Regulation of electrogenic Na+/HCO3- cotransporter 1 (NBCe1) function and its dependence on m-TOR mediated phosphorylation of Ser245

Astrocytes are pivotal responders to alterations of extracellular pH, primarily by regulation of their principal acid-base transporter, the membrane-bound electrogenic Na+/bicarbonate cotransporter 1 (NBCe1). Here, we describe amammalian target of rapamycin (mTOR)-dependent and NBCe1-mediated astroglial response to extracellular acidosis. Using primary mouse cortical astrocytes, we investigated the effect of long-term extracellular metabolic acidosis on regulation of NBCe1 and elucidated the underlying molecular mechanisms by immunoblotting, biotinylation of surface proteins, intracellular H+ recording using the H+-sensitive dye 2 ',7 '-bis-(carboxyethyl)-5-(and-6)-carboxyfluorescein, and phosphoproteomic analysis. The results showed significant increase of NBCe1-mediated recovery of intracellular pH from acidification in WT astrocytes, but not in cortical astrocytes from NBCe1-deficient mice. Acidosis-induced upregulation of NBCe1 activity was prevented following inhibition of mTOR signaling by rapamycin. Yet, during acidosis or following exposure of astrocytes to rapamycin, surface protein abundance of NBCe1 remained -unchanged. Mutational analysis in HeLa cells suggested that NBCe1 activity was dependent on phosphorylation state of Ser(245), a residue conserved in all NBCe1 variants. Moreover, phosphorylation state of Ser(245) is regulated by mTOR and is inversely correlated with NBCe1 transport activity. Our results identify pSer(245) as a novel regulator of NBCe1 functional expression. We propose that context-dependent and mTOR-mediated multisite phosphorylation of serine residues of NBCe1 is likely to be a potent mechanism contributing to the response of astrocytes to acid/base challenges during pathophysiological conditions.

Automated summary

Astrocytes play a crucial role in responding to extracellular pH changes through the regulation of NBCe1, an acid-base transporter. The study found that mTOR-dependent and NBCe1-mediated astrocytic response to extracellular acidosis involves multiple molecular mechanisms, including serine residue phosphorylation at Ser(245) as a novel regulator of NBCe1 functional expression. The results suggest that context-dependent and mTOR-mediated multisite phosphorylation of serine residues of NBCe1 may be a potent mechanism contributing to astrocytes' response to acid/base challenges in pathophysiological conditions.