Journalartikel

Perinatal Obesity Induces Hepatic Growth Restriction with Increased DNA Damage Response, Senescence, and Dysregulated Igf-1-Akt-Foxo1 Signaling in Male Offspring of Obese Mice


AutorenlisteKasper, Philipp; Selle, Jaco; Vohlen, Christina; Wilke, Rebecca; Kuiper-Makris, Celien; Klymenko, Oleksiy; Bae-Gartz, Inga; Schoemig, Charlotte; Quaas, Alexander; Schumacher, Bjorn; Demir, Munevver; Buerger, Martin; Lang, Sonja; Martin, Anna; Steffen, Hans-Michael; Goeser, Tobias; Doetsch, Jorg; Alcazar, Miguel A. Alejandre

Jahr der Veröffentlichung2022

ZeitschriftInternational Journal of Molecular Sciences

Bandnummer23

Heftnummer10

eISSN1422-0067

Open Access StatusGold

DOI Linkhttps://doi.org/10.3390/ijms23105609

VerlagMDPI


Abstract
Maternal obesity predisposes for hepato-metabolic disorders early in life. However, the underlying mechanisms causing early onset dysfunction of the liver and metabolism remain elusive. Since obesity is associated with subacute chronic inflammation and accelerated aging, we test the hypothesis whether maternal obesity induces aging processes in the developing liver and determines thereby hepatic growth. To this end, maternal obesity was induced with high-fat diet (HFD) in C57BL/6N mice and male offspring were studied at the end of the lactation [postnatal day 21 (P21)]. Maternal obesity induced an obese body composition with metabolic inflammation and a marked hepatic growth restriction in the male offspring at P21. Proteomic and molecular analyses revealed three interrelated mechanisms that might account for the impaired hepatic growth pattern, indicating prematurely induced aging processes: (1) Increased DNA damage response (gamma H2AX), (2) significant upregulation of hepatocellular senescence markers (Cdnk1a, Cdkn2a); and (3) inhibition of hepatic insulin/insulin-like growth factor (IGF)-1-AKT-p38-FoxO1 signaling with an insufficient proliferative growth response. In conclusion, our murine data demonstrate that perinatal obesity induces an obese body composition in male offspring with hepatic growth restriction through a possible premature hepatic aging that is indicated by a pathologic sequence of inflammation, DNA damage, senescence, and signs of a possibly insufficient regenerative capacity.



Zitierstile

Harvard-ZitierstilKasper, P., Selle, J., Vohlen, C., Wilke, R., Kuiper-Makris, C., Klymenko, O., et al. (2022) Perinatal Obesity Induces Hepatic Growth Restriction with Increased DNA Damage Response, Senescence, and Dysregulated Igf-1-Akt-Foxo1 Signaling in Male Offspring of Obese Mice, International Journal of Molecular Sciences, 23(10), Article 5609. https://doi.org/10.3390/ijms23105609

APA-ZitierstilKasper, P., Selle, J., Vohlen, C., Wilke, R., Kuiper-Makris, C., Klymenko, O., Bae-Gartz, I., Schoemig, C., Quaas, A., Schumacher, B., Demir, M., Buerger, M., Lang, S., Martin, A., Steffen, H., Goeser, T., Doetsch, J., & Alcazar, M. (2022). Perinatal Obesity Induces Hepatic Growth Restriction with Increased DNA Damage Response, Senescence, and Dysregulated Igf-1-Akt-Foxo1 Signaling in Male Offspring of Obese Mice. International Journal of Molecular Sciences. 23(10), Article 5609. https://doi.org/10.3390/ijms23105609



Schlagwörter


CELLULAR SENESCENCELIVER-REGENERATIONMATERNAL OBESITYmetabolic programming

Zuletzt aktualisiert 2025-10-06 um 11:40