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Updated: Oct 1, 2026

Generation of Lymphocytic Microparticles and Detection of their Proapoptotic Effect on Airway Epithelial Cells
Published on: February 20, 2015
Platelet-derived microparticles stimulate proliferation, survival, adhesion, and chemotaxis of hematopoietic cells
Monika Baj-Krzyworzeka1, Marcin Majka, Domenico Pratico
1Stem Cell Biology Program, James Graham Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.
Objective:
Peripheral blood platelet-derived microparticles (PMPs) circulate in blood and may interact directly with target cells affecting their various biological functions.
Methods:
To investigate the effect of human PMPs on hematopoiesis, we first phenotyped them for expression of various surface molecules and subsequently studied various biological responses of normal stem/progenitor (CD34(+)) and more differentiated precursor cells as well as several leukemic cell lines to PMPs.
Results:
We found that, in addition to platelet-endothelium attachment receptors (CD41, CD61 and CD62), PMPs express G-protein-coupled seven transmembrane-span receptors such as CXCR4 and PAR-1; cytokine receptors including TNF-RI, TNF-RII, and CD95; and ligands such as CD40L and PF-4. Moreover, we found that several of these receptors could be transferred by PMPs to the membranes of normal as well as malignant cells and observed that PMPs: 1) chemoattract these cells, 2) increase their adhesion, proliferation, and survival, and 3) activate in these cells various intracellular signaling cascades including MAPK p42/44, PI-3K-AKT, and STAT proteins. The biological effects of PMPs were only partly reduced by heat inactivation or trypsin digest, indicating that, in addition to the protein components of PMPs, lipid components are also responsible for their biological activity.
Conclusions:
We conclude that PMPs modulate biological functions of hematopoietic cells and postulate that they play an important but as yet not fully understood role in intercellular cross-talk in hematopoiesis. Further studies, however, are needed to identify the PMP components that exert specific biological effects.
Insights
Peripheral blood microparticles (PMPs) influence hematopoietic cell functions by transferring surface receptors. These PMPs chemoattract, increase adhesion, proliferation, and survival, impacting intercellular communication in hematopoiesis.
Area of Science:
- Hematology
- Cell Biology
- Molecular Biology
Background:
- Peripheral blood platelet-derived microparticles (PMPs) are circulating vesicles with potential to influence cellular functions.
- Understanding PMP interactions with hematopoietic cells is crucial for comprehending hematopoiesis.
Purpose of the Study:
- To investigate the effects of human PMPs on normal and malignant hematopoietic cells.
- To characterize the surface molecules of PMPs and their role in cellular responses.
Main Methods:
- Phenotyping of PMPs for surface molecule expression.
- Assessing biological responses of CD34(+) stem/progenitor cells, precursor cells, and leukemic cell lines to PMPs.
- Investigating intracellular signaling pathways activated by PMPs.
Main Results:
- PMPs express various receptors including CXCR4, PAR-1, TNF receptors, CD95, CD40L, and PF-4.
- PMPs transfer receptors to target cells, leading to chemoattraction, increased adhesion, proliferation, and survival.
- PMPs activate intracellular signaling cascades (MAPK, PI-3K-AKT, STAT) in target cells; both protein and lipid components contribute to their activity.
Conclusions:
- PMPs modulate biological functions of hematopoietic cells, suggesting a significant role in intercellular cross-talk.
- Further research is required to identify specific PMP components responsible for distinct biological effects.
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