| First Author | Giannaki M | Year | 2022 |
| Journal | J Cell Physiol | Volume | 237 |
| Issue | 2 | Pages | 1372-1388 |
| PubMed ID | 34642952 | Mgi Jnum | J:354606 |
| Mgi Id | MGI:7660901 | Doi | 10.1002/jcp.30601 |
| Citation | Giannaki M, et al. (2022) Regulation of electrogenic Na(+) /HCO(3)(-) cotransporter 1 (NBCe1) function and its dependence on m-TOR mediated phosphorylation of Ser(245). J Cell Physiol 237(2):1372-1388 |
| abstractText | 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. |
