American journal of physiology. Heart and circulatory physiology · 2001
K(V)alpha1 channels in murine arterioles: differential cellular expression and regulation of diameter.
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Cheong A, Dedman A M, Xu S Z, Beech D J
Аннотация
The primary objectives of this study were to reveal cell-specific expression patterns and functions of voltage-gated K(+) channel (K(V)alpha1) subunits in precapillary arterioles of the murine cerebral circulation. K(V)alpha1 were detected using peptide-specific antibodies in immunofluorescence and Western blotting assays. K(V)1.2 was localized almost exclusively to endothelial cells, whereas K(V)1.5 was discretely localized to the nerves and nerve terminals that innervate the arterioles. K(V)1.5 also localized specifically to arteriolar nerves in human pial membrane. K(V)1.5 was notable for its absence from smooth muscle cells. K(V)1.3, K(V)1.4, and K(V)1.6 were localized to endothelial and smooth muscle cells, although K(V)1.4 had a low expression level. K(V)1.1 was not expressed. Therefore, we show that different cell types of pial arterioles have distinct physiological expression profiles of K(V)alpha1, conferring the possibility of differential modulation by extracellular and second messengers. Furthermore, we show recombinant agitoxin-2 and margatoxin are potent vasoconstrictors, suggesting that K(V)alpha1 subunits have a major function in determining arteriolar resistance to blood flow.
Предметные рубрики MeSH
AnimalsArteriolesBlotting, WesternCerebral CortexCrotalid VenomsDelayed Rectifier Potassium ChannelsIn Vitro TechniquesKv1.1 Potassium ChannelKv1.2 Potassium ChannelKv1.3 Potassium ChannelKv1.4 Potassium ChannelKv1.5 Potassium ChannelMaleMiceMice, Inbred BALB CNeurotoxinsOrgan SpecificityPia MaterPotassium ChannelsPotassium Channels, Voltage-GatedRNA, MessengerRecombinant ProteinsScorpion VenomsSequence Homology, Amino AcidVascular Patency