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核受体过氧化物酶体增殖物激活受体-γ通过涉及线粒体和振荡 Ca2+波的机制促进少突胶质细胞分化。

The nuclear receptor peroxisome proliferator-activated receptor-γ promotes oligodendrocyte differentiation through mechanisms involving mitochondria and oscillatory Ca2+ waves.

出版信息

Biol Chem. 2013 Dec;394(12):1607-14. doi: 10.1515/hsz-2013-0152.

Abstract

Peroxisome proliferator-activated receptor-γ (PPAR-γ) is one of the most studied nuclear receptor since its identification as a target to treat metabolic and neurological diseases. In addition to exerting anti-inflammatory and neuroprotective effects, PPAR-γ agonists, such as the insulin-sensitizing drug pioglitazone, promote the differentiation of oligodendrocytes (OLs), the myelin-forming cells of the central nervous system (CNS). In addition, PPAR-γ agonists increase OL mitochondrial respiratory chain activity and OL's ability to respond to environmental signals with oscillatory Ca2+ waves. Both OL maturation and oscillatory Ca2+ waves are prevented by the mitochondrial inhibitor rotenone and restored by PPAR-γ agonists, suggesting that PPAR-γ promotes myelination through mechanisms involving mitochondria.

摘要

过氧化物酶体增殖物激活受体-γ (PPAR-γ) 是研究最多的核受体之一,因其被确定为治疗代谢和神经疾病的靶点。除了发挥抗炎和神经保护作用外,PPAR-γ 激动剂,如胰岛素增敏药物吡格列酮,还能促进少突胶质细胞 (OLs) 的分化,OLs 是中枢神经系统 (CNS) 的髓鞘形成细胞。此外,PPAR-γ 激动剂增加 OL 线粒体呼吸链活性和 OL 对环境信号产生振荡 Ca2+波的能力。线粒体抑制剂鱼藤酮可阻止 OL 成熟和振荡 Ca2+波,而 PPAR-γ 激动剂则可恢复这一过程,表明 PPAR-γ 通过涉及线粒体的机制促进髓鞘形成。

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