Koster H P, van Os C H, Bindels R J
Department of Physiology, University of Nijmegen, The Netherlands.
Kidney Int. 1993 Apr;43(4):828-36. doi: 10.1038/ki.1993.117.
The presence of a Na(+)-Ca2+ exchange system has been previously demonstrated at the basolateral side of the cortical collecting system. The role of such an exchanger in maintaining low intracellular [Ca2+] ([Ca2+]i) in this nephron segment is now investigated. Cells from the connecting tubule and cortical collecting duct of rabbit kidneys were isolated by immunodissection with mAb R2G9 and subsequently cultured on glass coverslips. [Ca2+]i was measured in single cells using quantitative fluorescence microscopy. Surprisingly, isoosmotic substitution of extracellular Na+ ([Na+]o) for N-methylglucamine generated [Ca2+]i oscillations in individual cells instead of an anticipated sustained increase in [Ca2+]i. The amplitude of these oscillations ranged between 150 to 600 nM (average 308 +/- 19 nM) and occurred at a frequency of 0.63 +/- 0.03 min-1, with a duration of 44 +/- 2 seconds per spike. Oscillations were only observed in response to [Na+]o less than 5 mM and lasted until Na+o was re-introduced. The compound U73122 (10 microM), a new phospholipase C inhibitor, inhibited [Ca2+]i oscillations, which strongly suggests that IP3 generation initiates [Ca2+]i oscillations. [Ca2+]i oscillations were independent of extracellular Ca2+ and could not be inhibited by lanthanum ions, indicative for an intracellular source for the generation of Ca2+ spikes. Addition of thapsigargin, a specific inhibitor of endoplasmic reticulum Ca(2+)-ATPase activity, induced a considerable intracellular Ca2+ release, after which [Ca2+]i oscillations could no longer be provoked. Caffeine (20 mM) reversibly inhibited the Ca2+ oscillations, which implies that Ca(2+)-induced Ca2+ release is involved in generating these oscillations.(ABSTRACT TRUNCATED AT 250 WORDS)
