Placental mesenchymal stem cells restore glucose and energy homeostasis in obesogenic adipocytes

Cell Tissue Res. 2023 Jan;391(1):127-144. doi: 10.1007/s00441-022-03693-y. Epub 2022 Oct 13.

Abstract

Obesity (Ob) depicts a state of energy imbalance(s) being characterized by the accumulation of excessive fat and which predisposes to several metabolic diseases. Mesenchymal stem cells (MSCs) represent a promising option for addressing obesity and its associated metabolic co-morbidities. The present study aims at assessing the beneficial effects of human placental MSCs (P-MSCs) in mitigating Ob-associated insulin resistance (IR) and mitochondrial dysfunction both in vivo and in vitro. Under obesogenic milieu, adipocytes showed a significant reduction in glucose uptake, and impaired insulin signaling with decreased expression of UCP1 and PGC1α, suggestive of dysregulated non-shivering thermogenesis vis-a-vis mitochondrial biogenesis respectively. Furthermore, obesogenic adipocytes demonstrated impaired mitochondrial respiration and energy homeostasis evidenced by reduced oxygen consumption rate (OCR) and blunted ATP/NAD+/NADP+ production respectively. Interestingly, co-culturing adipocytes with P-MSCs activated PI3K-Akt signaling, improved glucose uptake, diminished ROS production, enhanced mitochondrial OCR, improved ATP/NAD+/NADP+ production, and promoted beiging of adipocytes evidenced by upregulated expression of PRDM16, UCP1, and PGC1α expression. In vivo, P-MSCs administration increased the peripheral blood glucose uptake and clearance, and improved insulin sensitivity and lipid profile with a coordinated increase in the ratio of ATP/ADP and NAD+ and NADP+ in the white adipose tissue (WAT), exemplified in WNIN/GR-Ob obese mutant rats. In line with in vitro findings, there was a significant reduction in adipocyte hypertrophy, increased mitochondrial staining, and thermogenesis. Our findings advocate for a therapeutic application of P-MSCs for improving glucose and energy homeostasis, i.e., probably restoring non-shivering thermogenesis towards obesity management.

Keywords: Adipocytes; Beiging phenotype; Energy homeostasis; Human P-MSC therapy; Mitochondrial turnover; Obesogenic milieu.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Adipocytes* / metabolism
  • Animals
  • Energy Metabolism* / physiology
  • Female
  • Glucose Metabolism Disorders / pathology
  • Glucose* / metabolism
  • Homeostasis
  • Humans
  • Insulin Resistance* / physiology
  • Mesenchymal Stem Cells* / metabolism
  • NAD / metabolism
  • NADP / metabolism
  • Obesity* / metabolism
  • Obesity* / pathology
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Placenta* / metabolism
  • Rats

Substances

  • Adenosine Triphosphate
  • Glucose
  • NAD
  • NADP
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Phosphatidylinositol 3-Kinases