Adipose-derived mesenchymal stem cells from obese mice prevent body weight gain and hyperglycemia

Yicheng Qi1, Wen Liu1, Xiangsheng Wang2

  • 1Department of Endocrinology and Metabolism, Renji Hospital, School of Medicine, Shanghai Jiaotong University, No. 160 Pujian Road, Pudong New Area, Shanghai, 200127, China.

Insights

Obese mice treated with their own adipose-derived stem cells (ADSCs) showed reduced weight gain and improved hyperglycemia. These findings suggest autologous ADSCs may effectively treat obesity and related metabolic disorders.

Area of Science:

  • Stem Cell Biology
  • Metabolic Disease Research
  • Obesity and Diabetes Studies

Background:

  • Disease-induced changes in the stem cell microenvironment impact mesenchymal stem cell (MSC) behavior and therapeutic potential.
  • Adipose-derived stem cells (ADSCs) are being investigated for therapeutic applications in metabolic disorders.

Purpose of the Study:

  • To evaluate the therapeutic effects of ADSCs from obese mice with hyperglycemia on body weight and glucose homeostasis.
  • To determine if autologous ADSCs from obese individuals are more effective for treating obesity-related hyperglycemia.

Main Methods:

  • Obese mice on a high-fat diet were injected with phosphate-buffered saline (PBS), normal ADSCs (N-ADSCs), or obese ADSCs (O-ADSCs).
  • Normal mice on standard chow injected with PBS served as controls.
  • Body weight, glucose homeostasis, inguinal fat mass, insulin receptor (INSR) expression, CD90, and monocyte chemoattractant protein 1 (MCP-1) were analyzed.

Main Results:

  • Obese mice treated with O-ADSCs exhibited reduced body weight gain compared to PBS or N-ADSC groups.
  • ADSC treatment, particularly with O-ADSCs, improved obesity-related hyperglycemia.
  • O-ADSC treatment led to reduced inguinal fat, likely due to increased lipolysis, and restored INSR expression in muscle tissue.

Conclusions:

  • Autologous ADSCs from obese individuals demonstrate potential efficacy in treating obesity and associated hyperglycemia.
  • O-ADSCs showed distinct expression profiles (increased CD90, reduced MCP-1) compared to N-ADSCs, suggesting disease-specific adaptations.
  • These findings support the use of autologous ADSCs as a therapeutic strategy for metabolic disorders.

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