NBCn1 (slc4a7) Mediates the Na+-Dependent Bicarbonate Transport Important for Regulation of Intracellular pH in Mouse Vascular Smooth Muscle Cells

The contribution of sodium-dependent bicarbonate transport to intracellular pH (pHi) regulation in vascular smooth muscle cells is controversial, partly because the molecular identity of the transporter(s) responsible has not been identified. Here, using the pH-sensitive fluorophore 2′,7′-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF), we show that smooth muscle cells of intact mouse mesenteric, coronary, and cerebral small arteries all display a sodium- and bicarbonate-dependent pHi recovery after an NH4+-prepulse. The sodium-dependent bicarbonate flux was largely 4,4′-diisothiocyanatostilbene-2,2′-disulphonic acid (DIDS) sensitive (56% to 91%) and of a magnitude similar to the amiloride-sensitive flux. Additionally, steady-state pHi was lower (0.2 to 0.4 pH units magnitude) in all 3 vascular beds when CO2/bicarbonate was omitted. RT-PCR analyses showed that NBCn1 (slc4a7) is the only Na+-dependent bicarbonate transporter of the slc4 family detectable at the mRNA level in all 3 vascular beds investigated. Whole-mount immunolabeling and immunogold electron microscopy confirmed the presence of NBCn1 protein in the sarcolemma of mouse mesenteric small arterial smooth muscle cells. Intact mouse mesenteric small arteries were electropermeated to facilitate transfection with small interfering RNA targeting NBCn1, which resulted in an approximate 43% decrease in the ratio of NBCn1 to glyceraldehyde-3-phosphate dehydrogenase mRNA. After knock-down, we found a decreased steady-state pHi (0.21±0.08 pH units) as well as a 68±10% decrease in the net Na+-dependent, amiloride-insensitive base influx after acid load. Finally, omission of CO2/bicarbonate resulted in a decreased contractile response to norepinephrine after sustained exposure to the agonist, underlining the importance of CO2/bicarbonate for vascular contractility. We conclude that NBCn1 mediates the Na+-dependent bicarbonate transport important for pHi regulation in smooth muscle cells of mouse mesenteric, coronary, and cerebral small arteries.

[1]  S. Nielsen,et al.  An anti-NH2-terminal antibody localizes NBCn1 to heart endothelia and skeletal and vascular smooth muscle cells. , 2006, American journal of physiology. Heart and circulatory physiology.

[2]  W. Boron,et al.  Na+-dependent HCO3- uptake into the rat choroid plexus epithelium is partially DIDS sensitive. , 2005, American journal of physiology. Cell physiology.

[3]  F. Di Sole,et al.  Na+/H+ exchangers: physiology and link to hypertension and organ ischemia , 2005, Current opinion in nephrology and hypertension.

[4]  L. Fliegel The Na+/H+ exchanger isoform 1. , 2005, The international journal of biochemistry & cell biology.

[5]  S. Nielsen,et al.  Basolateral Na+‐dependent HCO3− transporter NBCn1‐mediated HCO3− influx in rat medullary thick ascending limb , 2004, The Journal of physiology.

[6]  M. Wiederholt,et al.  Evidence for Na/H exchange and Cl/HCO3 exchange in A10 vascular smooth muscle cells , 1988, Pflügers Archiv.

[7]  M. Romero,et al.  The SLC4 family of HCO 3 - transporters. , 2004, Pflugers Archiv : European journal of physiology.

[8]  M. Romero,et al.  The SLC4 family of HCO3− transporters , 2004, Pflügers Archiv.

[9]  Jianping Wu,et al.  Hypercapnic Acidosis Activates KATP Channels in Vascular Smooth Muscles , 2003, Circulation research.

[10]  Min Goo Lee,et al.  The Cystic Fibrosis Transmembrane Conductance Regulator Interacts with and Regulates the Activity of the HCO 3 − Salvage Transporter Human Na+-HCO 3 − Cotransport Isoform 3* , 2002, The Journal of Biological Chemistry.

[11]  R. Schubert,et al.  Protons Inhibit the BKCa Channel of Rat Small Artery Smooth Muscle Cells , 2001, Journal of Vascular Research.

[12]  R. Schubert,et al.  Protons inhibit the BK(Ca) channel of rat small artery smooth muscle cells. , 2001, Journal of vascular research.

[13]  David A. Dean,et al.  Gene Transfer to Intact Mesenteric Arteries by Electroporation , 2000, Journal of Vascular Research.

