Document Type

Article

Major

Molecular & Cell Biology

Mentor

Prof. Vanessa Scanlon, Center for Regenerative Medicine and Skeletal Biology

Disciplines

Cell and Developmental Biology | Life Sciences

Abstract

The human bone marrow is a complex microenvironment comprised of hematopoietic, stromal, and bone marrow endothelial cells (BMECs). This study builds on previous findings to explore the regulatory role of BMECs in influencing the expansion and lineage choice of megakaryocytic-erythroid progenitors (MEPs). Understanding these interactions has the potential to advance transfusion medicine and improve treatments for conditions like thrombocytopenia and anemia. Due to complications with isolating human BMEC, we transitioned to a murine model. Murine BMECs were isolated and magnetic cell separation was employed to enrich for endothelial cells (ECs), which were then cultured over a 20-day period using standard techniques. We tested the functional consequences on primary MEP fate using flow cytometry and co-cultured colony-forming unit (CFU) assays. Microscopy confirmed BMEC morphology and flow cytometry confirmed the successful isolation of murine BMECs by detecting specific endothelial cell markers. The CFU assay plates have been completed but remain to be scanned; results are still pending. Despite the challenges faced, this study provides unique and valuable insights into BMEC-MEP interactions. Future research will aim to address technical difficulties encountered and analyze the CFU data once the imaging resources are restored. The findings contribute to ongoing BMEC transplantation research and the development of in vitro systems for improving blood product generation in transfusion medicine.

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