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Am J Physiol Endocrinol Metab (January 15, 2002). doi:10.1152/ajpendo.00176.2001
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Articles in PresS, published online ahead of print January 15, 2002
Am J Physiol Endocrinol Metab, 10.1152/ajpendo.00176.2001
Submitted on April 23, 2001
Accepted on December 20, 2001

Hypo-osmotic shock stimulates insulin secretion by two distinct mechanisms. Studies with the ßHC9 cell

Susanne G Straub1, Samira Daniel1, and Geoffrey W Sharp1*

1 Molecular Medicine, Cornell University, Ithaca, NY, USA

* To whom correspondence should be addressed. E-mail: gws2{at}cornell.edu.

Exposure of ßHC9 cells to a Krebs-Ringer bicarbonate Hepes buffer (KRBH) made hypotonic by a reduction of 25 mM NaCl resulted in a prompt stimulation of insulin release. The stimulation was transient and release rates returned to basal levels after 10 minutes. The response resembles that of the first phase of glucose-stimulated insulin release. The response did not occur if the reduction in NaCl was compensated for by the addition of an equivalent osmolar amount of sorbitol, so the stimulation of release is due to the osmolarity change and not the reduction in NaCl. The hypo-osmotic shock released insulin in KRBH made up with or without Ca2+. The L-type Ca2+ channel blocker nitrendipine inhibited the response in normal KRBH but had no effect in KRBH made up without Ca2+ despite the fact that the latter response was larger than in the presence of extracellular Ca2+. Similar data were obtained with calciseptine, which also blocks L-type channels. The T-type Ca2+ channel blocker flunarizine was without effect as also was the chloride channel blocker DIDS. In parallel studies, the readily releasable pool of insulin-containing granules was monitored. Immunoprecipitation of the t-SNARE protein syntaxin and co-immunoprecipitation of the v-SNARE VAMP-2 was used as an indicator of the readily releasable granule pool. After hypotonic shock in the presence of extracellular Ca2+, the amount of VAMP-2 that was co-immunoprecipitated by antibodies against syntaxin was much reduced compared to controls. Therefore, under these conditions hypotonic shock stimulates exocytosis of the readily releasable pool of insulin-containing granules. No such reduction was seen in the absence of extracellular Ca2+. In conclusion, having re-examined the effect of hypo-osmotic shock on insulin secretion in the presence and absence of Ca2+ (with EGTA in the medium), it is clear that two different mechanisms are operative under these conditions. Additionally, these two mechanisms may be associated with the release of two distinct pools of insulin-containing granules.




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