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Clinically patients with thrombocytopenia are in urgent need of platelet transfusion, thus it is necessary to produce the platelets in large scale in vitro to meet the clinical needs. In this study, we developed efficient protocol to generate functioning platelets by differentiating umbilical cord blood (CB)-derived CD34 cells into mature megakaryocytes. Under our condition, up to 85% of mature megakaryocytes were generated from CB-derived CD34 cells, and over 75% CD42bCD62p platelets were produced. The megakaryocytes at day 12 after the differentiation had the similar gene expression pattern to natural mature megakaryocytes, and AMPK and insulin signal pathway were activated to inhibit the apoptosis and benefit platelet release. There were up to 72% of the platelets that could bind with PAC1, which is the highest rate of CB CD34 cell-derived platelets to play function to date. The recovery of hemostasis and coagulation was similar in thrombocytopenia mice injected with CB CD34 cell-derived platelets and with human blood-derived platelets, respectively, and it is the first time to demonstrate that human CB CD34 cell-derived platelets were functional . Therefore, our findings open a new avenue to provide an efficient approach to generate functional platelets for clinical applications.
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http://dx.doi.org/10.1089/scd.2024.0095 | DOI Listing |
Cell Signal
August 2025
Department of Infectious Diseases, Shengjing Hospital of China Medical University, Shenyang, China; Liaoning Key Laboratory of Viral Hepatitis, Shengjing Hospital of China Medical University, Shenyang, China. Electronic address:
Background And Aim: Hepatitis B virus (HBV) infection can lead to thrombocytopenia through its effects on hematopoiesis, although the underlying mechanisms have not been fully elucidated. Platelet production involves multiple stages, including the differentiation of mature megakaryocytes, which plays a pivotal role. In this study, we assessed the variances in megakaryocyte differentiation and maturation after HBV infection and investigated the molecular mechanism involved.
View Article and Find Full Text PDFThromb Res
August 2025
Department of Chemistry and Biochemistry, Université de Moncton, Moncton, New Brunswick, Canada; New Brunswick Center for Precision Medicine, Moncton, New Brunswick, Canada. Electronic address:
Megakaryocytes, a type of myeloid cell primarily produced in the bone marrow, are essential for releasing platelets into the bloodstream. Through platelet production, megakaryocytes transfer their own biological content to these cells, including inflammatory enzymes. Amongst these enzymes, 12-lipoxygenase (12-LO) has been shown to modulate platelet activation and is involved in several chronic inflammatory conditions.
View Article and Find Full Text PDFBiomedicines
July 2025
Department of Haematology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen 518000, China.
: Acute myeloid leukemia (AML) is a common and aggressive adults hematological malignancies. This study explored megakaryocyte-erythroid progenitors (MEPs) signature genes and constructed a prognostic model. : Uniform manifold approximation and projection (UMAP) identified distinct cell types, with differential analysis between AML-MEP and normal MEP groups.
View Article and Find Full Text PDFThe CBFA2T3::GLIS2 (CG) fusion protein causes aggressive pediatric acute megakaryoblastic leukemia (AMKL). Although dysregulated molecular pathways in AMKL have been identified, their role in early pre-leukemic transformation remains poorly understood. We developed a disease model utilizing genetically modified human induced pluripotent stem cells (hiPSC) physiologically and conditionally expressing CG.
View Article and Find Full Text PDFFront Cell Dev Biol
August 2025
Unité de Biologie Moléculaire, Cellulaire et du Développement (MCD, UMR 5077), Centre de Biologie Intégrative (CBI, FR 3743), Université de Toulouse, CNRS, UPS, Toulouse, France.
Invadosomes are a family of subcellular actin-based structures essential for cell-extracellular matrix (ECM) interaction and remodeling. In non-invasive cells, they are referred to as podosomes, which enable adhesion, migration, and ECM remodeling via secretion of metalloproteinases or mechano-traction. In invasive tumoral cells, these structures are called invadopodia due to their function.
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