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Simultaneous Study of the Recruitment of Monocyte Subpopulations Under Flow In Vitro
Published on: November 26, 2018
Production of tissue factor by monocyte progenitor cells
A C Stephens1, R Q Zheng, A R Russell
1Department of Paediatrics, St. Mary's Hospital, Paddington, London, UK.
Abstract:
Tissue factor (TF) is known to be produced by monocytes from human peripheral blood. However the production of this factor by haematopoietic progenitor cells is not yet known. We thus studied human monocyte progenitor cells isolated from bone marrow of normal and diseased individuals. These cells were non-adherent, monocytic and able to phagocytose particles ranging from 0.3-1 microns. Unactivated partial thromboplastin time clotting assay demonstrated procoagulant activity consistent with TF function, which was blocked by a neutralizing anti-TF monoclonal antibody, G12. The production of TF messenger RNA was demonstrated on dot blot and northern blot analysis utilizing an oligonucleotide probe.
Insights
Human monocyte progenitor cells from bone marrow produce tissue factor (TF). This finding reveals a new source of TF, crucial for understanding blood clotting and related diseases.
Area of Science:
- Hematology
- Immunology
- Molecular Biology
Background:
- Tissue factor (TF) is primarily known to be produced by monocytes in human peripheral blood.
- The production of TF by hematopoietic progenitor cells remains largely uncharacterized.
- Understanding TF production in early myeloid cells is critical for hemostasis and thrombosis research.
Purpose of the Study:
- To investigate the production of tissue factor (TF) by human monocyte progenitor cells.
- To determine if these progenitor cells exhibit procoagulant activity.
- To confirm the presence of TF and its messenger RNA (mRNA) in these cells.
Main Methods:
- Isolation of human monocyte progenitor cells from bone marrow of normal and diseased individuals.
- Characterization of cell properties including adherence and phagocytosis.
- Assessment of procoagulant activity using partial thromboplastin time clotting assays.
- Blocking of procoagulant activity with a neutralizing anti-TF monoclonal antibody (G12).
- Detection of TF mRNA using dot blot and northern blot analyses with an oligonucleotide probe.
Main Results:
- Isolated cells were non-adherent, monocytic, and capable of phagocytosis.
- Unactivated progenitor cells demonstrated procoagulant activity, indicative of TF function.
- This activity was specifically inhibited by the anti-TF monoclonal antibody G12.
- TF messenger RNA was successfully detected in these cells via molecular analyses.
Conclusions:
- Human monocyte progenitor cells isolated from bone marrow are capable of producing tissue factor (TF).
- These progenitor cells possess functional TF, contributing to procoagulant activity.
- The presence of TF mRNA confirms the synthesis of TF at the molecular level in these cells.
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