Role of irisin in physiology and pathology

被引:58
|
作者
Liu, Shiqiang [1 ]
Cui, Fengqi [1 ]
Ning, Kaiting [1 ]
Wang, Zhen [2 ]
Fu, Pengyu [3 ]
Wang, Dongen [1 ]
Xu, Huiyun [1 ,4 ]
机构
[1] Northwestern Polytech Univ, Sch Life Sci, Key Lab Space Biosci & Biotechnol, Xian, Peoples R China
[2] Northwest Univ, Xian Int Med Ctr Hosp Affiliated, Xian, Peoples R China
[3] Northwestern Polytech Univ, Dept Phys Educ, Xian, Peoples R China
[4] Northwestern Polytech Univ, Res Ctr Special Environm Biomech & Med Engn, Xian, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
irisin; beige fat; musculoskeletal homeostasis; cancer; liver; cardiovascular diseases; ALPHA-V INTEGRIN; INDEPENDENT ACTIVATION; MITOCHONDRIAL FISSION; PI3K/AKT PATHWAY; HORMONE IRISIN; ADIPOSE-TISSUE; CANCER CELLS; EXERCISE; MUSCLE; BONE;
D O I
10.3389/fendo.2022.962968
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Irisin, out-membrane part of fibronectin type III domain-containing 5 protein (FNDC5), was activated by Peroxisome proliferator-activated receptor gamma (PPAR gamma) coactivator-1 alpha (PGC-1 alpha) during physical exercise in skeletal muscle tissues. Most studies have reported that the concentration of irisin is highly associated with health status. For instance, the level of irisin is significantly lower in patients with obesity, osteoporosis/fractures, muscle atrophy, Alzheimer's disease, and cardiovascular diseases (CVDs) but higher in patients with cancer. Irisin can bind to its receptor integrin alpha V/beta 5 to induce browning of white fat, maintain glucose stability, keep bone homeostasis, and alleviate cardiac injury. However, it is unclear whether it works by directly binding to its receptors to regulate muscle regeneration, promote neurogenesis, keep liver glucose homeostasis, and inhibit cancer development. Supplementation of recombinant irisin or exercise-activated irisin might be a successful strategy to fight obesity, osteoporosis, muscle atrophy, liver injury, and CVDs in one go. Here, we summarize the publications of FNDC5/irisin from PubMed/Medline, Scopus, and Web of Science until March 2022, and we review the role of FNDC5/irisin in physiology and pathology.
引用
收藏
页数:12
相关论文
共 50 条
  • [1] Physiology and role of irisin in glucose homeostasis
    Perakakis, Nikolaos
    Triantafyllou, Georgios A.
    Manuel Fernandez-Real, Jose
    Huh, Joo Young
    Park, Kyung Hee
    Seufert, Jochen
    Mantzoros, Christos S.
    NATURE REVIEWS ENDOCRINOLOGY, 2017, 13 (06) : 324 - 337
  • [2] Physiology and role of irisin in glucose homeostasis
    Nikolaos Perakakis
    Georgios A. Triantafyllou
    José Manuel Fernández-Real
    Joo Young Huh
    Kyung Hee Park
    Jochen Seufert
    Christos S. Mantzoros
    Nature Reviews Endocrinology, 2017, 13 : 324 - 337
  • [3] The Role of Interventional Irisin on Heart Molecular Physiology
    Alzoughool, Foad
    Al-Zghoul, Mohammad Borhan
    Ghanim, Bayan Y.
    Gollob, Michael
    Idkaidek, Nasir
    Qinna, Nidal A.
    PHARMACEUTICALS, 2022, 15 (07)
  • [4] Role of Globotriaosylceramide in Physiology and Pathology
    Celi, Ana Beatriz
    Goldstein, Jorge
    Rosato-Siri, Maria Victoria
    Pinto, Alipio
    FRONTIERS IN MOLECULAR BIOSCIENCES, 2022, 9
  • [5] The role of pathology and physiology in preventive medicine
    Bierring, WL
    JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1910, 55 : 554 - 557
  • [6] Role of microglia: From physiology to pathology
    Neher, Jonas
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2021, 429
  • [7] The role of cathepsins in ocular physiology and pathology
    Im, Eunok
    Kazlauskas, Andrius
    EXPERIMENTAL EYE RESEARCH, 2007, 84 (03) : 383 - 388
  • [8] The role of EpCAM in physiology and pathology of the epithelium
    Martowicz, Agnieszka
    Seeber, Andreas
    Untergasser, Gerold
    HISTOLOGY AND HISTOPATHOLOGY, 2016, 31 (04) : 349 - 355
  • [9] Role of serotonin in gastrointestinal physiology and pathology
    Cirillo, C.
    Berghe, R. Vanden
    Tack, J.
    MINERVA ENDOCRINOLOGICA, 2011, 36 (04) : 311 - 324
  • [10] The metabolic role of GIP: Physiology and pathology
    Morgan, LM
    BIOCHEMICAL SOCIETY TRANSACTIONS, 1996, 24 (02) : 585 - 591