» Articles » PMID: 29180630

ATF4 Overexpression Induces Early Onset of Hyperlipidaemia and Hepatic Steatosis and Enhances Adipogenesis in Zebrafish

Overview
Journal Sci Rep
Specialty Science
Date 2017 Nov 29
PMID 29180630
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

Activating transcription factor 4 (ATF4) is constitutively expressed in a variety of tissues, and regulates several pathological features associated with metabolic diseases such as non-alcoholic fatty liver diseases (NAFLD) and obesity. However, the role of ATF4 in animal model systems is poorly understood. To investigate ATF4 functions in zebrafish, we conditionally expressed ATF4 proteins, using a Tet-off transgenic system. We observed early-onset hyperlipidaemia and liver steatosis in ATF4 transgenic zebrafish (ATs) without doxycycline treatment (ATs - Dox). Oil Red O (ORO)-stained signals were predominant in the intravascular blood vessels and liver buds of larval ATs - Dox, indicating that ATF4 functionally promotes lipogenesis. Further, ATF4 overexpression accompanied the stimulation of the unfolded protein response. Therefore, adult ATs - Dox showed increased lipid accumulation, which led, in turn, to liver steatosis. Liver histology and ORO staining of ATs - Dox hepatocytes also indicated oxidative stress and induced NASH-like phenotypes. Moreover, ATF4 overexpression accelerated adipocyte differentiation via CCAAT enhancer binding protein-beta and peroxisome proliferator activated receptor-gamma inducible expression. ATs-Dox zebrafish showed increased weight gain with larger fat pads due to adipocyte hyperplasia. In this study, we report that ATF4 is a potential stimulator of lipid biosynthesis and adipogenesis in zebrafish.

Citing Articles

Impaired RelA signaling and lipid metabolism dysregulation in hepatocytes: driving forces in the progression of metabolic dysfunction-associated steatotic liver disease.

He Y, Jiang J, Ou L, Chen Y, Abudukeremu A, Chen G Cell Death Discov. 2025; 11(1):49.

PMID: 39910053 PMC: 11799324. DOI: 10.1038/s41420-025-02312-3.


Identification of the shared gene MXD3 signatures and biological mechanism in patients with hip pain and prostate cancer.

Huang L, Xie Y, Jiang S, Gong B, Feng Y, Shan H Medicine (Baltimore). 2024; 103(37):e39592.

PMID: 39287260 PMC: 11404923. DOI: 10.1097/MD.0000000000039592.


The Roles of White Adipose Tissue and Liver NADPH in Dietary Restriction-Induced Longevity.

Jamerson L, Bradshaw P Antioxidants (Basel). 2024; 13(7).

PMID: 39061889 PMC: 11273496. DOI: 10.3390/antiox13070820.


The tunicamycin derivative TunR2 exhibits potent antibiotic properties with low toxicity in an in vivo Mycobacterium marinum-zebrafish TB infection model.

Nonarath H, Jackson M, Penoske R, Zahrt T, Price N, Link B J Antibiot (Tokyo). 2024; 77(4):245-256.

PMID: 38238588 PMC: 11403873. DOI: 10.1038/s41429-023-00694-z.


Hugan Qingzhi tablets attenuates endoplasmic reticulum stress in nonalcoholic fatty liver disease rats by regulating PERK and ATF6 pathways.

Yang M, Yao X, Xia F, Xiang S, Tang W, Zhou B BMC Complement Med Ther. 2024; 24(1):36.

PMID: 38216941 PMC: 10785447. DOI: 10.1186/s12906-024-04336-1.


References
1.
Zheng Z, Zhang C, Zhang K . Measurement of ER stress response and inflammation in the mouse model of nonalcoholic fatty liver disease. Methods Enzymol. 2011; 489:329-48. DOI: 10.1016/B978-0-12-385116-1.00019-4. View

2.
Chen H, Yuan R, Zhang Y, Zhang X, Chen L, Zhou X . ATF4 regulates SREBP1c expression to control fatty acids synthesis in 3T3-L1 adipocytes differentiation. Biochim Biophys Acta. 2016; 1859(11):1459-1469. DOI: 10.1016/j.bbagrm.2016.07.010. View

3.
Cullinan S, Diehl J . Coordination of ER and oxidative stress signaling: the PERK/Nrf2 signaling pathway. Int J Biochem Cell Biol. 2005; 38(3):317-32. DOI: 10.1016/j.biocel.2005.09.018. View

4.
Zhu G, Ye R, Jung D, Barron E, Friedline R, Benoit V . GRP78 plays an essential role in adipogenesis and postnatal growth in mice. FASEB J. 2012; 27(3):955-64. PMC: 3574283. DOI: 10.1096/fj.12-213330. View

5.
Vallejo M, Ron D, Miller C, Habener J . C/ATF, a member of the activating transcription factor family of DNA-binding proteins, dimerizes with CAAT/enhancer-binding proteins and directs their binding to cAMP response elements. Proc Natl Acad Sci U S A. 1993; 90(10):4679-83. PMC: 46576. DOI: 10.1073/pnas.90.10.4679. View