Key result
Acid loading in vivo and low pH in culture increased proximal tubule AT1 receptor cell surface expression and enhanced the ammoniagenic response to ANG II.
Acid challenges enhance the ammoniagenic response of the proximal tubule to ANG II partly by increasing AT1 receptor cell surface expression.
The proximal tubule defends the body against acid challenges by enhancing its production and secretion of ammonia. Our previous studies demonstrated an enhanced ammoniagenic response of the proximal tubule to ANG II added to the lumen in vitro after an in vivo acid challenge. The present study examined the effect of NH(4)Cl acid loading in vivo on renal cortical type 1 ANG II (AT(1)) receptor expression, the effect of low pH on AT(1) receptor expression in a proximal tubule cells in culture, and their response to ANG II. A short-term (18 h) NH(4)Cl load in vivo resulted in increased renal cortical AT(1) receptor mRNA expression and increased brush-border membrane AT(1) receptor protein expression levels. Changing the cell culture pH from 7.4 to 7.0 for at least 2 h increased cell surface expression of AT(1) receptors and enhanced the stimulatory effect of ANG II on ammonia production rates. This increased ammoniagenic response to ANG II and the early enhancement of cell surface expression induced by exposure of the cultured proximal tubule cells to pH 7.0 were prevented by treatment with colchicine. These results suggest that, after acid challenges, the enhanced ammoniagenic response of the proximal tubule to ANG II is, in part, mediated by increased AT(1) receptor cell surface expression and that the enhancement of receptor expression plays an important role in the early response of the proximal tubule to acid challenges.
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Nagami et al. (2008) studied this question. NH(4)Cl acid loading in vivo and low pH (7.0) in culture vs. Normal pH (7.4) / no acid load was evaluated on Renal cortical type 1 ANG II (AT1) receptor expression and ammoniagenic response to ANG II. Acid loading in vivo and low pH in culture increased proximal tubule AT1 receptor cell surface expression and enhanced the ammoniagenic response to ANG II.
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