Wingless-type inducible signaling pathway protein-1 (WISP1) adipokine and glucose homeostasis.
Habib YaribeygiStephen L AtkinAmir Hossein SahebkarPublished in: Journal of cellular physiology (2019)
Whilst the growing global prevalence of diabetes mellitus is a major healthcare problem, the exact pathophysiology of insulin resistance leading to diabetes mellitus remains unclear. Studies have confirmed that increased adiposity is linked to lower insulin sensitivity through the expression and release of adipocyte-derived proteins such as adipokines. Wingless-type (Wnt) inducible signaling pathway protein-1 (WISP1) is a newly identified adipokine that has important roles in many molecular pathways and cellular events, with the suggestion that WISP1 adipokine is closely correlated to the progression of insulin resistance. Studies have shown that circulatory levels of WISP adipokine are higher in obese patients accompanied with increased insulin resistance. However, the exact role of WISP1 adipokine in the induction of insulin resistance is not completely understood. In this review, we detail the latest evidence showing that the WIPS1 adipokine impairs glucose homeostasis and induces diabetes mellitus.
Keyphrases
- insulin resistance
- adipose tissue
- signaling pathway
- high fat diet
- metabolic syndrome
- glycemic control
- obese patients
- skeletal muscle
- polycystic ovary syndrome
- type diabetes
- healthcare
- high fat diet induced
- bariatric surgery
- blood glucose
- poor prognosis
- binding protein
- epithelial mesenchymal transition
- density functional theory
- stem cells
- pi k akt
- risk factors
- amino acid
- protein protein
- cell proliferation
- roux en y gastric bypass
- gastric bypass
- small molecule
- health insurance
- weight loss
- molecular dynamics
- case control
- extracorporeal membrane oxygenation
- body mass index