RGD Reference Report - TRPM2 activation by cyclic ADP-ribose at body temperature is involved in insulin secretion. - Rat Genome Database
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TRPM2 activation by cyclic ADP-ribose at body temperature is involved in insulin secretion.

Authors: Togashi, K  Hara, Y  Tominaga, T  Higashi, T  Konishi, Y  Mori, Y  Tominaga, M 
Citation: Togashi K, etal., EMBO J. 2006 May 3;25(9):1804-15. Epub 2006 Apr 6.
RGD ID: 9999436
Pubmed: (View Article at PubMed) PMID:16601673
DOI: Full-text: DOI:10.1038/sj.emboj.7601083

There are eight thermosensitive TRP (transient receptor potential) channels in mammals, and there might be other TRP channels sensitive to temperature stimuli. Here, we demonstrate that TRPM2 can be activated by exposure to warm temperatures (>35 degrees C) apparently via direct heat-evoked channel gating. beta-NAD(+)- or ADP-ribose-evoked TRPM2 activity is robustly potentiated at elevated temperatures. We also show that, even though cyclic ADP-ribose (cADPR) does not activate TRPM2 at 25 degrees C, co-application of heat and intracellular cADPR dramatically potentiates TRPM2 activity. Heat and cADPR evoke similar responses in rat insulinoma RIN-5F cells, which express TRPM2 endogenously. In pancreatic islets, TRPM2 is coexpressed with insulin, and mild heating of these cells evokes increases in both cytosolic Ca(2+) and insulin release, which is K(ATP) channel-independent and protein kinase A-mediated. Heat-evoked responses in both RIN-5F cells and pancreatic islets are significantly diminished by treatment with TRPM2-specific siRNA. These results identify TRPM2 as a potential molecular target for cADPR, and suggest that TRPM2 regulates Ca(2+) entry into pancreatic beta-cells at body temperature depending on the production of cADPR-related molecules, thereby regulating insulin secretion.


Gene Ontology Annotations    

Biological Process

Objects Annotated

Genes (Rattus norvegicus)
Trpm2  (transient receptor potential cation channel, subfamily M, member 2)

Additional Information