TY - JOUR
T1 - Kvα1 channels in murine arterioles
T2 - differential cellular expression and regulation of diameter
AU - Cheong, A.
AU - Dedman, A. M.
AU - Xu, S. Z.
AU - Beech, D. J.
PY - 2001/9/1
Y1 - 2001/9/1
N2 - The primary objectives of this study were to reveal cell-specific expression patterns and functions of voltage-gated K+ channel (Kvαl) subunits in precapillary arterioles of the murine cerebral circulation. Kvαl were detected using peptide-specific antibodies in immunofluorescence and Western blotting assays. Kvl.2 was localized almost exclusively to endothelial cells, whereas Kvl.5 was discretely localized to the nerves and nerve terminals that innervate the arterioles. Kvl.5 also localized specifically to arteriolar nerves in human pial membrane. Kvl.5 was notable for its absence from smooth muscle cells. Kv1.3, Kvl.4, and Kvl.6 were localized to endothelial and smooth muscle cells, although Kv1.4 had a low expression level. Kvl.1 was not expressed. Therefore, we show that different cell types of pial arterioles have distinct physiological expression profiles of Kvαl, conferring the possibility of differential modulation by extracellular and second messengers. Furthermore, we show recombinant agitoxin-2 and margatoxin are potent vasoconstrictors, suggesting that Kvαl subunits have a major function in determining arteriolar resistance to blood flow.
AB - The primary objectives of this study were to reveal cell-specific expression patterns and functions of voltage-gated K+ channel (Kvαl) subunits in precapillary arterioles of the murine cerebral circulation. Kvαl were detected using peptide-specific antibodies in immunofluorescence and Western blotting assays. Kvl.2 was localized almost exclusively to endothelial cells, whereas Kvl.5 was discretely localized to the nerves and nerve terminals that innervate the arterioles. Kvl.5 also localized specifically to arteriolar nerves in human pial membrane. Kvl.5 was notable for its absence from smooth muscle cells. Kv1.3, Kvl.4, and Kvl.6 were localized to endothelial and smooth muscle cells, although Kv1.4 had a low expression level. Kvl.1 was not expressed. Therefore, we show that different cell types of pial arterioles have distinct physiological expression profiles of Kvαl, conferring the possibility of differential modulation by extracellular and second messengers. Furthermore, we show recombinant agitoxin-2 and margatoxin are potent vasoconstrictors, suggesting that Kvαl subunits have a major function in determining arteriolar resistance to blood flow.
KW - Cerebral circulation
KW - Endothelium
KW - K channel
KW - Mouse
KW - Smooth muscle
KW - Vascular nerves
UR - http://www.scopus.com/inward/record.url?scp=0034834911&partnerID=8YFLogxK
UR - https://journals.physiology.org/doi/full/10.1152/ajpheart.2001.281.3.H1057
U2 - 10.1152/ajpheart.2001.281.3.h1057
DO - 10.1152/ajpheart.2001.281.3.h1057
M3 - Article
C2 - 11514271
AN - SCOPUS:0034834911
SN - 0363-6135
VL - 281
SP - H1057-H1065
JO - American Journal of Physiology - Heart and Circulatory Physiology
JF - American Journal of Physiology - Heart and Circulatory Physiology
IS - 3
ER -