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Mesencephalic astrocyte‐derived neurotrophic factor reduces cell apoptosis via upregulating GRP78 in SH‐SY5Y cells
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Citations
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References
2016
Year
Manf TreatmentApoptosisCell DeathSynaptic SignalingCellular PhysiologySocial SciencesOxidative StressNeuroinflammationDegenerative PathologyNeurologyCell SignalingGrp78 ExpressionsMolecular SignalingMolecular NeuroscienceBrain-immune InteractionNeuroprotectionSh‐sy5y CellsNeurotrophic Factor ReducesCell BiologyNeurodegenerative DiseasesDopaminergic NeuronsNeuroscienceMedicine
Mesencephalic astrocyte-derived neurotrophic factor (MANF) protects dopaminergic neurons from damage. In this study, we used MTT, immunohistochemistry, and TUNEL staining to investigate the protective effect of MANF in SH-SY5Y cells treated with 6-OHDA or overexpressed α-synuclein. Cleaved caspase-3 levels significantly increased in cells treated with 6-OHDA or overexpressed α-synuclein. 6-OHDA or α-synuclein overexpression that induced cleaved caspase-3 levels to increase was reduced by MANF treatment. In addition, MANF treatment upregulated GRP78 expressions in cells treated with 6-OHDA or overexpressed α-synuclein, and RNAi knockdown for GRP78 could block the MANF induced cell survival from 6-OHDA treatment. Furthermore, GRP78 overexpression inhibited 6-OHDA-induced apoptosis. Our data suggest that MANF inhibits apoptosis induced by 6-OHDA and overexpressed α-synuclein in SH-SY5Y cells via upregulating GRP78 in the transcriptional pattern.
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