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Inhibition of Lithium Sensitive Orai1/ STIM1 Expression and Store Operated Ca2+ Entry in Chorea-Acanthocytosis Neurons by NF-κB Inhibitor Wogonin.
- Source :
-
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology [Cell Physiol Biochem] 2018; Vol. 51 (1), pp. 278-289. Date of Electronic Publication: 2018 Nov 19. - Publication Year :
- 2018
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Abstract
- Background/aims: The neurodegenerative disease Chorea-Acanthocytosis (ChAc) is caused by loss-of-function-mutations of the chorein-encoding gene VPS13A. In ChAc neurons transcript levels and protein abundance of Ca2+ release activated channel moiety (CRAC) Orai1 as well as its regulator STIM1/2 are decreased, resulting in blunted store operated Ca2+-entry (SOCE) and enhanced suicidal cell death. SOCE is up-regulated and cell death decreased by lithium. The effects of lithium are paralleled by upregulation of serum & glucocorticoid inducible kinase SGK1 and abrogated by pharmacological SGK1 inhibition. In other cell types SGK1 has been shown to be partially effective by upregulation of NFκB, a transcription factor stimulating the expression of Orai1 and STIM. The present study explored whether pharmacological inhibition of NFκB interferes with Orai1/STIM1/2 expression and SOCE and their upregulation by lithium in ChAc neurons.<br />Methods: Cortical neurons were differentiated from induced pluripotent stem cells generated from fibroblasts of ChAc patients and healthy volunteers. Orai1 and STIM1 transcript levels and protein abundance were estimated from qRT-PCR and Western blotting, respectively, cytosolic Ca2+-activity ([Ca2+]i) from Fura-2-fluorescence, SOCE from increase of [Ca2+]i following Ca2+ re-addition after Ca2+-store depletion with sarco-endoplasmatic Ca2+-ATPase inhibitor thapsigargin (1µM), as well as CRAC current utilizing whole cell patch clamp recording.<br />Results: Orai1 and STIM1 transcript levels and protein abundance as well as SOCE and CRAC current were significantly enhanced by lithium treatment (2 mM, 24 hours). These effects were reversed by NFκB inhibitor wogonin (50 µM).<br />Conclusion: The stimulation of expression and function of Orai1/STIM1/2 by lithium in ChAc neurons are disrupted by pharmacological NFκB inhibition.<br /> (© 2018 The Author(s). Published by S. Karger AG, Basel.)
- Subjects :
- Calcium-Transporting ATPases antagonists & inhibitors
Calcium-Transporting ATPases metabolism
Cell Differentiation
Cells, Cultured
Humans
Induced Pluripotent Stem Cells cytology
Membrane Potentials drug effects
NF-kappa B antagonists & inhibitors
NF-kappa B metabolism
Neoplasm Proteins genetics
Neurodegenerative Diseases metabolism
Neurodegenerative Diseases pathology
Neurons cytology
Neurons drug effects
Neurons metabolism
ORAI1 Protein genetics
Patch-Clamp Techniques
Stromal Interaction Molecule 1 genetics
Thapsigargin pharmacology
Calcium metabolism
Flavanones pharmacology
Gene Expression drug effects
Lithium pharmacology
Neoplasm Proteins metabolism
ORAI1 Protein metabolism
Stromal Interaction Molecule 1 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1421-9778
- Volume :
- 51
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 30453283
- Full Text :
- https://doi.org/10.1159/000495229