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Embryonic stem cells (ESCs) exhibit unique attributes of boundless self-renewal and pluripotency, making them invaluable for fundamental investigations and clinical endeavors. Previous examinations of microgravity effects on ESC self-renewal and differentiation have predominantly maintained a descriptive nature, constrained by limited experimental opportunities and techniques. In this investigation, we present compelling evidence derived from murine and human ESCs, demonstrating that simulated microgravity (SMG)-induced stress significantly impacts self-renewal and pluripotency through a previously unidentified conserved mechanism. Specifically, SMG induces the upregulation of heat shock protein genes, subsequently enhancing the expression of core pluripotency factors and activating the Wnt and/or LIF/STAT3 signaling pathways, thereby fostering ESC self-renewal. Notably, heightened Wnt pathway activity, facilitated by Tbx3 upregulation, prompts mesoendodermal differentiation in both murine and human ESCs under SMG conditions. Recognizing potential disparities between terrestrial SMG simulations and authentic microgravity, forthcoming space flight experiments are imperative to validate the impact of reduced gravity on ESC self-renewal and differentiation mechanisms.
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http://dx.doi.org/10.1038/s41420-024-01846-2 | DOI Listing |
Math Biosci Eng
July 2025
Department of Mathematics and Statistics, University of New Brunswick, Fredericton, NB, Canada.
Intratumoural epigenetic heterogeneity, which affects the outcome of many cancer treatments, results from stem cell-differentiated cell hierarchy. Cancer stem cells, also known as tumour-initiating cells, are a pluripotent subpopulation of tumour cells capable of creating a tumour clone through self-renewal and differentiation. Oncolytic viral therapy is a category of cancer therapeutics with high specificity in targeting cancer cells while leaving normal cells unharmed.
View Article and Find Full Text PDFStem Cell Res Ther
September 2025
Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Department of Rheumatology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Background: Genomic studies have linked single nucleotide variants in the enhancer region of the leukemia inhibitory factor receptor (Lifr) gene to chromatin accessibility and the regulation of self-renewal in mouse embryonic stem cells (mESCs). However, the underlying mechanisms remain unclear. This study investigates the role of the transcription factor BTB and CNC homology 1 (BACH1) in regulating the Lifr enhancer and its impact on mESC pluripotency.
View Article and Find Full Text PDFStem Cell Res Ther
September 2025
Research Center for Animal Genetic Resources of Mongolia Plateau, College of Life Sciences, Inner Mongolia University, Hohhot, 010020, China.
Background: Argininosuccinate synthase (ASS1) is a pivotal enzyme involved in the urea cycle, playing a crucial role in aspartate catabolism, arginine and nitric oxide biosynthesis. These biological processes are crucial for the growth and development of mammals. However, the functions of urea cycle-related genes in mouse embryonic stem cells (mESCs) remain largely unclear.
View Article and Find Full Text PDFNaunyn Schmiedebergs Arch Pharmacol
September 2025
Department of Medical Genetics, School of Medicine, Yeditepe University, Istanbul, 34755, Turkey.
Chordoma is a rare, slow-growing malignancy of notochordal origin characterized by a high degree of chemoresistance and limited therapeutic responsiveness. Despite advances in molecular profiling, the mechanisms underlying its cellular plasticity and therapy evasion remain incompletely defined. Emerging evidence across solid tumors suggests that cancer stem-like cells (CSCs) and the epithelial-to-mesenchymal transition (EMT) play central roles in driving tumor progression, metastatic potential, and drug resistance.
View Article and Find Full Text PDFBiomaterials
August 2025
Center for Regeneration, Aging and Chronic Diseases, School of Basic Medical Sciences, Tsinghua University, Beijing, 100084, China; SXMU-Tsinghua Collaborative Center for Frontier Medicine, Taiyuan, Shanxi Province, 030001, China; State Key Laboratory for Complex, Severe and Rare Diseases, Tsinghua
Macrophages play critical roles in various physiological and pathological processes, yet their scalable production for therapeutic applications remains a challenge. Here, we present a porous microscaffold (PMS) that enables robust hematopoietic differentiation from human pluripotent stem cell (hPSC)-derived mesoderm. Within PMS, mesoderm cells self-organize into vascular structures reminiscent of the early aorta-gonad-mesonephros (AGM) niches, promoting efficient endothelial-to-hematopoietic transition with minimal cytokine supplementation.
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