bioRxiv Science⌕ Search

Biology subjects

Podinic, T.

Publications and source records attributed to Podinic, T..

3 recordsLinked to original sources

Defining a hypoxic exposure paradigm for modelling preeclampsia-associated syncytiotrophoblast dysfunction in human blastocyst-derived placental stem cells

Introduction: Preeclampsia (PE) is a hypertensive pregnancy disorder in which placental dysfunction is thought to play a central role. Although hypoxia is widely used to model PE-associated syncytiotrophoblast (ST) dysfunction in vitro, considerable variability in oxygen control conditions and hypoxic exposure paradigms has limited standardization across studies. This study aimed to establish physiologically relevant oxygen control conditions and identify a hypoxic exposure paradigm that consistently recapitulates characteristic features of PE-associated ST dysfunction. Methods: Human blastocyst-derived trophoblast stem cells were differentiated into STs and exposed to physiological (8% O2), atmospheric (21% O2), or hypoxic (1% O2) conditions for 24 or 48 h. Angiogenic and apoptotic marker expression, cell death, and mitochondrial stress were assessed. Results: Compared with atmospheric oxygen, 8% O2 reduced cell death and more closely reflected physiological ST conditions. Acute hypoxia (24 h) induced a robust PE-like phenotype in STs characterized by induction of anti-angiogenic markers, sFlt-1 and sEng, reduced expression of the pro-angiogenic factor PlGF, and increased cell death, apoptotic signalling and mitochondrial stress. Notably, induction of several of these markers was attenuated or reversed following prolonged hypoxic exposure. Conclusions: These findings identify 8% O2 as a physiologically relevant control condition for modelling PE-associated ST dysfunction relative to 21% O2, and demonstrate that 24 h of severe hypoxia more consistently reproduces key molecular and cellular features of PE than prolonged hypoxia. This work establishes a framework for modelling hypoxia-induced ST dysfunction while highlighting the importance of oxygen control conditions and hypoxic exposure duration when modeling PE in vitro.

cell biology↗

Placental transcriptomics reveals alterations in metabolic and transport gene programs following prenatal cannabis smoke exposure

Background: Prenatal cannabis use is increasing, yet the effects of inhaled cannabis smoke on placental molecular function remain poorly defined. Objective: To characterize placental transcriptomic alterations following prenatal cannabis smoke exposure using a physiologically relevant murine inhalation model. Methods: Timed-pregnant CD-1 mice were exposed to cannabis cigarette smoke or room air from embryonic day (E)6.5 to 18.5. Placentae were collected at E18.5 for microarray-based transcriptomic profiling. Differential gene expression was assessed using fetal sex adjusted linear models and false discovery rate correction. Gene set variation and ranked pathway enrichment were performed to evaluate compartment-associated and biological transcriptional programs. Selected genes were validated by quantitative PCR. Results: Large-scale transcriptomic profiles revealed no clear visual clustering by exposure; however, 23 genes were differentially expressed (FDR <0.05, |log2 fold change| > 0.5). Labyrinth-associated transcriptional signatures were reduced, whereas junctional-associated signatures were increased in exposed placentae. Pathway analyses revealed negative enrichment of fatty acid metabolism, bioenergetic, and transmembrane transport pathways, alongside positive enrichment of RNA processing and transcriptional-regulatory pathways. Quantitative PCR confirmed altered expression of multiple transport-related genes. Electron transport chain-associated gene expression was altered despite preserved placental respiratory measurements. Conclusions: Prenatal cannabis smoke exposure is associated with subtle yet coordinated placental transcriptional alterations involving metabolic, transport-associated, and gene-regulatory pathways, alongside compartment-associated transcriptional shifts. These findings provide insight into placental responses to whole cannabis smoke exposure and identify pathways that may contribute to altered placental function during pregnancy.

physiology↗

Prenatal cannabis smoke exposure alters placental development in a murine model of pregnancy

Cannabis use during pregnancy continues to increase with smoking remaining the most common mode of consumption. While clinical studies highlight an association between prenatal cannabis use and adverse pregnancy outcomes, less is known about placental outcomes, even though many of the reported pregnancy outcomes are thought to be mediated via placental dysfunction. Here, we established a mouse model of gestational cannabis smoke exposure to investigate the impacts on fetal outcomes and placental structure and function. Pregnant CD1 mice were exposed daily to {Delta}9-tetrahydrocannabinol (THC)-dominant cannabis smoke (12-14% THC, 0-2% CBD) or filtered air from embryonic day (E)6.5 to E18.5 or parturition. Cannabinoid analyses in cannabis smoke-exposed, paired maternal and fetal livers revealed total THC and 11-Nor-9-carboxy-THC (THCA) concentrations of 135.95 {+/-} 13.60 ng/g and 30.84 {+/-} 4.68 ng/g, respectively. Moreover, Cyp1a1, a smoke-inducible enzyme, was induced by 4-fold in cannabis smoke-exposed placentae. No changes in offspring body weights were observed; however, there was a marked decrease in the brain-to-body weight ratio of exposed postnatal day 1 (PND1) offspring. Placentae from exposed dams were significantly reduced in size, with altered zonation marked by a significantly decreased junctional zone and increased labyrinth zone. Key trophoblast differentiation markers (Tfap2c, Tpbpa, Pcdh12) and placental endocrine regulators (Pl2, Igf1r) were significantly downregulated following cannabis smoke exposure in placentas. Furthermore, transcript levels of placental nutrient and vascularization markers, Glut1, Vegfa and Pparg were significantly decreased in cannabis smoke-exposed placentas. By employing a physiologically relevant platform of prenatal cannabis exposure in vivo we demonstrate the adverse effects of prenatal cannabis smoke exposure on placental structure and function as well as on fetal brain growth.

physiology↗