Acetoacetate is a trigger of NLRP3 inflammasome activation in bovine peripheral blood mononuclear cells

被引:6
作者
Onizawa, Yuri [1 ]
Katoh, Taiga [1 ]
Miura, Ryotaro [2 ]
Konda, Kunitoshi [3 ]
Noguchi, Tatsuo [4 ]
Iwata, Hisataka [1 ]
Kuwayama, Takehito [1 ]
Hamano, Seizo [5 ]
Shirasuna, Koumei [1 ]
机构
[1] Tokyo Univ Agr, Dept Anim Sci, Atsugi, Kanagawa 2430034, Japan
[2] Nippon Vet & Life Sci Univ, Dept Vet Med, Musashino, Tokyo 1808602, Japan
[3] Kanagawa Prefectural Livestock Ind Technol Ctr, Ebina, Kanagawa 2430417, Japan
[4] Tokyo Univ Agr, Univ Farm, Shizuoka 4180109, Japan
[5] Artificial Inseminat Assoc Japan, Shinagawa Ku, Tokyo 1350041, Japan
关键词
Acetoacetate; beta-hydroxybutyrate; NLRP3; inflammasome; Repeat breeder cows; BETA-HYDROXYBUTYRATE; DAIRY-COWS; MECHANISM; ENDOMETRIUM; METABOLITE; EXPRESSION; PREGNANCY; CYTOKINES; IMMUNITY; DENSITY;
D O I
10.1016/j.vetimm.2021.110370
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Repeat breeding, which is non-pregnancy following three or more breeding attempts, is a serious reproductive disorder in cattle. In the present study, metabolomic profiling was used to identify metabolites in the blood plasma of repeat breeder cows (RBCs) and non-RBCs. Metabolomic analysis showed that acetoacetate (AcAc), a ketone body, was detected in RBCs, but not in non-RBCs. In contrast, beta-hydroxybutyrate (BHB) was at similar levels in both RBCs and non-RBCs. We hypothesized that an imbalance of AcAc and BHB induces abnormal inflammatory conditions, especially the NLRP3 inflammasome, which regulates sterile inflammation to control interleukin (IL)-1 beta secretion, and may be associated with repeat breeding in cattle. To investigate this hypothesis, blood samples were collected from both non-RBCs and RBCs on day 7 of the estrous cycle. The mRNA expression of IL1B in peripheral blood mononuclear cells (PBMCs) was observed to be higher in RBCs than in non-RBCs. To test the effects of AcAc and BHB on inflammatory responses, blood samples were collected from healthy cows and PBMCs were isolated. PBMCs were treated with AcAc and BHB to investigate the activation of the NLRP3 inflammasome (complex of NLRP3, ASC, and caspase-1) and IL-1 beta secretion. AcAc treatment resulted in higher protein and/or mRNA expression of NLRP3 and IL-1 beta in PBMCs. Moreover, AcAc increased the co-localization of NLRP3 and ASC and stimulated caspase-1 activation, indicating the formation of the platform of the NLRP3 inflammasome. Addition of specific NLRP3 inhibitor, MCC950, suppressed AcAc stimulation-induced IL-1 beta secretion. Contrary to the effects of AcAc, BHB treatment suppressed the activation of NLRP3 inflammasome and IL-1 beta secretion in response to AcAc and typical NLRP3 inflammasome triggers. These findings demonstrate that AcAc can potentially trigger NLRP3 inflammasome activation, resulting in IL-1 beta secretion, and that these in-flammatory responses are suppressed by BHB in bovine PBMCs. In addition, the imbalance between AcAc and BHB with higher levels of IL-1 beta may be associated with repeat breeding in cattle.
引用
收藏
页数:8
相关论文
共 50 条
  • [41] Research Progress of Mitochondrial Mechanism in NLRP3 Inflammasome Activation and Exercise Regulation of NLRP3 Inflammasome
    Zhang, Tan
    Ding, Shuzhe
    Wang, Ru
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (19)
  • [42] A role for mitochondria in NLRP3 inflammasome activation
    Zhou, Rongbin
    Yazdi, Amir S.
    Menu, Philippe
    Tschopp, Juerg
    [J]. NATURE, 2011, 469 (7329) : 221 - 225
  • [43] Dicer regulates activation of the NLRP3 inflammasome
    Ojcius, David M.
    Jafari, Ardavan
    Yeruva, Laxmi
    Schindler, Christian W.
    Abdul-Sater, Ali A.
    [J]. PLOS ONE, 2019, 14 (04):
  • [44] Molecular Mechanism of NLRP3 Inflammasome Activation
    Jin, Chengcheng
    Flavell, Richard A.
    [J]. JOURNAL OF CLINICAL IMMUNOLOGY, 2010, 30 (05) : 628 - 631
  • [45] NLRP3 inflammasome activation in response to metals
    Huang, Wanyi
    Zhang, Ziqi
    Qiu, Yueyang
    Gao, Yuan
    Fan, Yongqiang
    Wang, Qiang
    Zhou, Qing
    [J]. FRONTIERS IN IMMUNOLOGY, 2023, 14
  • [46] NLRP3 inflammasome activation and cell death
    Huang, Yi
    Xu, Wen
    Zhou, Rongbin
    [J]. CELLULAR & MOLECULAR IMMUNOLOGY, 2021, 18 (09) : 2114 - 2127
  • [47] Mitochondrial DNA in NLRP3 inflammasome activation
    Qiu, Yanbing
    Huang, Yumei
    Chen, Meilin
    Yang, Yuqin
    Li, Xiaoxu
    Zhang, Wenling
    [J]. INTERNATIONAL IMMUNOPHARMACOLOGY, 2022, 108
  • [48] Mechanism and Regulation of NLRP3 Inflammasome Activation
    He, Yuan
    Hara, Hideki
    Nunez, Gabriel
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2016, 41 (12) : 1012 - 1021
  • [49] Vimentin regulates activation of the NLRP3 inflammasome
    dos Santos, Gimena
    Rogel, Micah R.
    Baker, Margaret A.
    Troken, James R.
    Urich, Daniela
    Morales-Nebreda, Luisa
    Sennello, Joseph A.
    Kutuzov, Mikhail A.
    Sitikov, Albert
    Davis, Jennifer M.
    Lam, Anna P.
    Cheresh, Paul
    Kamp, David
    Shumaker, Dale K.
    Budinger, G. R. Scott
    Ridge, Karen M.
    [J]. NATURE COMMUNICATIONS, 2015, 6
  • [50] A novel mechanism for NLRP3 inflammasome activation
    Zhang, Tan
    Zhao, Jingyao
    Liu, Tiemin
    Cheng, Wei
    Wang, Yibing
    Ding, Shuzhe
    Wang, Ru
    [J]. METABOLISM OPEN, 2022, 13