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Identification of Sucrose Non-Fermenting-Related Kinase (SNRK) as a Suppressor of Adipocyte Inflammation

机译:蔗糖非发酵相关激酶(SNRK)作为脂肪细胞炎症抑制因子的鉴定

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摘要

In this study, the role of sucrose non-fermenting-related kinase (SNRK) in white adipocyte biology was investigated. SNRK is abundantly expressed in adipose tissue, and the expression level is decreased in obese mice. SNRK expression is repressed by inflammatory signals but increased by insulin sensitizer in cultured adipocytes. In vivo, adipose tissue SNRK expression can be decreased by lipid injection but enhanced by macrophage ablation. Knocking down SNRK in cultured adipocytes activates both JNK and IKKp pathways as well as promotes lipolysis. Insulin-stimulated Akt phosphorylation and glucose uptake are impaired in SNRK knockdown adipocytes. Phosphoproteomic analysis with SNRK knockdown adipocytes revealed significantly decreased phosphorylation of 49 proteins by 25% or more, which are involved in various aspects of adipocyte function with a clear indication of attenuated mTORCl signaling. Phosphorylation of 43 proteins is significantly increased by onefold or higher, among which several proteins are known to be involved in inflammatory pathways. The inflammatory responses in SNRK knockdown adipocytes can be partially attributable to defective mTORCl signaling, since rapamycin treatment activates IKKp and induces lipolysis in adipocytes. In summary, SNRK may act as a suppressor of adipocyte inflammation and its presence is necessary for maintaining normal adipocyte function.
机译:在这项研究中,研究了蔗糖非发酵相关激酶(SNRK)在白色脂肪细胞生物学中的作用。 SNRK在脂肪组织中大量表达,并且在肥胖小鼠中表达水平降低。在培养的脂肪细胞中,SNRK表达受炎性信号抑制,但受胰岛素敏化剂增加。在体内,通过脂质注射可降低脂肪组织的SNRK表达,但通过巨噬细胞消融可增强该表达。敲除培养的脂肪细胞中的SNRK可激活JNK和IKKp途径,并促进脂解作用。 SNRK组合型脂肪细胞中胰岛素刺激的Akt磷酸化和葡萄糖摄取受损。用SNRK敲除脂肪细胞进行的蛋白质组学分析表明,49种蛋白质的磷酸化显着降低了25%或更多,这与脂肪细胞功能的各个方面有关,并清楚显示mTORC1信号减弱。 43种蛋白质的磷酸化显着增加了一倍或更高,其中已知有几种蛋白质与炎症途径有关。由于雷帕霉素治疗激活了IKKp并诱导了脂肪细胞的脂解作用,因此SNRK抑制的脂肪细胞中的炎症反应可以部分归因于mTORC1信号缺陷。总之,SNRK可以作为脂肪细胞炎症的抑制剂,并且它的存在对于维持正常的脂肪细胞功能是必需的。

著录项

  • 来源
    《Diabetes》 |2013年第7期|2396-2409|共14页
  • 作者单位

    Hallett Center for Diabetes and Endocrinology, Rhode Island Hospital, Warren Alpert Medical School of Brown University, Providence, Rhode Island,Department of Geriatric Endocrinology, Jiangsu Province Hospital, Nanjing Medical University, Nanjing, China;

    Hallett Center for Diabetes and Endocrinology, Rhode Island Hospital, Warren Alpert Medical School of Brown University, Providence, Rhode Island,Department of Medicine and Therapeutics, The Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China;

    Department of Molecular Pharmacology and Physiology, Brown University, Providence, Rhode Island;

    Department of Geriatric Endocrinology, Jiangsu Province Hospital, Nanjing Medical University, Nanjing, China;

    Hallett Center for Diabetes and Endocrinology, Rhode Island Hospital, Warren Alpert Medical School of Brown University, Providence, Rhode Island;

    Department of Medicine and Therapeutics, The Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China;

    Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, Rhode Island,Department of Chemistry, Brown University, Providence, Rhode Island;

    Hallett Center for Diabetes and Endocrinology, Rhode Island Hospital, Warren Alpert Medical School of Brown University, Providence, Rhode Island,Pathobiology Program, Brown University, Providence, Rhode Island;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:46:26

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