Two Transient Receptor Potential Channels at Focal Adhesions.

IF 1.9 4区 生物学 Q4 CELL BIOLOGY
Journal of Histochemistry & Cytochemistry Pub Date : 2023-09-01 Epub Date: 2023-08-18 DOI:10.1369/00221554231194119
Ioli Mitsou, Cathrine Rein Carlson, Hinke A B Multhaupt, Cord Brakebusch, John R Couchman
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引用次数: 0

Abstract

Recently there have been reports that identify two transient receptor potential channels in cell-matrix junctions known as focal adhesions. These are the calcium channel TRP canonical 7 and the calcium-activated monovalent ion channel, TRP melastatin (TRPM) 4. Here, we report on the occurrence of TRPM4 in focal adhesions of fibroblasts. Of three commercial antibodies recognizing this channel, only one yielded focal adhesion staining, while the other two did not. The epitope recognized by the focal adhesion-localizing antibody was mapped to the extreme C-terminus of the TRPM4 protein. The other two antibodies bind to N-terminal regions of the TRPM4 proteins. Deletion of the TRPM4 gene by CRISPR/cas9 techniques confirmed that this channel is a bona fide focal adhesion component, while expression of full-length TRPM4 proteins suggested that processing may occur to yield a form that localizes to focal adhesions. Given the reports that this channel may influence migratory behavior of cells and is linked to cardiovascular disease, TRPM4 functions in adhesion should be explored in greater depth. (J Histochem Cytochem 71: 495-508, 2023).

局灶性粘连处的两个瞬时受体电位通道。
最近有报道称,在细胞基质连接中发现了两种称为局灶性粘连的瞬时受体电位通道。这些是钙通道TRP规范7和钙活化的单价离子通道TRP美司他丁(TRPM)4。在此,我们报道了TRPM4在成纤维细胞局灶性粘连中的发生。在识别该通道的三种商业抗体中,只有一种产生了局灶性粘附染色,而其他两种没有。粘附定位抗体识别的表位被定位到TRPM4蛋白的末端C末端。另外两种抗体与TRPM4蛋白的N-末端区域结合。CRISPR/cas9技术对TRPM4基因的缺失证实了该通道是真正的局灶性粘附成分,而全长TRPM4蛋白的表达表明,可能发生加工以产生定位于局灶性粘连的形式。鉴于有报道称该通道可能影响细胞的迁移行为,并与心血管疾病有关,TRPM4在粘附中的功能应得到更深入的探索。(J Histochem Cytochem 71:495-5082023)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.00
自引率
0.00%
发文量
32
审稿时长
1 months
期刊介绍: Journal of Histochemistry & Cytochemistry (JHC) has been a pre-eminent cell biology journal for over 50 years. Published monthly, JHC offers primary research articles, timely reviews, editorials, and perspectives on the structure and function of cells, tissues, and organs, as well as mechanisms of development, differentiation, and disease. JHC also publishes new developments in microscopy and imaging, especially where imaging techniques complement current genetic, molecular and biochemical investigations of cell and tissue function. JHC offers generous space for articles and recognizing the value of images that reveal molecular, cellular and tissue organization, offers free color to all authors.
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