Insight into the development of obesity: functional alterations of adipose-derived mesenchymal stem cells.
F LouwenA RitterN N KreisJuping YuanPublished in: Obesity reviews : an official journal of the International Association for the Study of Obesity (2018)
Obesity is associated with a variety of disorders including cardiovascular diseases, diabetes mellitus and cancer. Obesity changes the composition and structure of adipose tissue, linked to pro-inflammatory environment, endocrine/metabolic dysfunction, insulin resistance and oxidative stress. Adipose-derived mesenchymal stem cells (ASCs) have multiple functions like cell renewal, spontaneous repair and homeostasis in adipose tissue. In this review article, we have summarized the recent data highlighting that ASCs in obesity are defective in various functionalities and properties including differentiation, angiogenesis, motility, multipotent state, metabolism and immunomodulation. Inflammatory milieu, hypoxia and abnormal metabolites in obese tissue are crucial for impairing the functions of ASCs. Further work is required to explore the precise molecular mechanisms underlying its alterations and impairments. Based on these data, we suggest that deregulated ASCs, possibly also other mesenchymal stem cells, are important in promoting the development of obesity. Restoration of ASCs/mesenchymal stem cells might be an additional strategy to combat obesity and its associated diseases.
Keyphrases
- insulin resistance
- adipose tissue
- mesenchymal stem cells
- metabolic syndrome
- weight loss
- high fat diet induced
- type diabetes
- high fat diet
- oxidative stress
- skeletal muscle
- polycystic ovary syndrome
- umbilical cord
- weight gain
- bone marrow
- cardiovascular disease
- cell therapy
- bariatric surgery
- glycemic control
- squamous cell carcinoma
- escherichia coli
- dna damage
- electronic health record
- ms ms
- pseudomonas aeruginosa
- ischemia reperfusion injury
- papillary thyroid
- single cell
- staphylococcus aureus
- cardiovascular risk factors
- heat shock protein
- diabetic rats
- childhood cancer