TY - CHAP
T1 - Methods for evaluation of vascular endothelial cell function with transient receptor potential (TRP) channel drugs
AU - Tjong, Yung Wui
AU - Yao, Xiaoqiang
N1 - Publisher Copyright:
© Springer Science+Business Media, LLC 2018.
PY - 2018
Y1 - 2018
N2 - Vascular endothelial transient potential (TRP) channels, located mostly on the plasma membrane of cells, are critical in regulatory and pathophysiological circumstances. The objective of this chapter is to describe several well-established approaches, ranging from function to molecular assays, to investigate the mechanistic role of TRP channels in vascular endothelial cells. We show experimental procedures and representative figures on the following methods: (1) Isolation and culture of vascular endothelial cells, (2) examination of electrophysiological activity of TRP channel by patch-clamping with whole-cell configuration and its function in vascular tone and blood flow by isometric tension and isobaric diameter measurements, and Laser Doppler flowmetry, (3) detection of TRP channel-mediated intracellular Ca2+ imaging by using fluorescent microscopy, and (4) determination of TRP channel interaction by coimmunoprecipitation, double immunofluorescence staining and Förster resonance energy transfer (FRET) detection.
AB - Vascular endothelial transient potential (TRP) channels, located mostly on the plasma membrane of cells, are critical in regulatory and pathophysiological circumstances. The objective of this chapter is to describe several well-established approaches, ranging from function to molecular assays, to investigate the mechanistic role of TRP channels in vascular endothelial cells. We show experimental procedures and representative figures on the following methods: (1) Isolation and culture of vascular endothelial cells, (2) examination of electrophysiological activity of TRP channel by patch-clamping with whole-cell configuration and its function in vascular tone and blood flow by isometric tension and isobaric diameter measurements, and Laser Doppler flowmetry, (3) detection of TRP channel-mediated intracellular Ca2+ imaging by using fluorescent microscopy, and (4) determination of TRP channel interaction by coimmunoprecipitation, double immunofluorescence staining and Förster resonance energy transfer (FRET) detection.
KW - Electrophysiology
KW - Intracellular calcium concentration
KW - Protein interaction
KW - Transient receptor potential channel
KW - Vascular endothelial cell
UR - http://www.scopus.com/inward/record.url?scp=85038885254&partnerID=8YFLogxK
U2 - 10.1007/978-1-4939-7553-2_13
DO - 10.1007/978-1-4939-7553-2_13
M3 - Chapter
C2 - 29264807
AN - SCOPUS:85038885254
T3 - Methods in Molecular Biology
SP - 195
EP - 210
BT - Methods in Molecular Biology
ER -