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M1/M2 Macrophages Play Different Roles in Adipogenic Differentiation of PDGFRα+ Preadipocytes In Vitro
Hao Cheng1, Jie Luan1, Dali Mu1
1Breast Plastic and Reconstructive Center, Plastic Surgery Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, 33 Badachu Road, Shijingshan District, Beijing, 100144, People's Republic of China.
Background:
PGGFRα+ preadipocytes are the major subpopulations that can regenerate into adipocytes. Two different types of macrophages exist in the fat tissue: the classically activated macrophage (M1) and the alternatively activated macrophage (M2). In this study, we investigated whether M1/M2 macrophages play distinct roles in adipogenic differentiation of PDGFRα+ preadipocytes.
Methods:
Mouse preadipocytes and macrophages were isolated from C57BL/6 male mice of 6-8 weeks. The culture supernate of M1 and M2 macrophages was collected and co-cultured with the PDGFRα+ preadipocytes. After 3 days, Oil Red O staining was used to evaluate to adipogenic differentiation of PDGFRα+ preadipocytes and the expression of adipogenic-related transcription factors (C/EBP-α, PPARγ) were also tested.
Results:
The results showed that when cultured in vitro, M1 macrophages could significantly suppress the adipogenesis of PDGFRα+ preadipocytes as well as the C/EBP-α and PPARγ expression, but M2 macrophages did not have significant influence on the adipogenesis of PDGFRα+ preadipocytes nor on C/EBP-α and PPARγ expression compared with the control group.
Conclusions:
M1 macrophages significantly suppress PDGFRα+ preadipocyte adipogenesis which provides a possible way to improve adipogenesis and fat retention after fat-free grafting by mitigating acute inflammation and manipulating M1 macrophage levels.
No Level Assigned:
This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266 .
Insights
Classically activated macrophages (M1) suppress adipogenesis in PDGFRα+ preadipocytes. Alternatively activated macrophages (M2) do not significantly affect this process, offering insights into fat tissue regeneration.
Area of Science:
- Adipose tissue biology
- Immunology
- Cell differentiation
Background:
- Platelet-derived growth factor receptor alpha-positive (PDGFRα+) preadipocytes are key for adipocyte regeneration.
- Fat tissue contains two main macrophage types: classically activated (M1) and alternatively activated (M2).
Purpose of the Study:
- To investigate the distinct roles of M1 and M2 macrophages in the adipogenic differentiation of PDGFRα+ preadipocytes.
Main Methods:
- PDGFRα+ preadipocytes and macrophages were isolated from mice.
- Macrophage culture supernatants (M1 and M2) were co-cultured with preadipocytes.
- Adipogenic differentiation was assessed using Oil Red O staining and transcription factor expression (C/EBP-α, PPARγ).
Main Results:
- M1 macrophages significantly inhibited PDGFRα+ preadipocyte adipogenesis and reduced C/EBP-α and PPARγ expression.
- M2 macrophages showed no significant effect on adipogenesis or transcription factor expression compared to controls.
Conclusions:
- M1 macrophages suppress PDGFRα+ preadipocyte differentiation, suggesting potential therapeutic strategies for fat grafting by modulating inflammation and M1 macrophage levels.
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