Medizinische Universität Graz - Research portal

Logo MUG Resarch Portal

Selected Publication:

SHR Neuro Cancer Cardio Lipid Metab Microb

Hoch, D; Majali-Martinez, A; Bandres-Meriz, J; Bachbauer, M; Pöchlauer, C; Kaudela, T; Bankoglu, EE; Stopper, H; Glasner, A; Hauguel-de, Mouzon, S; Gauster, M; Tokic, S; Desoye, G.
Obesity-associated non-oxidative genotoxic stress alters trophoblast turnover in human first trimester placentas.
Mol Hum Reprod. 2024; gaae027 Doi: 10.1093/molehr/gaae027 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Leading authors Med Uni Graz
Hoch Denise
Tokic Silvija
Co-authors Med Uni Graz
Bachbauer Martina
Bandrés Mériz Julia
Desoye Gernot
Gauster Martin
Kaudela Theresa-Maria
Majali Martinez Alejandro
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
Placental growth is most rapid during the first trimester (FT) of pregnancy, making it vulnerable to metabolic and endocrine influences. Obesity, with its inflammatory and oxidative stress, can cause cellular damage. We hypothesized that maternal obesity increases DNA damage in the FT placenta, affecting DNA damage response and trophoblast turnover. Examining placental tissue from lean and obese non-smoking women (4-12 gestational weeks), we observed higher overall DNA damage in obesity (COMET assay). Specifically, DNA double-strand breaks were found in villous cytotrophoblasts (vCTB; semi-quantitative γH2AX immunostaining), while oxidative DNA modifications (8-OHdG; FPG-COMET assay) were absent. Increased DNA damage in obese FT placentas did not correlate with enhanced DNA damage sensing and repair. Indeed, obesity led to reduced expression of multiple DNA repair genes (mRNA array), which were further shown to be influenced by inflammation through in vitro experiments using TNFα treatment on FT chorionic villous explants. Tissue changes included elevated vCTB apoptosis (TUNEL assay; caspase-cleaved cytokeratin 18), but unchanged senescence (p16) and reduced proliferation (Ki67) of vCTB, the main driver of FT placental growth. Overall, obesity is linked to heightened non-oxidative DNA damage in FT placentas, negatively affecting trophoblast growth and potentially leading to temporary reduction in early fetal growth.

Find related publications in this database (Keywords)
placental growth
trophoblast
proliferation
apoptosis
senescence
early pregnancy
DNA damage response
© Med Uni GrazImprint