Summary of ssbd-repos-000253

SSBD:database
URL

Name
ssbd-repos-000253 (253-Shimauchi-CalciumIonDyn)
URL
DOI
-

Title
Time courses images of Ca2+ responses in the TRPC inhibitor-expressing HEK293 cells or HeLa cells.
Description
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Submited Date
-
Release Date
2022-11-30
Updated Date
-
License
Funding information
-
File formats
Data size
575.5 MB

Organism
Homo sapiens
Strain
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Cell Line
HeLa cell, HEK293
Genes
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Proteins
TRPC3, TRPC3 inhibitors, TRPC6, TRPC7

GO Molecular Function (MF)
-
GO Biological Process (BP)
response to calcium ion
GO Cellular Component (CC)
-
Study Type
-
Imaging Methods
fluorescence microscopy

Method Summary
-
Related paper(s)

Tsukasa Shimauchi, Takuro Numaga-Tomita, Yuri Kato, Hiroyuki Morimoto, Kosuke Sakata, Ryosuke Matsukane, Akiyuki Nishimura, Kazuhiro Nishiyama, Atsushi Shibuta, Yutoku Horiuchi, Hitoshi Kurose, Sang Geon Kim, Yasuteru Urano, Takashi Ohshima, Motohiro Nishida (2022) A TRPC3/6 Channel Inhibitor Promotes Arteriogenesis after Hind-Limb Ischemia., Cells, Volume 11, Number 13

Published in 2022 Jun 27 (Electronic publication in June 27, 2022, midnight )

(Abstract) Retarded revascularization after progressive occlusion of large conductance arteries is a major cause of bad prognosis for peripheral artery disease (PAD). However, pharmacological treatment for PAD is still limited. We previously reported that suppression of transient receptor potential canonical (TRPC) 6 channel activity in vascular smooth muscle cells (VSMCs) facilitates VSMC differentiation without affecting proliferation and migration. In this study, we found that 1-benzilpiperadine derivative (1-BP), a selective inhibitor for TRPC3 and TRPC6 channel activities, induced VSMC differentiation. 1-BP-treated mice showed increased capillary arterialization and improvement of peripheral circulation and skeletal muscle mass after hind-limb ischemia (HLI) in mice. 1-BP had no additive effect on the facilitation of blood flow recovery after HLI in TRPC6-deficient mice, suggesting that suppression of TRPC6 underlies facilitation of the blood flow recovery by 1-BP. 1-BP also improved vascular nitric oxide bioavailability and blood flow recovery after HLI in hypercholesterolemic mice with endothelial dysfunction, suggesting the retrograde interaction from VSMCs to endothelium. These results suggest that 1-BP becomes a potential seed for PAD treatments that target vascular TRPC6 channels.
(MeSH Terms)

Contact(s)
Motohiro Nishida
Organization(s)
Kyushu University , Graduate School of Pharmaceutical Sciences
Image Data Contributors
Quantitative Data Contributors

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