By David H. Ingbar, Joseph M. Lasnier (auth.), Sadis Matalon, Jacob Lasha Sznajder (eds.)
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4). , <:> 20 U C~ :J '= = t ::'" :c. '" -< I ~ oi Z t50 13 1 1 ~~~ . / ~ tOO 50 0 * " I I ~ *..! ,- and Figure 4. Effect of hypo xia and rcoxygcnation on mRNA expres sion of subunits in ATll ce lls. 6. 12 or 18 h. 0 2). At the end of ex posure. RNase protection assays we re perfo rmed on ccl i lysates (RNA equivale nt to (() 6 cells). K ATPase mRNA levels we re quant itated using an Instant Image r. Data were norma lized for the co rrespo nding ac tin sig nal in each lane. K- A TPase subunit mRNA I actin mRNA.
Triphosphate (AIP), one of the cellular effectors known to modulate Na,K-ATPase activity 32, may be severely decreased during hypoxiaf' . In our experiments however, ATP content was reduced by 40% only in ATIl cells exposed for 3 h to 0% 02 (Table 3). Such a moderate ATP depletion is likely not responsible for OsRb influx decrease inasmuch as we previously reported 34 that a 90% ATP depletion was not sufficient to impair Na,K-ATPase activity in normoxic ATIl cells. Intracellular Na concentration also modulates Na,KATPase activity in intact cells.
Cell. Physiol . 157:544-554 (1993). 20. S. Suzuki. T. Sakuma, M. Sugita, Y. Hoshikawa, M. Noda, S. Ono. T. Tanita, and S. '1 111. J. Resp ir. Crit. Care Me d . 153:A505 Abstr. (1996). 21. C. Planes. G. Friedlander. A. Loiseau. C. Amiel, and C. Clerici. Inhibition of Na,K-ATPase activity after prolonged hypoxia in an alveolar epithelial cell line, AIII. J. Phy siol . 271:L71-L78 (1996). 22. B. E. Goodman, F. Fleisher, and E. D. Crandall, Evidence for active ion transport by cultured monolayers of pulmonary alveolar epithelial cells.