[14]  A. Harper,et al.  The three mechanisms of intracellular chloride accumulation in vascular smooth muscle of human umbilical and placental arteries , 2000, Pflügers Archiv.

[15]  W. Boron,et al.  An electroneutral sodium/bicarbonate cotransporter NBCn1 and associated sodium channel , 2000, Nature.

[16]  D. Newman,et al.  Cloning, Tissue Distribution, Genomic Organization, and Functional Characterization of NBC3, a New Member of the Sodium Bicarbonate Cotransporter Family* , 1999, The Journal of Biological Chemistry.

[17]  R. Vaughan-Jones,et al.  Characterization of intracellular pH regulation in the guinea‐pig ventricular myocyte , 1999, The Journal of physiology.

[18]  J. LaManna,et al.  Identification and expression of the Na+/H+ exchanger in mammalian cerebrovascular and choroidal tissues: characterization by amiloride-sensitive [3H]MIA binding and RT-PCR analysis. , 1998, Brain research. Molecular brain research.

[19]  Godfrey L. Smith,et al.  A review of the actions and control of intracellular pH in vascular smooth muscle. , 1998, Cardiovascular research.

[20]  S. Wray,et al.  The role of the sarcolemmal Ca2+ ‐ATPase in the pH transients associated with contraction in rat smooth muscle , 1997, The Journal of physiology.

[21]  D. Yannoukakos,et al.  AE anion exchanger mRNA and protein expression in vascular smooth muscle cells, aorta, and renal microvessels. , 1997, American journal of physiology. Renal physiology.

[22]  W. Boron,et al.  Motor responses of cultured rat cerebral vascular smooth muscle cells to intra- and extracellular pH changes. , 1997, The American journal of physiology.

[23]  N. Lassen,et al.  Role of extracellular and intracellular acidosis for hypercapnia-induced inhibition of tension of isolated rat cerebral arteries. , 1995, Circulation research.

[24]  C. Aickin Regulation of intracellular pH in smooth muscle cells of the guinea‐pig femoral artery. , 1994, The Journal of physiology.

[25]  C. Seidel,et al.  Effects of pHi on Na(+)-H+, Na(+)-dependent, and Na(+)-independent C1(-)-HCO3-exchangers in vascular smooth muscle. , 1991, The American journal of physiology.

[26]  A. Hughes,et al.  Chloride and bicarbonate transport in rat resistance arteries. , 1991, The Journal of physiology.

[27]  P. Little,et al.  Intracellular pH in human arterial smooth muscle. Regulation by Na+/H+ exchange and a novel 5-(N-ethyl-N-isopropyl)amiloride-sensitive Na(+)- and HCO3(-)-dependent mechanism. , 1990, Circulation research.

[28]  Intracellular-pH dependence of Na-H exchange and acid loading in quiescent and arginine vasopressin-activated mesangial cells. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[29]  E. Cragoe,et al.  Na(+)-H+ and Na(+)-dependent Cl(-)-HCO3- exchange control pHi in vascular smooth muscle. , 1990, The American journal of physiology.

[30]  R. Putnam,et al.  Steady-state pHi, buffering power, and effect of CO2 in a smooth muscle-like cell line. , 1990, The American journal of physiology.

[31]  R. Alexander,et al.  Spontaneously hypertensive rat vascular smooth muscle cells in culture exhibit increased growth and Na+/H+ exchange. , 1989, The Journal of clinical investigation.

[32]  M. Lazdunski,et al.  Dual control of the intracellular pH in aortic smooth muscle cells by a cAMP-sensitive HCO3-/Cl- antiporter and a protein kinase C-sensitive Na+/H+ antiporter. , 1988, The Journal of biological chemistry.

[33]  C. Aalkjaer,et al.  Intracellular pH regulation in resting and contracting segments of rat mesenteric resistance vessels. , 1988, The Journal of physiology.

[34]  C. Aalkjaer,et al.  Effect of changes in intracellular pH on the contractility of rat resistance vessels. , 1988, Progress in biochemical pharmacology.

[35]  H. Lodish,et al.  Primary structure and transmembrane orientation of the murine anion exchange protein , 1985, Nature.

[36]  W. Boron,et al.  Intracellular pH. , 1981, Physiological reviews.

[37]  M. Mulvany,et al.  Contractile properties of small arterial resistance vessels in spontaneously hypertensive and normotensive rats. , 1977, Circulation research.