Extracellular Vesicles from Adipose Tissue Could Promote Metabolic Adaptation through PI3K/Akt/mTOR

被引:4
|
作者
Delgadillo-Velazquez, Jaime [1 ]
Mendivil-Alvarado, Herminia [1 ]
Daniel Coronado-Alvarado, Carlos [1 ]
Astiazaran-Garcia, Humberto [1 ,2 ]
机构
[1] Res Ctr Food & Dev CIAD, Coordinat Nutr, Ave Gustavo E Astiazaran 46, Hermosillo 83304, Sonora, Mexico
[2] Univ Sonora, Dept Ciencias Quim Biol, Hermosillo 83000, Sonora, Mexico
关键词
cell communication; exosomes; obesity; insulin resistance; INSULIN-RESISTANCE; SKELETAL-MUSCLE; SIGNALING PATHWAYS; PPAR-GAMMA; EXOSOMES; OBESITY; FAT; ADIPOCYTES; MICROVESICLES; MIR-27A;
D O I
10.3390/cells11111831
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Extracellular vesicles (EVs) are nanoparticles secreted by cells under physiological and pathological conditions, such as metabolic diseases. In this context, EVs are considered potential key mediators in the physiopathology of obesity. It has been reported that EVs derived from adipose tissue (ADEVs) contribute to the development of a local inflammatory response that leads to adipose tissue dysfunction. In addition, it has been proposed that EVs are associated with the onset and progression of several obesity-related metabolic diseases such as insulin resistance. In particular, characterizing the molecular fingerprint of obesity-related ADEVs can provide a bigger picture that better reflects metabolic adaptation though PI3K/Akt/mTOR. Hence, in this review we describe the possible crosstalk communication of ADEVs with metabolically active organs and the intracellular response in the insulin signaling pathway.
引用
收藏
页数:17
相关论文
共 50 条
  • [1] Plasma endothelial cells-derived extracellular vesicles promote wound healing in diabetes through YAP and the PI3K/Akt/mtOR pathway
    Wei, Feng
    Wang, Aixue
    Wang, Qing
    Han, Wenrui
    Rong, Rong
    Wang, Lijuan
    Liu, Sijia
    Zhang, Yimeng
    Dong, Chao
    Li, Yanling
    AGING-US, 2020, 12 (12): : 12002 - 12018
  • [2] PI3K/AKT/mTOR
    Umemura, Shigeki
    Goto, Koichi
    JOURNAL OF THORACIC ONCOLOGY, 2015, 10 (09) : S116 - S117
  • [3] Adipose stem cell exosomes promote mitochondrial autophagy through the PI3K/AKT/mTOR pathway to alleviate keloids
    Liu, Chang
    Khairullina, Liliia
    Qin, Youyou
    Zhang, Yingbo
    Xiao, Zhibo
    STEM CELL RESEARCH & THERAPY, 2024, 15 (01)
  • [4] Follistatin could promote the proliferation of duck primary myoblasts by activating PI3K/Akt/mTOR signalling
    Li, Xinxin
    Liu, Hehe
    Wang, Haohan
    Sun, Lingli
    Ding, Fang
    Sun, Wenqiang
    Han, Chunchun
    Wang, Jiwen
    BIOSCIENCE REPORTS, 2014, 34 : 609 - 620
  • [5] Resistin targets TAZ to promote osteogenic differentiation through PI3K/AKT/mTOR pathway
    Shang, Jingjing
    Yu, Zhentang
    Xiong, Chengwei
    Zhang, Junjie
    Gong, Jinhong
    Yu, Changlin
    Huang, Yong
    Zhou, Xindie
    ISCIENCE, 2023, 26 (07)
  • [6] Immunologic and metabolic consequences of PI3K/AKT/mTOR activation in melanoma
    Nanda, Vashisht G. Y.
    Peng, Weiyi
    Hwu, Patrick
    Davies, Michael A.
    JOURNAL OF TRANSLATIONAL MEDICINE, 2016, 14
  • [7] PI3K/AKT/mTOR pathway in angiogenesis
    Karar, Jayashree
    Maity, Amit
    FRONTIERS IN MOLECULAR NEUROSCIENCE, 2011, 4
  • [8] The PI3K/Akt/mTOR signaling pathway
    Dennis, P. A.
    ANNALS OF ONCOLOGY, 2011, 22 : 19 - 19
  • [9] Overview of the PI3K/Akt/mTOR pathway
    Dennis, P. A.
    ANNALS OF ONCOLOGY, 2008, 19 : 21 - 21
  • [10] The PI3K/AKT/mTOR interactive pathway
    Ersahin, Tulin
    Tuncbag, Nurcan
    Cetin-Atalay, Rengul
    MOLECULAR BIOSYSTEMS, 2015, 11 (07) : 1946 - 1954