» Articles » PMID: 31480347

Wnt10b Participates in Regulating Fatty Acid Synthesis in the Muscle of Zebrafish

Overview
Journal Cells
Publisher MDPI
Date 2019 Sep 5
PMID 31480347
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

There are 19 Wnt genes in mammals that belong to 12 subfamilies. Wnt signaling pathways participate in regulating numerous homeostatic and developmental processes in animals. However, the function of Wnt10b in fatty acid synthesis remains unclear in fish species. In the present study, we uncovered the role of the Wnt10b signaling pathway in the regulation of fatty acid synthesis in the muscle of zebrafish. The gene of Wnt10b was overexpressed in the muscle of zebrafish using pEGFP-N1-Wnt10b vector injection, which significantly decreased the expression of glycogen synthase kinase 3β (GSK-3β), but increased the expression of β-catenin, peroxisome proliferators-activated receptor γ (PPARγ), and CCAAT/enhancer binding protein α (C/EBPα). Moreover, the activity and mRNA expression of key lipogenic enzymes ATP-citrate lyase (ACL), acetyl-CoA carboxylase (ACC) and fatty acid synthetase (FAS), and the content of non-esterified fatty acids (NEFA), total cholesterol (TC), and triglyceride (TG) were also significantly decreased. Furthermore, interference of the Wnt10b gene significantly inhibited the expression of β-catenin, PPARγ, and C/EBPα, but significantly induced the expression of GSK-3β, FAS, ACC, and ACL. The content of NEFA, TC, and TG as well as the activity of FAS, ACC, and ACL significantly increased. Thus, our results showed that Wnt10b participates in regulating fatty acid synthesis via β-catenin, C/EBPα and PPARγ in the muscle of zebrafish.

Citing Articles

Genomic context determines the effect of DNA methylation on gene expression in the gut epithelium of Atlantic salmon ().

Katirtzoglou A, Hansen S, Sveier H, Martin M, Brealey J, Limborg M Epigenetics. 2024; 19(1):2392049.

PMID: 39151124 PMC: 11332636. DOI: 10.1080/15592294.2024.2392049.


Artesunate targets cellular metabolism to regulate the Th17/Treg cell balance.

Chen K, Tang L, Nong X Inflamm Res. 2023; 72(5):1037-1050.

PMID: 37024544 DOI: 10.1007/s00011-023-01729-9.


The role of WNT10B in physiology and disease: A 10-year update.

Perkins R, Singh R, Abell A, Krum S, Miranda-Carboni G Front Cell Dev Biol. 2023; 11:1120365.

PMID: 36814601 PMC: 9939717. DOI: 10.3389/fcell.2023.1120365.


Dietary iron affects lipid deposition, nutritional element, and muscle quality in coho salmon ().

Liu D, Li L, Shan L, Zhang Q, Yu H Food Chem X. 2022; 15:100405.

PMID: 36211723 PMC: 9532727. DOI: 10.1016/j.fochx.2022.100405.


Effects of SPARCL1 on the proliferation and differentiation of sheep preadipocytes.

Xiao C, Jin H, Zhang L, Liu J, He M, Ma H Adipocyte. 2021; 10(1):658-669.

PMID: 34872433 PMC: 8654481. DOI: 10.1080/21623945.2021.2010901.

References
1.
Hansen E, Fernandes K, Goldspink G, Butterworth P, Umeda P, Chang K . Strong expression of foreign genes following direct injection into fish muscle. FEBS Lett. 1991; 290(1-2):73-6. DOI: 10.1016/0014-5793(91)81229-2. View

2.
Ridgeway A, Petropoulos H, Wilton S, Skerjanc I . Wnt signaling regulates the function of MyoD and myogenin. J Biol Chem. 2000; 275(42):32398-405. DOI: 10.1074/jbc.M004349200. View

3.
Doble B, Woodgett J . GSK-3: tricks of the trade for a multi-tasking kinase. J Cell Sci. 2003; 116(Pt 7):1175-86. PMC: 3006448. DOI: 10.1242/jcs.00384. View

4.
Cossu G, Borello U . Wnt signaling and the activation of myogenesis in mammals. EMBO J. 1999; 18(24):6867-72. PMC: 1171749. DOI: 10.1093/emboj/18.24.6867. View

5.
Farmer S . Transcriptional control of adipocyte formation. Cell Metab. 2006; 4(4):263-73. PMC: 1958996. DOI: 10.1016/j.cmet.2006.07.001. View