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Updated: Feb 16, 2026

Isolation of Mouse Megakaryocyte Progenitors
Published on: May 20, 2021
A unique microenvironment in the developing liver supports the expansion of megakaryocyte progenitors
Nathalie Brouard1,2, Camille Jost1, Nadine Matthias2
1Université de Strasbourg, INSERM, Etablissement Français du Sang-Alsace, Biologie et Pharmacologie des Plaquettes Sanguines Unité Mixte de Recherche-S 949, Fédération de Médecine Translationnelle de Strasbourg, Strasbourg, France.
Insights
Researchers discovered a novel stromal cell population in the fetal liver that supports megakaryocyte production. This finding offers new insights into megakaryopoiesis and the fetal liver
Area of Science:
- Hematology
- Developmental Biology
- Stem Cell Biology
Background:
- The fetal liver is a critical site for hematopoietic stem cell (HSC) expansion.
- It is also a key organ for studying megakaryocyte progenitor differentiation.
Purpose of the Study:
- To identify and characterize novel stromal cell populations in the fetal liver involved in megakaryopoiesis.
- To investigate the role of these stromal cells in supporting megakaryocyte production from HSCs.
Main Methods:
- Flow cytometry was used to identify a specific stromal cell population (CD45-TER119-CD31-CD51+VCAM-1+PDGFRα-) in mouse fetal liver.
- Co-culture experiments were performed using this stromal population with mouse bone marrow HSCs and human HSC-myeloid progenitors.
- Megakaryocyte differentiation and proplatelet formation were assessed in vitro.
Main Results:
- A unique stromal cell population (V+P-) was identified in the fetal liver.
- This V+P- population efficiently supported megakaryocyte production from both mouse and human progenitors with limited cytokines.
- Co-cultured megakaryocytes were polyploid, expressed key markers (CD41/CD42c), and produced proplatelets, indicating functional maturity.
Conclusions:
- The fetal liver harbors a distinct cellular microenvironment crucial for megakaryopoiesis.
- The identified V+P- stromal cells play a significant role in supporting megakaryocyte development.
- This cellular niche presents a platform for discovering novel regulators of megakaryopoiesis.
Abstract:
The fetal liver is the site of a major expansion of the hematopoietic stem cell (HSC) pool and is also a privileged organ to study megakaryocyte progenitor differentiation. We identified in the mouse fetal liver at day 13.5 a discrete stromal cell population harboring a CD45-TER119-CD31-CD51+VCAM-1+PDGFRα- (V+P-) phenotype that lacked colony-forming unit fibroblast activity and harbored an hepatocyte progenitor signature. This previously undescribed V+P- population efficiently supported megakaryocyte production from mouse bone marrow HSC and human peripheral blood HSC-myeloid progenitors cultured in the presence of limited cytokine concentrations. Megakaryocytes obtained in V+P- cocultures were polyploid, positive for CD41/CD42c, and efficiently produced proplatelets. Megakaryocyte production appeared to be mediated by an expansion of the progenitor compartment through HSC-stromal cell contact. In conclusion, the fetal liver contains a unique cellular microenvironment that could represent a platform for the discovery of regulators of megakaryopoiesis.
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