Lai Jing, Liu Gexiu, Yan Guoyao, He Dongmei, Zhou Ying, Chen Shengting
The First Affiliated Hospital, Jinan University, Guangzhou, Guangdong, China.
Institute of Hematology, School of Medicine, Jinan University, Guangzhou, Guangdong, China.
Biochem Biophys Res Commun. 2015 Jun 26;462(2):105-11. doi: 10.1016/j.bbrc.2015.04.064. Epub 2015 Apr 21.
By investigating the anti-adipogenic effects of WEHI-3 cells - a murine acute myelomonocytic leukemia cell line - we sought to improve the efficiency of hematopoietic stem cell transplantation (HSCT). Analysis of Oil Red O staining and the expression of adipogenic genes, including PPARγ, C/EBPα, FAS and LPL, indicated that WEHI-3 cells significantly inhibited 3T3-L1 mouse preadipocyte cells from differentiating into adipocytes. In vivo, fat vacuoles in mice injected with WEHI-3 cells were also remarkably reduced in the murine bone marrow pimelosis model. Moreover, the key gene in the Rho signaling pathway, ROCKII, and the key gene in the Wnt signaling pathway, β-catenin, were both upregulated compared with the control group. siRNA-mediated knockdown of ROCKII and β-catenin reversed these WEHI-3-mediated anti-adipogenic effects. Taken together, these data suggest that WEHI-3 cells exert anti-adipogenic effects and that both ROCKII and β-catenin are involved in this process.