Abstract | SCOPE: METHODS AND RESULTS: Mice with Tsc1 deletion in myeloid cells (MTsc1KO) and littermate controls (MTsc1WT) were fed with HFD for 8 weeks and evaluated for body weight, glucose homeostasis, and adipose tissue inflammation. MTsc1KO mice were protected from HFD-induced obesity and glucose intolerance. MTsc1KO, however, displayed, independently of the diet, abnormal behavior, episodes of intense movement, and muscle spasms followed by temporary paralysis. To investigate whether obesity protection was due to myeloid cells Tsc1 deletion, bone marrow was transplanted from MTsc1WT and MTsc1KO into irradiated C57BL6/J mice. Mice transplanted with MTsc1KO bone marrow displayed reduced body weight gain, adiposity, and inflammation, and enhanced energy expenditure, glucose tolerance and adipose tissue M2 macrophage content upon HFD feeding, in the absence of abnormal behavior. In vitro, Tsc1 deletion increased in a mTORC1-dependent manner macrophage polarization to M2 profile and mRNA levels of fatty acid binding protein 4 and PPARĪ³. CONCLUSION: Constitutive mTORC1 activation in myeloid cells protects mice from HFD-induced obesity, adipose tissue inflammation, and glucose intolerance by promoting macrophage polarization to M2 pro-resolution profile and increasing energy expenditure.
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Authors | Vivian A Paschoal, Thiago Belchior, Mariane T Amano, Marina Burgos-Silva, Albert S Peixoto, Juliana Magdalon, Thayna S Vieira, Maynara L Andrade, Mayara F Moreno, Patricia Chimin, Niels O Câmara, William T Festuccia |
Journal | Molecular nutrition & food research
(Mol Nutr Food Res)
Vol. 62
Issue 17
Pg. e1800283
(09 2018)
ISSN: 1613-4133 [Electronic] Germany |
PMID | 30001482
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
Chemical References |
- Cytokines
- Tsc1 protein, mouse
- Tuberous Sclerosis Complex 1 Protein
- Mechanistic Target of Rapamycin Complex 1
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Topics |
- Adipose Tissue
(pathology, physiology)
- Animals
- Cytokines
(metabolism)
- Diet, High-Fat
(adverse effects)
- Gene Expression Regulation
- Macrophages
(pathology)
- Male
- Mechanistic Target of Rapamycin Complex 1
(genetics, metabolism)
- Mice, Inbred C57BL
- Mice, Knockout
- Myeloid Cells
(metabolism)
- Obesity
(etiology, genetics)
- Panniculitis
(metabolism, pathology)
- Tuberous Sclerosis Complex 1 Protein
(genetics, metabolism)
- Weight Gain
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