98%
921
2 minutes
20
Purpose: Juxtaposed with another zinc finger gene 1 (JAZF1) is known to be involved in various biological processes, including gluconeogenesis, insulin sensitivity, cell differentiation, lipid metabolism, and inflammation. However, its role in spontaneous preterm birth (SPTB) remains unclear.
Patients And Methods: We investigated the expression of JAZF1 mRNA using quantitative reverse transcription-PCR (qRT-PCR) in the decidual tissue of patients with SPTB compared to non-spontaneous preterm birth(non-SPTB). We also utilized Western blotting and ELISA to assess JAZF1 expression in peripheral blood from SPTB and non-SPTB patients. To further explore JAZF1's role, we validated the findings by constructing both knockdown and overexpression cellular models. The apoptosis level of decidual cells was detected by flow cytometry, and Western blotting was used to measure the expression of BCL-2, BAX, IκBα, phosphorylated IκBα, and COX-2. All collected data were statistically analyzed using GraphPad Prism 9.0. Gestational age was determined by crown-rump length (CRL) measured at 11-13 weeks. We compared the means between the two sample groups using either the independent sample t-test or the Wilcoxon rank-sum test, depending on the data distribution.
Results: The JAZF1 expression in peripheral blood and decidual tissue of SPTB patients was significantly lower than that in non-SPTB patients. Moreover, the level of apoptosis in decidual stromal cells was notably higher in SPTB. JAZF1 knockdown significantly reduced decidual stromal cells' migration and invasion capabilities while promoting apoptosis, additionally, knocking down JAZF1 in decidual stromal cells elevated Bax expression and the phosphorylation of IκBα, decreasing BCL-2 expression, further promotes the release of factors associated with uterine contractions, while contrasting outcomes were observed in the overexpression experiment.
Conclusion: The identification of JAZF1 as a reliable molecular marker for spontaneous preterm labor offers novel insights for developing early warning biomarkers or targeted therapies.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12382285 | PMC |
http://dx.doi.org/10.1186/s12884-025-07983-5 | DOI Listing |
Proc Natl Acad Sci U S A
September 2025
Department of Biomedical Engineering, University of Connecticut Health, Farmington, CT 06030.
Coopetition is a term from game theory that describes a mix of cooperative and competitive behavior. The maternal-fetal interface (MFI) among eutherian mammals presents close interaction of two distinct individuals. These interactions have resulted in a remarkable diversity in MFI structure, often interpreted as the outcome of maternal-fetal conflict.
View Article and Find Full Text PDFFASEB J
September 2025
Department of Obstetrics, Gynecology and Women's Health, University of Missouri School of Medicine, Columbia, Missouri, USA.
Ovarian steroid hormones-estrogen and progesterone-play a central role in regulating epithelial-stromal interactions in the uterus. These interactions are critical for uterine function, including endometrial receptivity, implantation, and decidualization. These interactions involve complex signaling crosstalk between the uterine epithelium and the underlying stroma, with dynamic cell population-specific roles.
View Article and Find Full Text PDFThe placenta is a complex organ with multiple immune and non-immune cell types that promote fetal tolerance and facilitate the transfer of nutrients and oxygen. The nonhuman primate (NHP) is a key experimental model for studying human pregnancy complications, in part due to similarities in placental structure, which makes it essential to understand how single-cell populations compare across the human and NHP maternal-fetal interface. We constructed a single-cell RNA-Seq (scRNA-Seq) atlas of the placenta from the pigtail macaque ( ) in the third trimester, comprising three different tissues at the maternal-fetal interface: the chorionic villi (placental disc), chorioamniotic membranes, and the maternal decidua.
View Article and Find Full Text PDFThe human endometrium is a dynamic tissue that lines the uterus and undergoes constant remodeling, making it especially susceptible to gynecological diseases like endometriosis and endometrial cancer. The molecular mechanisms of these conditions are not well understood, partly due to the lack of in vitro models that mimic endometrial physiology, which limits options for targeted intervention and treatment of these diseases. Mouse models are also inadequate, as common laboratory strains do not naturally undergo a menstrual cycle comparable to that of humans.
View Article and Find Full Text PDFBiol Reprod
September 2025
Center for Drug Discovery, Baylor College of Medicine, Houston, Texas 77030, USA.
Decidualization is the transformation of endometrial stromal cells into functionally specialized cells during the early stages of pregnancy. Occurring in mammals that develop invasive hemochorial placentae, decidualization is a pivotal evolutionary adaptation in mammals that supports pregnancy establishment, implantation, and placentation in a limited number of animal species. During decidualization, an endometrial stromal cell undergoes profound genetic, epigenetic, and proteomic changes, allowing it to prevent immunological rejection and fostering the development of a newly implanted embryo.
View Article and Find Full Text PDF