https://scholars.lib.ntu.edu.tw/handle/123456789/519119
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Wu K.-C. | en_US |
dc.contributor.author | HORNG-HUEI LIOU | en_US |
dc.contributor.author | Kao Y.-H. | en_US |
dc.contributor.author | Lee C.-Y. | en_US |
dc.contributor.author | CHUN-JUNG LIN | en_US |
dc.creator | Wu K.-C.;Horng-Huei Liou;Kao Y.-H.;Lee C.-Y.;Lin C.-J. | - |
dc.date.accessioned | 2020-11-03T09:53:18Z | - |
dc.date.available | 2020-11-03T09:53:18Z | - |
dc.date.issued | 2017 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019044959&doi=10.1016%2fj.nbd.2017.05.001&partnerID=40&md5=3682e0836111a34b7d7b2fc0c3a91263 | - |
dc.identifier.uri | https://scholars.lib.ntu.edu.tw/handle/123456789/519119 | - |
dc.description.abstract | Oligomeric α-synuclein is a key mediator in the pathogenesis of Parkinson's disease (PD) and is mainly cleared by autophagy-lysosomal pathway, whose dysfunction results in the accumulation and cell-to-cell transmission of α-synuclein. In this study, concomitant with the accumulation of iron and oligomeric α-synuclein, higher expression of a lysosomal iron transporter, natural resistance-associated macrophage protein-1 (Nramp1), was observed in microglia in post-mortem striatum of sporadic PD patients. Using Nramp1-deficient macrophage (RAW264.7) and microglial (BV-2) cells as in-vitro models, iron exposure significantly reduced the degradation rate of the administered human α-synuclein oligomers, which can be restored by the expression of the wild-type, but not mutant (D543N), Nramp1. Likewise, under iron overload condition, mice with functional Nramp1 (DBA/2 and C57BL/6 congenic mice carrying functional Nramp1) had a better ability to degrade infused human α-synuclein oligomers than mice with nonfunctional Nramp1 (C57BL/6) in the brain and microglia. The interplay between iron and Nramp1 exhibited parallel effects on the clearance of α-synuclein and the activity of lysosomal cathepsin D in vitro and in vivo. Collectively, these findings suggest that the function of Nramp1 contributes to microglial degradation of oligomeric α-synuclein under iron overload condition and may be implicated in the pathogenesis of PD. ? 2017 Elsevier Inc. | - |
dc.publisher | Academic Press Inc. | - |
dc.relation.ispartof | Neurobiology of Disease | - |
dc.subject.classification | [SDGs]SDG3 | - |
dc.subject.other | alpha synuclein; cathepsin D; natural resistance associated macrophage protein 1; oligomer; AIF1 protein, human; alpha synuclein; ammonium ferric sulfate; cathepsin D; cation transport protein; DNA binding protein; ferric ion; glial fibrillary acidic protein; lysosome associated membrane protein 1; natural resistance-associated macrophage protein 1; TUBB3 protein, human; tubulin; animal cell; animal experiment; animal tissue; Article; brain tissue; C57BL 6 mouse; controlled study; corpus striatum; exposure; extraction; genetic transfection; human; human cell; human tissue; immunofluorescence; immunohistochemistry; in vitro study; in vivo study; iron overload; male; microglia; mouse; mutant; nonhuman; Parkinson disease; pathogenesis; priority journal; protein degradation; protein expression; RAW 264.7 cell line; Western blotting; wild type; aged; analysis of variance; animal; C57BL mouse; case control study; drug effects; female; genetics; metabolism; microglia; Parkinson disease; pathology; site directed mutagenesis; transformed cell line; transgenic mouse; very elderly; Aged; Aged, 80 and over; alpha-Synuclein; Analysis of Variance; Animals; Case-Control Studies; Cathepsin D; Cation Transport Proteins; Cell Line, Transformed; Corpus Striatum; DNA-Binding Proteins; Female; Ferric Compounds; Glial Fibrillary Acidic Protein; Humans; Lysosomal-Associated Membrane Protein 1; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microglia; Mutagenesis, Site-Directed; Parkinson Disease; Transfection; Tubulin | - |
dc.title | The critical role of Nramp1 in degrading α-synuclein oligomers in microglia under iron overload condition | en_US |
dc.type | journal article | en |
dc.identifier.doi | 10.1016/j.nbd.2017.05.001 | - |
dc.identifier.pmid | 28476637 | - |
dc.identifier.scopus | 2-s2.0-85019044959 | - |
dc.relation.pages | 61-72 | - |
dc.relation.journalvolume | 104 | - |
item.fulltext | no fulltext | - |
item.cerifentitytype | Publications | - |
item.openairetype | journal article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_6501 | - |
item.grantfulltext | none | - |
crisitem.author.dept | National Taiwan University Hospital Yun-Lin Branch | - |
crisitem.author.dept | Neurology | - |
crisitem.author.dept | Pharmacology | - |
crisitem.author.dept | Brain and Mind Sciences | - |
crisitem.author.dept | Neurology-NTUH | - |
crisitem.author.dept | Pharmacy | - |
crisitem.author.dept | School of Pharmacy | - |
crisitem.author.orcid | 0000-0001-6537-5346 | - |
crisitem.author.orcid | 0000-0001-9220-3507 | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | College of Medicine | - |
顯示於: | 醫學系 |
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