Yin and yang of cannabinoid CB1 receptor: CB1 deletion in immune cells causes exacerbation while deletion in non-immune cells attenuates obesity

被引:6
作者
Miranda, Kathryn [1 ]
Becker, William [1 ]
Busbee, Philip B. [1 ]
Dopkins, Nicholas [1 ]
Abdulla, Osama A. [1 ]
Zhong, Yin [1 ]
Zhang, Jiajia [2 ]
Nagarkatti, Mitzi [1 ]
Nagarkatti, Prakash S. [1 ]
机构
[1] Univ South Carolina, Dept Pathol Microbiol & Immunol, Sch Med, Columbia, SC 29209 USA
[2] Univ South Carolina, Arnold Sch Publ Hlth, Epidemiol & Biostat, Columbia, SC USA
关键词
BROWN ADIPOSE-TISSUE; DIET-INDUCED OBESITY; MACROPHAGE POLARIZATION; MEDIATED REGULATION; INSULIN-RESISTANCE; SUPPRESSOR-CELLS; GUT MICROBIOME; ACTIVATION; MICE; INFLAMMATION;
D O I
10.1016/j.isci.2022.104994
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
While blockade of cannabinoid receptor 1 (CB1) has been shown to attenuate diet-induced obesity (DIO), its relative role in different cell types has not been tested. The current study investigated the role of CB1 in immune vs non-immune cells during DIO by generating radiation-induced bone marrow chimeric mice that expressed functional CB1 in all cells except the immune cells or expressed CB1 only in immune cells. CB1(-/-) recipient hosts were resistant to DIO, indicating that CB1 in non-immune cells is necessary for induction of DIO. Interestingly, chimeras with CB1(-/-) in immune cells showed exacerbation in DIO combined with infiltration of bone-marrow-derived macrophages to the brain and visceral adipose tissue, elevated food intake, and increased glucose intolerance. These results demonstrate the opposing role of CB1 in hematopoietic versus non-hematopoietic cells during DIO and suggests that targeting immune CB1 receptors provides a new pathway to ameliorate obesity and related metabolic disorders.
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页数:15
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