Tumor necrosis factor-alpha, sphingomyelinase, and ceramide inhibit store-operated calcium entry in thyroid FRTL-5 cells

Citation
K. Tornquist et al., Tumor necrosis factor-alpha, sphingomyelinase, and ceramide inhibit store-operated calcium entry in thyroid FRTL-5 cells, J BIOL CHEM, 274(14), 1999, pp. 9370-9377
Citations number
62
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF BIOLOGICAL CHEMISTRY
ISSN journal
00219258 → ACNP
Volume
274
Issue
14
Year of publication
1999
Pages
9370 - 9377
Database
ISI
SICI code
0021-9258(19990402)274:14<9370:TNFSAC>2.0.ZU;2-X
Abstract
Tumor necrosis factor alpha (TNF-alpha) is a potent inhibitor of proliferat ion in several cell types, including thyroid FRTL-5 cells. As intracellular free calcium ([Ca2+](i)) is a major signal in activating proliferation, we investigated the effect of TNF-alpha on calcium fluxes in FRTL-5 cells, TN F-alpha per se did not modulate resting [Ca2+](i). However, preincubation ( 10 min) of the cells with 1-100 ng/ml TNF-alpha decreased the thapsigargin (Tg)-evoked store-operated calcium entry in a concentration-dependent manne r. TNF-alpha did not inhibit the mobilization of sequestered calcium, To in vestigate whether the effect of TNF-alpha on calcium entry was mediated via the sphingomyelinase pathway, the cells were pretreated with sphingomyelin ase (SMase) prior to stimulation with Tg. SMase inhibited the Tg-evoked cal cium entry in a concentration-dependent manner. Furthermore, an inhibition of calcium entry was obtained after preincubation of the cells with the mem brane-permeable C-2-ceramide and C-6-ceramide analogues, The inactive ceram ides dihydro-C-2 and dihydro-C-6 showed only marginal effects, Neither SMas e, C-2-ceramide, nor C-6-ceramide affected the release of sequestered calci um. C-2- and C-6-ceramide also decreased the ATP-evoked calcium entry, with out affecting the release of sequestered calcium. The effect of TNF-alpha a nd SMase was inhibited by the kinase inhibitor staurosporin and by the prot ein kinase C (PKC) inhibitor calphostin C but not by down-regulation of PKC . However, Ive were unable to measure a significant activation of PKC using TNF-alpha or C-6-ceramide, The effect of TNF-alpha was not mediated via ac tivation of either c-Sun N-terminal kinase or p38 kinase, We were unable to detect an increase in the ceramide (or sphingosine) content of the cells a fter stimulation with TNF-alpha for up to 30 min, Thus, one mechanism of ac tion of TNF-alpha; SMase, and ceramide on thyroid FRTL-5 cells is to inhibi t calcium entry.