Quantum dots protect against MPP+-induced neurotoxicity in a cell model of Parkinson’s disease through autophagy induction
Quantum dots protect against MPP+-induced neurotoxicity in a cell model of Parkinson’s disease through autophagy induction
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DOI:
10.1007/s11426-016-0103-7
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发表时间:
2016-10
期刊:
影响因子:
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通讯作者:
Lu Wang;Xiaoming Li;Yuping Han;Ting Wang;Yun Zhao;Aldalbahi Ali;Nahed N E El-Sayed;Jiye Shi-Jiye
中科院分区:
文献类型:
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作者:
Lu Wang;Xiaoming Li;Yuping Han;Ting Wang;Yun Zhao;Aldalbahi Ali;Nahed N E El-Sayed;Jiye Shi-Jiye
Autophagy is a basic cellular process that decomposes damaged organelles and aberrant proteins. Dysregulation of autophagy is implicated in pathogenesis of neurodegenerative disorders, including Parkinson’s disease (PD). Pharmacological compounds that stimulate autophagy can provide neuroprotection in models of PD. Nanoparticles have emerged as regulators of autophagy and have been tested in adjuvant therapy for diseases. In this present study, we explore the effects of quantum dots (QDs) that can induce autophagy in a cellular model of Parkinson’s disease. CdTe/CdS/ZnS QDs protect differentiated rat pheochromocytoma PC12 cells from MPP+-induced cell damage, including reduced viability, apoptosis and accumulation of α-Synuclein, a characteristic protein of PD. The protective function of QDs is autophagy-dependent. In addition, we investigate the interaction between quantum dots and autophagic pathways and identify beclin1 as an essential factor for QDs-induced autophagy. Our results reveal new promise of QDs in the theranostic of neurodegenerative diseases.