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Updated: May 1, 2026

Differentiated Mouse Adipocytes in Primary Culture: A Model of Insulin Resistance
Published on: February 17, 2023
IL-34 is associated with obesity, chronic inflammation, and insulin resistance
Eun-Ju Chang1, Seul Ki Lee, Young Sook Song
1Departments of Biomedical Sciences (E.-J.C.) and Physiology (S.K.L., Y.S.S., Y.J.J.), Cell Dysfunction Research Center, and Departments of Family Medicine (H.S.P.), Plastic Surgery (J.P.H.), and Obstetrics and Gynecology (A.R.K., D.Y.K., J.-H.K.), University of Ulsan College of Medicine, Seoul 138-736, Korea; and Departments of Family Medicine (Y.J.L.) and General Surgery (Y.-S.H.), Inha University, College of Medicine, Incheon 402-751, Korea.
Objectives:
IL-34 is a recently identified alternative ligand for colony-stimulating factor-1 (CSF-1) receptor. IL-34 and CSF-1 are regulators of differentiation, proliferation, and survival in mononuclear phagocytes. Here, we investigated the IL-34 serum concentration and expression in human adipose tissues and any associations with insulin resistance.
Methods:
We recruited 19 nondiabetic obese women, 9 type 2 diabetic women, and 27 normal-weight women. Metabolic parameters, abdominal fat distribution, serum IL-34 concentration, and IL-34 mRNA expression were measured in abdominal sc adipose tissue (SAT) and visceral adipose tissue (VAT). In addition, the expression/secretion and putative effects of IL-34 were assessed in human differentiated adipocytes. Serum IL-34 concentration was measured before and 5 to 9 months after laparoscopic Roux-en-Y gastric bypass surgery was performed on the 20 obese patients.
Results:
Regardless of diabetes status, obese patients demonstrated significantly higher serum IL-34 concentrations than controls. Serum IL-34 was significantly and positively correlated with insulin resistance-related metabolic parameters. IL-34 mRNA was significantly higher in VAT than SAT. IL-34 was expressed in adipocytes as well as nonadipocytes, and expression was significantly higher during adipogenesis. In differentiated adipocytes, the expression/secretion of IL-34 was enhanced by TNFα and IL-1β. In addition, IL-34 augmented fat accumulation and inhibited the stimulatory effects of insulin on glucose transport. Moreover, serum IL-34 was significantly decreased after Roux-en-Y gastric bypass-induced weight loss.
Conclusion:
The present study demonstrates, for the first time, that IL-34 is expressed in human adipose tissues and the circulating concentration is significantly elevated in obese patients. This suggests that IL-34 is associated with insulin resistance.
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