Effects of Urotensin II on Intracellular pH regulation in Cultured Human Internal Mammary Artery Smooth Muscle Cells | Boulder Peptide Symposium

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Effects of Urotensin II on Intracellular pH regulation in Cultured Human Internal Mammary Artery Smooth Muscle Cells

Effects of Urotensin II on Intracellular pH regulation in Cultured Human Internal Mammary Artery Smooth Muscle Cells

Publication date: Available online 24 April 2014 Source:Peptides

Author(s): Yi-Ting Tsai , Chung-Yi Lee , Chih-Chin Hsu , Chung-Yi Chang , Ming-Kai Hsueh , Eagle Yi-Kung Huang , Chien-Sung Tsai , Shih-Hurng Loh

The Na+-H+ exchanger (NHE) and the Na+-HCO3 co-transporter (NBC) have been confirmed as two major active acid extruders in many mammalian cells. Whether the NHE and NBC functional co-exist in human internal mammary artery smooth muscle cells (HIMASMCs) remains unclear. The aims of the present study were to investigate the acid-extruding mechanisms and to explore the effects of urotensin-II (U-II), a powerful vasoconstrictor, on pHi regulators in HIMASMCs. We investigated the changes of pHi by BCECF-fluorescence in HIMASMCs. We found that (a) two Na+-dependent acid extruders, i.e. NHE and NBC, functionally co-exist; (b) U-II (3 ∼ 100nM) induced a concentration-dependent intracellular acidosis; and (c) U-II (3 ∼ 100nM) caused a concentration-dependent increase on NHE activity, while decrease on NBC activity. In summary, we demonstrate for the first time that two acid-extruders, NHE and NBC, functionally co-exist in HIMASMCs. Moreover, U-II induces a concentration-dependent intracellular acidosis through the balanced effect of its effect on increasing NHE activity and decreasing NBC activity

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