Effect of Lithium treatment on SOCE components in Chorea Acanthocytosis

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dc.contributor.advisor Ruth, Peter (Prof. Dr.)
dc.contributor.author Sukkar, Basma
dc.date.accessioned 2020-08-13T11:41:57Z
dc.date.available 2020-08-13T11:41:57Z
dc.date.issued 2020-08-13
dc.identifier.other 1728981018 de_DE
dc.identifier.uri http://hdl.handle.net/10900/104863
dc.identifier.uri http://nbn-resolving.de/urn:nbn:de:bsz:21-dspace-1048630 de_DE
dc.identifier.uri http://dx.doi.org/10.15496/publikation-46241
dc.description.abstract Chorea Acanthocytosis (ChAc) is an autosomal recessive neurodegenerative disease characterized by limb chorea, dystonia, epilepsy and acanthocytosis. The patients have a reduced life expectancy of only around 60 years. This disorder is caused by a loss-of-function mutation of the VPS13A (vacuolar protein sorting-associated protein A) gene, which is the encoding gene of chorein. Normally, chorein stimulates phosphoinositide 3-kinase (PI3K), which is involved in the regulation of Ca2+ influx. Oscillations of intracellular Ca2+ concentration regulate, among other cell components, proliferation, differentiation and apoptosis. Emptying of intracellular Ca2+ stores activates the Store-operated Ca2+ entry (SOCE), which leads to a conformational change and opening of the channel through the interaction between the Ca2+ concentration sensor protein, the Stromal Interacting Molecule 1 (STIM1), and the pore-forming channel, Orai1. The Ca2+ channel is known also as Ca2+ release-activated channel (CRAC). SOCE is increased by lithium via stimulation of serum & glucocorticoid-inducible kinase (SGK1), which is responsible in cells for stimulating the expression of Orai1 and STIM1 as well regulating the transcription factor: Nuclear Factor 'kappa-light-chain-enhancer' of activated B-cells (NFкB). Lithium is used in the treatment of bipolar disorders and can cross the blood-brain barrier (BBB). In this study, fibroblasts and neurons of ChAc patients have been shown to have decreased SOCE and an increased rate of apoptosis. Fibroblasts were isolated from six ChAc patients and six healthy donors. In addition, fibroblasts were obtained from three additional patients and healthy donors and induced pluripotent stem cells (iPSCs) were generated in order to differentiate them into neurons. Western blotting and calcium imaging showed a significant reduction in the amount of Orai1 protein and SOCE, respectively, in fibroblasts and iPSC-differentiated neurons of ChAc patients compared to healthy donors. RT-PCR showed a significant decrease in the mRNA levels of Orai1 and STIM1 in iPSC-differentiated neurons of ChAc patients. Apoptosis was detected by annexin-V / propidium iodide staining via flow cytometry and was in fibroblasts and iPSC-differentiated neurons of ChAc patients significantly higher than in those of healthy donors. In this study, it could be shown that the treatment of fibroblasts and neurons of ChAc patients with lithium positively influenced SOCE, an effect significantly reduced by the Orai1 blocker, 2-aminoethoxy diphenyl borate (2-APB). Lithium induced a significant decrease in apoptosis, an effect again abrogated by 2-APB. The mRNA and protein expression of Orai1 and STIM1 were increased by lithium, an effect reversed by inhibition of SGK1 and NFкB. In conclusion, the apoptotic effect of chorein deficiency in fibroblasts and neurons of ChAc patients is in part due to the decreased expression of Orai1, STIM1 and SOCE. Treatment with lithium could reverse this effect, via the SGK1/NFкB signaling pathway, which shows that lithium could be a new treatment for Chorea Acanthocytosis. en
dc.language.iso en de_DE
dc.publisher Universität Tübingen de_DE
dc.rights ubt-podno de_DE
dc.rights.uri http://tobias-lib.uni-tuebingen.de/doku/lic_ohne_pod.php?la=de de_DE
dc.rights.uri http://tobias-lib.uni-tuebingen.de/doku/lic_ohne_pod.php?la=en en
dc.subject.classification Lithium , Chorea , Calcium , Signaling , Nervenzelle , Apoptosis de_DE
dc.subject.ddc 500 de_DE
dc.subject.other Neurodegeneration en
dc.subject.other SOCE en
dc.subject.other Orai1 en
dc.subject.other NFκB en
dc.subject.other SGK1 en
dc.title Effect of Lithium treatment on SOCE components in Chorea Acanthocytosis en
dc.type PhDThesis de_DE
dcterms.dateAccepted 2020-02-06
utue.publikation.fachbereich Pharmazie de_DE
utue.publikation.fakultaet 7 Mathematisch-Naturwissenschaftliche Fakultät de_DE

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