Tumor Necrosis Receptor Superfamily Interact with Fusion and Fission of Mitochondria of Adipose Tissue in Obese Patients without Type 2 Diabetes.
Daria SkuratovskaiaAleksandra KomarMaria VulfHung Vu QuangEgor ShunkinElena KirienkovaAnastasiia DakchnevichDanil MalkovPavel ZatolokinLarisa S LitvinovaPublished in: Biomedicines (2021)
Interactions between receptors and ligands of the tumor necrosis factor superfamily (TNFSF) provide costimulatory signals that control the survival, proliferation, differentiation, and effector function of immune cells. All components of the TNF superfamily are associated with NF-kB functions that are not limited to cell death and may promote survival in the face of adipose tissue inflammation in obesity. Inflammation dysfunction of mitochondria is a key factor associated with insulin resistance in obesity. The aim of the study was to analyze the relationship of soluble forms of receptors and ligands of the TNF superfamily in blood plasma with mitochondrial dynamics in adipose tissue (greater omentum (GO) and subcutaneous adipose tissue (Sat)) of obese patients with and without type 2 diabetes mellitus (T2DM). Increased plasma sTNF-R1, sTNF-R2, sTNFRSF8 receptors, and ligands TNFSF12, TNFSF13, TNFSF13B are characteristic of obese patients without T2DM. The TNF-a levels in blood plasma were associated with a decrease in MFN2 gene expression in GO and IL-10 in blood plasma. The TNFSF12 levels contributed to a decrease in glucose levels, a decrease in BMI, and an increase in IL-10 levels by influencing the MFN2 gene expression in GO, which supports mitochondrial fusion.
Keyphrases
- adipose tissue
- obese patients
- insulin resistance
- oxidative stress
- bariatric surgery
- gene expression
- type diabetes
- cell death
- weight loss
- rheumatoid arthritis
- glycemic control
- high fat diet
- roux en y gastric bypass
- gastric bypass
- metabolic syndrome
- high fat diet induced
- weight gain
- body mass index
- dendritic cells
- genome wide identification
- cell proliferation
- immune response
- endoplasmic reticulum
- cardiovascular risk factors
- cell cycle arrest