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10.1016/j.bbamcr.2016.05.003 http://scihub22266oqcxt.onion/10.1016/j.bbamcr.2016.05.003 27157538!ä!27157538 Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27157538&cmd=llinks): Failed to open stream: HTTP request failed! 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Altered expression of Mg(2+) transport proteins during Parkinson s disease-like dopaminergic cell degeneration in PC12 cells |pdf=|usr=}}{{27157538}} gab.com Text Altered expression of Mg(2+) transport proteins during Parkinson s disease-like dopaminergic cell degeneration in PC12 cells JO: Biochim Biophys Acta http://www.kidney.de/pget.php?&tw=1&pmid=27157538 #FOAvip Mg(2+) is an essential cation to maintain cellular functions, and intracellular Mg(2+) concentration ([Mg(2+)]i) is regulated by Mg(2+) channels and transporters. In our previous study, we demonstrated that MPP(+) elicits Mg(2+) influx across the cell membrane and Mg(2+) mobilization from mitochondria, and the resulting [Mg(2+)]i is an important determinants of the cell viability in MPP(+) model of Parkinson's disease (PD). It indicates that cellular Mg(2+) transport is one of the important factors to determine the progress of PD. However, whether the expression levels of Mg(2+) transport proteins change in the progress of PD has still been obscure. In this study, we estimated the mRNA expression levels of Mg(2+) transport proteins upon the exposure to MPP(+). In thirteen Mg(2+) transport proteins examined, mRNA expression level of SLC41A2 was increased and that of ACDP2, NIPA1 and MMgT2 were decreased. Knockdown of SLC41A2, ACDP2 or NIPA1 accelerated the MPP(+)-induced cell degeneration, and overexpression attenuated it. The decrease in the mRNA expression levels of NIPA1 and MMgT2 were also elicited by rotenone, H2O2 and FCCP, indicating that mitochondrial dysfunction related to this down-regulation. The increase in that of SLC41A2 was induced by an uncoupler, FCCP, as well as MPP(+), suggesting that it is an intrinsic protection mechanism against depolarized mitochondrial membrane potential and/or cellular ATP depletion. Our results shown here indicate that alteration of Mg(2+) transport proteins is implicated in the MPP(+) model of PD, and it affects cell degeneration. Twit Text FOAVip Altered expression of Mg(2+) transport proteins during Parkinson s disease-like dopaminergic cell degeneration in PC12 cells ????Biochim Biophys Acta http://www.kidney.de/pget.php?&tw=1&pmid=27157538 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27157538 #FOAvip English Wikipedia <ref>{{Cite pmid|27157538}}</ref> Altered expression of Mg(2+) transport proteins during Parkinson s disease-like dopaminergic cell degeneration in PC12 cells #MMPMID27157538 Shindo Y; Yamanaka R; Suzuki K; Hotta K; Oka K Biochim Biophys Acta 2016[Aug]; 1863 (8): 1979-84 PMID27157538show ga Mg(2+) is an essential cation to maintain cellular functions, and intracellular Mg(2+) concentration ([Mg(2+)]i) is regulated by Mg(2+) channels and transporters. In our previous study, we demonstrated that MPP(+) elicits Mg(2+) influx across the cell membrane and Mg(2+) mobilization from mitochondria, and the resulting [Mg(2+)]i is an important determinants of the cell viability in MPP(+) model of Parkinson's disease (PD). It indicates that cellular Mg(2+) transport is one of the important factors to determine the progress of PD. However, whether the expression levels of Mg(2+) transport proteins change in the progress of PD has still been obscure. In this study, we estimated the mRNA expression levels of Mg(2+) transport proteins upon the exposure to MPP(+). In thirteen Mg(2+) transport proteins examined, mRNA expression level of SLC41A2 was increased and that of ACDP2, NIPA1 and MMgT2 were decreased. Knockdown of SLC41A2, ACDP2 or NIPA1 accelerated the MPP(+)-induced cell degeneration, and overexpression attenuated it. The decrease in the mRNA expression levels of NIPA1 and MMgT2 were also elicited by rotenone, H2O2 and FCCP, indicating that mitochondrial dysfunction related to this down-regulation. The increase in that of SLC41A2 was induced by an uncoupler, FCCP, as well as MPP(+), suggesting that it is an intrinsic protection mechanism against depolarized mitochondrial membrane potential and/or cellular ATP depletion. Our results shown here indicate that alteration of Mg(2+) transport proteins is implicated in the MPP(+) model of PD, and it affects cell degeneration. |1-Methyl-4-phenylpyridinium/pharmacology[MESH] |Adenosine Triphosphate/metabolism[MESH] |Animals[MESH] |Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone/pharmacology[MESH] |Cation Transport Proteins/*biosynthesis/genetics[MESH] |Cell Differentiation/drug effects[MESH] |Hydrogen Peroxide/pharmacology[MESH] |Ion Transport/drug effects[MESH] |MPTP Poisoning[MESH] |Magnesium/*metabolism[MESH] |Membrane Potential, Mitochondrial/drug effects/physiology[MESH] |Mitochondria/metabolism[MESH] |Nerve Degeneration[MESH] |Nerve Growth Factor/pharmacology[MESH] |PC12 Cells/*drug effects/metabolism[MESH] |RNA Interference[MESH] |RNA, Messenger/biosynthesis/genetics[MESH] |RNA, Small Interfering/genetics[MESH] |Rats[MESH]Altered expression of Mg(2+) transport proteins during Parkinson s dis(epmc).pdf DeepDyve Pubget Overpricing