Brown adipose tissue monocytes support tissue expansion.
Brown adipose tissue monocytes support tissue expansion.
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DOI:
10.1038/s41467-021-25616-1
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发表时间:
2021-09-06
影响因子:
16.6
通讯作者:
Ivanov S
中科院分区:
文献类型:
--
作者:
Gallerand A;Stunault MI;Merlin J;Luehmann HP;Sultan DH;Firulyova MM;Magnone V;Khedher N;Jalil A;Dolfi B;Castiglione A;Dumont A;Ayrault M;Vaillant N;Gilleron J;Barbry P;Dombrowicz D;Mack M;Masson D;Bertero T;Becher B;Williams JW;Zaitsev K;Liu Y;Guinamard RR;Yvan-Charvet L;Ivanov S
Monocytes are part of the mononuclear phagocytic system. Monocytes play a central role during inflammatory conditions and a better understanding of their dynamics might open therapeutic opportunities. In the present study, we focused on the characterization and impact of monocytes on brown adipose tissue (BAT) functions during tissue remodeling. Single-cell RNA sequencing analysis of BAT immune cells uncovered a large diversity in monocyte and macrophage populations. Fate-mapping experiments demonstrated that the BAT macrophage pool requires constant replenishment from monocytes. Using a genetic model of BAT expansion, we found that brown fat monocyte numbers were selectively increased in this scenario. This observation was confirmed using a CCR2-binding radiotracer and positron emission tomography. Importantly, in line with their tissue recruitment, blood monocyte counts were decreased while bone marrow hematopoiesis was not affected. Monocyte depletion prevented brown adipose tissue expansion and altered its architecture. Podoplanin engagement is strictly required for BAT expansion. Together, these data redefine the diversity of immune cells in the BAT and emphasize the role of monocyte recruitment for tissue remodeling. Adipose tissue is composed of a number of adipocytes and a number of other cells including immune cells. Here the authors use single-cell sequencing of murine brown adipose tissue immune cells and describe multiple macrophage and monocyte subsets and show that monocytes contribute to brown adipose tissue expansion.
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DOI:
10.1084/jem.20160800
发表时间:
2016-10-17
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Chong SZ;Evrard M;Devi S;Chen J;Lim JY;See P;Zhang Y;Adrover JM;Lee B;Tan L;Li JL;Liong KH;Phua C;Balachander A;Boey A;Liebl D;Tan SM;Chan JK;Balabanian K;Harris JE;Bianchini M;Weber C;Duchene J;Lum J;Poidinger M;Chen Q;Rénia L;Wang CI;Larbi A;Randolph GJ;Weninger W;Looney MR;Krummel MF;Biswas SK;Ginhoux F;Hidalgo A;Bachelerie F;Ng LG
通讯作者:
Ng LG
影响因子:
29
作者:
Amano SU;Cohen JL;Vangala P;Tencerova M;Nicoloro SM;Yawe JC;Shen Y;Czech MP;Aouadi M
通讯作者:
Aouadi M
影响因子:
32.4
作者:
Croxford, Andrew L.;Lanzinger, Margit;Becher, Burkhard
通讯作者:
Becher, Burkhard
影响因子:
30.5
作者:
通讯作者:
--
影响因子:
9
作者:
Abdullahi A;Auger C;Stanojcic M;Patsouris D;Parousis A;Epelman S;Jeschke MG
通讯作者:
Jeschke MG