Neuropeptide B promotes differentiation of rodent white preadipocytes into mature adipocytes

被引:1
作者
Wojciechowicz, T. [1 ]
Szczepankiewicz, D. [1 ]
Strowski, M. Z. [2 ,3 ]
Nowak, K. W. [1 ]
Skrzypski, M. [1 ]
机构
[1] Poznan Univ Life Sci, Dept Anim Physiol Biochem & Biostruct, PL-60637 Poznan, Poland
[2] Charite Univ Med Berlin, Dept Hepatol & Gastroenterol, D-13353 Berlin, Germany
[3] Med Clin III, D-15236 Frankfurt, Oder, Germany
关键词
Adipocytes; Adipogenesis; Differentiation; Neuropeptide B; Preadipocytes; Proliferation; Rat; COUPLED RECEPTORS GPR7; IDENTIFICATION; ADIPOGENESIS; SECRETION; LIPOLYSIS; LIGANDS; LEPTIN;
D O I
10.1016/j.mce.2023.111850
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neuropeptide B (NPB) modulates energy homeostasis and metabolism through activation of NPBWR1 and NPBWR2 in humans and NPBWR1 in rodents. Recently, we reported that NPB promotes adipogenesis in rat brown preadipocytes. In the present study, we evaluated the effects of NPB on proliferation and differentiation into mature adipocytes of white rat preadipocytes and 3T3-L1 cells. We found the expression of NPBWR1 and NPB on mRNA and protein level in rat white preadipocytes and 3T3-L1 cells. NPB increased expression of mRNA and protein production of adipogenic genes (PPAR gamma, C/EBPS, CEBP alpha and FABP4) in rat preadipocytes and 3T3-L1 cells during the differentiation process. Furthermore, NPB stimulated lipid accumulation in rat preadipocytes and 3T3-L1 cells. In addition, we found that NPB promotes phosphorylation of p38 kinase in rat preadipocytes and 3T3-L1 cells. NPB failed to stimulate expression of proadipogenic genes in the presence of p38 inhibitor. NPB failed to modulate viability and proliferation of rat preadipocytes and 3T3-L1 cells. Taken together, we report that NPB promotes differentiation of rodent preadipocytes via p38-dependent mechanism. NPB does not modulate viability and proliferation of rat preadipocytes and 3T3-L1 cells.
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页数:10
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