Gi/o偶联受体途径和磷脂酶C激活途径调节[Ca(2+)]i。

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