Inhibition of Na + /H + exchanger enhances low pH-induced L-selectin shedding and β 2 -integrin surface expression in human neutrophils

• Published in: American Journal of Physiology: Cell Physiology 2008-11, Vol.295 (5), p.C1454-C1463
• Main Authors: Kaba, Nubia K., Schultz, Joanne, Law, Foon-Yee, Lefort, Craig T., Martel-Gallegos, Guadalupe, Kim, Minsoo, Waugh, Richard E., Arreola, Jorge, Knauf, Philip A.
• Format: Article
• Language: English
• ISSN: 0363-6143; 1522-1563
• DOI: 10.1152/ajpcell.00535.2007

Ischemia-reperfusion injury is a common pathological occurrence causing tissue damage in heart attack and stroke. Entrapment of neutrophils in the vasculature during ischemic events has been implicated in this process. In this study, we examine the effects that lactacidosis and consequent reductions in intracellular pH (pH i ) have on surface expression of adhesion molecules on neutrophils. When human neutrophils were exposed to pH 6 lactate, there was a marked decrease in surface L-selectin (CD62L) levels, and the decrease was significantly enhanced by inclusion of Na + /H + exchanger (NHE) inhibitor 5-( N, N-hexamethylene)amiloride (HMA). Similar effects were observed when pH i was reduced while maintaining normal extracellular pH, by using an NH 4 Cl prepulse followed by washes and incubation in pH 7.4 buffer containing NHE inhibitors [HMA, cariporide, or 5-( N, N-dimethyl)amiloride (DMA)]. The amount of L-selectin shedding induced by different concentrations of NH 4 Cl in the prepulse correlated with the level of intracellular acidification with an apparent p K of 6.3. In contrast, β 2 -integrin (CD11b and CD18) was only slightly upregulated in the low-pH i condition and was enhanced by NHE inhibition to a much lesser extent. L-selectin shedding was prevented by treating human neutrophils with inhibitors of extracellular metalloproteases (RO-31-9790 and KD-IX-73-4) or with inhibitors of intracellular signaling via p38 MAP kinase (SB-203580 and SB-239063), implying a transmembrane effect of pH i . Taken together, these data suggest that the ability of NHE inhibitors such as HMA to reduce ischemia-reperfusion injury may be related to the nearly complete removal of L-selectin from the neutrophil surface.