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Isolation, Expansion, and Adipogenic Induction of CD34+CD31+ Endothelial Cells from Human Omental and Subcutaneous Adipose Tissue
Published on: July 17, 2018
High expression of CD52 in adipocytes: a potential therapeutic target for obesity with type 2 diabetes
Rui Mao1, Fan Yang2, Yu Zhang1
1The Center of Gastrointestinal and Minimally Invasive Surgery, The Third People's Hospital of Chengdu, Affiliated Hospital of Southwest Jiaotong University, Chengdu 610031, China.
Abstract:
The aim of the present study was to evaluate the involvement of CD52 in adipocytes as well as to explore its effect on type 2 diabetes mellitus (T2DM), and to improve our understanding of the potential molecular events of obesity with type 2 diabetes. Global changes in the CD52 expression patterns were detected in adipocytes and preadipocytes derived from obese and lean individuals. In particular, CD52 was identified as significantly differentially upregulated and was analyzed, both in vitro and in vivo, using various approaches. In vitro experiments, CD52 was a significantly up-regulated mRNA in mature adipocytes and preadipocytes. In addition, CD52 gradually increased with the differentiation of preadipocytes. In vivo experiments, the expression of CD52 in high-fat diet (HFD) -fed mice tended to be higher than that in regular diet (RD) -fed mice. Further analysis showed that CD52 expression was positively correlated with Smad3 and TGF-β in mice, and the downregulation of CD52 was accompanied by increased glucose tolerance and insulin sensitivity. Moreover, a comparison of CD4+CD52high T cells and CD4+CD52low T cells showed that many T2DM-related genes were aberrantly expressed. Overall, CD52 may functioned as an important potential target for obesity with T2DM via TGF-β/Smad3 axis.
Insights
CD52 is upregulated in obesity and type 2 diabetes (T2DM). Downregulating CD52 improves glucose tolerance and insulin sensitivity, suggesting it
Area of Science:
- Metabolism
- Immunology
- Endocrinology
Background:
- Obesity and type 2 diabetes mellitus (T2DM) are complex metabolic disorders.
- Understanding the molecular mechanisms linking obesity and T2DM is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the role of CD52 in adipocytes.
- To explore the association between CD52 and T2DM in the context of obesity.
- To elucidate potential molecular pathways involved in obesity with T2DM.
Main Methods:
- Analysis of CD52 expression in adipocytes and preadipocytes from lean and obese individuals.
- In vitro studies on CD52 mRNA levels during adipocyte differentiation.
- In vivo studies using high-fat diet (HFD)-fed mice.
- Correlation analysis of CD52 with TGF-β/Smad3 signaling pathway.
- Comparison of gene expression in CD4+ T cell subsets.
Main Results:
- CD52 mRNA was significantly upregulated in mature adipocytes and preadipocytes, increasing with differentiation.
- CD52 expression was higher in HFD-fed mice compared to regular diet-fed mice.
- CD52 expression positively correlated with Smad3 and TGF-β.
- Downregulation of CD52 improved glucose tolerance and insulin sensitivity.
- Aberrant expression of T2DM-related genes was observed in CD4+CD52high T cells compared to CD4+CD52low T cells.
Conclusions:
- CD52 is implicated in the pathophysiology of obesity with T2DM.
- CD52 may regulate T2DM through the TGF-β/Smad3 signaling pathway.
- CD52 represents a potential therapeutic target for obesity and T2DM.
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