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Suppression of maturation of megakaryocyte colony forming unit in vitro by a platelet-released glycoprotein
Abstract:
The suppressive role of platelets on the growth of human marrow megakaryocyte colony forming units (CFU-M) in vitro was investigated by the use of a plasma clot assay. An inverse correlation was established between the number of megakaryocytic colonies grown and the platelet concentration of the plasma or the resultant serum used in the culture system. The suppressive effect of platelets on megakaryocyte colony formation reached a plateau at normal human blood platelet concentration and was specific for CFU-M growth, since marrow cell erythroid burst formation (BFU-E) and granulocytic-monocytic colony formation (CFU-GM) remained unaffected. The inhibitory activity was detectable in the supernatants of platelet suspensions aggregated by thrombin or ADP, and the inhibitory activity released from ADP-stimulated platelets was blocked by pretreatment of platelets with monoclonal antibody HuPl-m1. Partial purification of this activity was achieved by diethylaminoethyl (DEAE)-ion exchange and phytohemagglutinin (PHA)-E agarose affinity chromatography. This inhibitor is a glycoprotein with a molecular weight of 12-17K daltons. This platelet released glycoprotein does not affect the early proliferative phase of CFU-M in vitro but acts on a day 6-8 CFU-M-derived cell by adversely affecting its maturation into recognizable megakaryocytes. These findings demonstrate that a glycoprotein released from platelets suppresses the maturation of CFU-M into megakaryocytes.
Insights
Platelets release a glycoprotein that suppresses human megakaryocyte maturation. This finding is specific to megakaryocyte colony-forming units (CFU-M) and does not impact other blood cell growth.
Area of Science:
- Hematology
- Cell Biology
- Biochemistry
Background:
- Platelets play a complex role in hematopoiesis.
- Megakaryocytes are essential for platelet production.
- Understanding megakaryopoiesis regulation is crucial for blood disorders.
Purpose of the Study:
- To investigate the suppressive role of platelets on human marrow megakaryocyte colony-forming units (CFU-M) in vitro.
- To identify the specific mechanism and nature of platelet-derived inhibitors of megakaryopoiesis.
Main Methods:
- Plasma clot assay to assess CFU-M growth.
- Platelet aggregation with thrombin or ADP.
- Monoclonal antibody (HuPl-m1) inhibition assay.
- DEAE-ion exchange and PHA-E agarose chromatography for purification.
- Molecular weight determination.
Main Results:
- Platelet concentration inversely correlated with CFU-M growth.
- Suppressive effect plateaued at normal platelet levels and was specific to CFU-M.
- Inhibitory activity released from aggregated platelets.
- Purified inhibitor is a 12-17K dalton glycoprotein.
- Glycoprotein inhibits megakaryocyte maturation, not proliferation.
Conclusions:
- Platelets release a glycoprotein that specifically suppresses megakaryocyte maturation.
- This platelet-derived factor acts on later-stage CFU-M-derived cells.
- Findings elucidate a novel regulatory mechanism in megakaryopoiesis.