Protect Effects of Seafood-Derived Plasmalogens Against Amyloid-Beta (1–42) Induced Toxicity via Modulating the Transcripts Related to Endocytosis, Autophagy, Apoptosis, Neurotransmitter Release and Synaptic Transmission in SH-SY5Y Cells.

To investigate the underlying mechanisms of decreased plasmalogens (Pls) levels in neurodegenerative diseases, here the effects of seafood-derived Pls on undifferentiated and differentiated human SH-SY5Y neuroblastoma cells exposed to amyloid-β1–42 was analyzed. Transcriptional profiles indicated th...

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Publicado en:Frontiers in Aging Neuroscience Vol. 13; pp. 1 - 13
Autores principales: Feng, Junli, Song, Gongshuai, Shen, Qing, Chen, Xi, Wang, Qingcheng, Guo, Shunyuan, Zhang, Manman
Formato: Journal Article
Publicado: Frontiers Media S.A. 11/26/2021
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 11/26/2021
      vid: 13
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      pub: Frontiers Media S.A.
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        10.3389/fnagi.2021.773713
        153827252
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        atl: Protect Effects of Seafood-Derived Plasmalogens Against Amyloid-Beta (1–42) Induced Toxicity via Modulating the Transcripts Related to Endocytosis, Autophagy, Apoptosis, Neurotransmitter Release and Synaptic Transmission in SH-SY5Y Cells.
      aug:
        au:
          Feng, Junli
          Song, Gongshuai
          Shen, Qing
          Chen, Xi
          Wang, Qingcheng
          Guo, Shunyuan
          Zhang, Manman
        affil: Zhejiang Province Joint Key Laboratory of Aquatic Products Processing, Collaborative Innovation Center of Seafood Deep Processing, Institute of Seafood, Zhejiang Gongshang University, Hangzhou, China
      sug:
      ab: To investigate the underlying mechanisms of decreased plasmalogens (Pls) levels in neurodegenerative diseases, here the effects of seafood-derived Pls on undifferentiated and differentiated human SH-SY5Y neuroblastoma cells exposed to amyloid-β1–42 was analyzed. Transcriptional profiles indicated that a total of 6,581 differentially expressed genes (DEGs) were significantly identified among different experimental groups, and KEGG analysis indicated that these DEGs were related to AD, endocytosis, synaptic vesicle cycle, autophagy and cellular apoptosis. After Pls treatment, the striking expression changes of ADORA2A , ATP6V1C2 , CELF6 , and SLC18A2 mRNA strongly suggest that Pls exerts a beneficial role in alleviating AD pathology partly by modulating the neurotransmitter release and synaptic transmission at the transcriptional level. Besides these, GPCRs are also broadly involved in Pls-signaling in neuronal cells. These results provide evidence for supporting the potential use of Pls as an effective therapeutic approach for AD.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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