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Page 62

Volume 9

Journal of Obesity & Weight Loss Therapy

ISSN: 2165-7904

JOINT EVENT

Childhood Obesity 2019

Diabetes Conference 2019

March 18-19, 2019

&

3

rd

World Congress on

Diabetes and Obesity

12

th

International Conferences on

Childhood Obesity and Nutrition

March 18-19, 2019 | Rome, Italy

Adipose tissue-resident macrophages (M2-like) regulates proliferation of white and beige progenitors

Nawaz A

University of Toyama, Japan

P

revious reports suggested that adipose tissue macrophages are involved in maintaining insulin sensitivity in

adipocytes along with improvement in metabolic genes. Nonetheless, it is largely unknown how depletion of

M2-like macrophages regulates insulin sensitivity and adipocyte progenitor (AP) proliferation. To understand the

role of M2-like macrophages in white adipose tissue (WAT), we generated CD206DTR mice based on transgenic

expression of diphtheria toxin receptor under the control of the CD206(+) promoter to specifically deplete CD206

M2-like macrophages. Partial depletion of CD206 M2-like macrophages resulted in the generation of smaller

adipocytes, upregulated expression of metabolically favorable genes and enhanced insulin sensitivity in both chow

and high-fat diet-fed CD206-reduced mice. In vivo and in vitro studies revealed that Tgf1, abundantly expressed

in CD206 M2-like macrophages, regulate AP differentiation and proliferation. Flow cytometry analysis revealed that

the number of APs was increased and cyclin gene expression levels in the AP fraction were up-regulated. To validate

this hypothesis, we generated genetically engineered mice in which CD206 specific Tgfβ1 was knocked out after

tamoxifen treatment. Increased number of APs and smaller adipocytes were observed in the CD206 specific Tgfβ1

knockout mice, suggesting that CD206 cell-specific deletion of Tgfβ1 resulted in the enhanced proliferation of AP.

Previous studies had shown that type 2 cytokines and M2 macrophages induce cold-induced browning in inguinal

WAT (ingWAT) by producing catecholamines. Exactly how the conditional and partial depletion of CD206 M2-

like macrophages regulates the cold-induced browning of ingWAT, however, remains unknown. We also examined

the role of CD206 M2-like macrophages in the cold-induced browning of WAT and found that partial depletion

of CD206 M2-like macrophages caused an increase in the number of beige progenitors and also enhanced their

proliferation in ingWAT in response to cold. Thus, we concluded that CD206 M2-like macrophages inhibit the

proliferation of white and beige progenitors.

Keywords:

Adipocyte progenitors, adipose tissue macrophages, beige adipocyte, insulin sensitivity.

J Obes Weight Loss Ther 2019, Volume 9

DOI: 10.4172/2165-7904-C1-091