The σ1 receptor regulates accumulation of GM1 ganglioside-enriched autophagosomes in astrocytes

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• 作者：Rika Kasahara^a ; Naoki Yamamoto^a ; ^b ; ^{na-yamam@hokuriku-u.ac.jp} ; Kenji Suzuki^c ; Kazuya Sobue^d
• 关键词：σ1R ; sigma (σ)-1 receptor ; Aβ ; amyloid β-protein ; AD ; alzheimer disease ; APP ; amyloid precursor protein ; CTX-HRP ; Horseradish peroxidase-cholera toxin B subunit ; DMEM ; Dulbecco&rsquo ; s modified Eagle&rsquo ; s medium ; DR ; dopamine receptor ; DRMs ; detergent-resistant membrane microdomains ; ERK ; extracellular signal-regulated kinase ; FBS ; fetal bovine serum ; GM1 ; GM1 ganglioside ; PBS ; phosphate-buffered saline ; PDMP ; (± ; )-threo-1-phenyl-2-decanoylamine-3-morpholino-1-propanol hydrochloride ; PF
• 刊名：Neuroscience
• 出版年：2017
• 出版时间：6 January 2017
• 年：2017
• 卷：340
• 期：Complete
• 页码：176-187
• 全文大小：1599 K
• 卷排序：340

文摘

GM1 gangliosides (GM1) are acidic glycosphingolipids that are present in cell membranes and lipid raft domains, being particularly abundant in central nervous systems. GM1 participate in modulating cell membrane properties, intercellular recognition, cell regulation, and signaling. We previously demonstrated that GM1 are expressed inside astrocytes but not on the cell surface. We investigated whether the antipsychotic drug haloperidol induces GM1 expression in astrocytes, and found that the expression of GM1 was significantly upregulated by haloperidol in the intracellular vesicles of cultured astrocytes. The effects of haloperidol on GM1 expression acted through the σ1 receptor (σ1R), but not the dopamine-2 receptor. Inhibition of the ERK pathway blocked the induction of GM1 through the σ1R by haloperidol. Interestingly, this increase in GM1 expression induced the accumulation of autophagosomes in astrocytes. Moreover, the effect of haloperidol on the σ1R induced a decrease in GM1 in the cellular membrane of astrocytes. These findings suggested that the effects of haloperidol on the σ1R induced GM1 accumulation in the autophagosomes of astrocytes through activating the ERK pathway and a decrease in GM1 expression on the cell surface.