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The Roles of Rasd1 small G proteins and leptin in the activation of TRPC4 transient receptor potential channels

Authors
Wie, JinhongKim, Byung JooMyeong, JongyunHa, KotdajiJeong, Seung JooYang, DongkiKim, EuiyongJeon, Ju-HongSo, Insuk
Issue Date
4-Jul-2015
Publisher
TAYLOR & FRANCIS INC
Citation
CHANNELS, v.9, no.4, pp.186 - 195
Journal Title
CHANNELS
Volume
9
Number
4
Start Page
186
End Page
195
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/10318
DOI
10.1080/19336950.2015.1058454
ISSN
1933-6950
Abstract
TRPC4 is important regulators of electrical excitability in gastrointestinal myocytes, pancreatic -cells and neurons. Much is known regarding the assembly and function of these channels including TRPC1 as a homotetramer or a heteromultimer and the roles that their interacting proteins play in controlling these events. Further, they are one of the best-studied targets of G protein-coupled receptors and growth factors in general and G(i/o) and G(q) protein coupled receptor or epidermal growth factor and leptin in particular. However, our understanding of the roles of small G proteins and leptin on TRPC4 channels is still rudimentary. We discuss potential roles for Rasd1 small G protein and leptin in channel activation in addition to their known role in cellular signaling.
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