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Published on: July 29, 2018
Derivation of multipotent progenitors from human circulating CD14+ monocytes
Noriyuki Seta1, Masataka Kuwana
1Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Experimental Hematology
|April 6, 2010
Summary
Circulating monocytes are more versatile than previously believed, giving rise to multipotent cells (MOMCs) capable of tissue repair and regeneration. These findings expand our understanding of monocyte functions beyond immunity.
Area of Science:
- * Stem Cell Biology
- * Immunology
- * Regenerative Medicine
Background:
- * Circulating CD14(+) monocytes are considered precursors for phagocytes like macrophages.
- * A novel primitive cell population, monocyte-derived multipotential cells (MOMCs), was recently identified.
- * The circulating precursors for MOMCs remained undetermined.
Purpose of the Study:
- * To identify the circulating precursors for MOMCs.
- * To characterize the differentiation potential of MOMCs.
- * To explore the role of MOMCs in tissue repair and hematopoiesis.
Main Methods:
- * Comparative gene expression profiling of MOMCs and other monocyte-derived cells.
- * In vitro culture of MOMCs requiring fibronectin and platelet-derived factors.
- * Analysis of MOMC differentiation capacity into various non-phagocytic cell types.
- * Assessment of MOMCs' ability to promote hematopoietic progenitor cell expansion.
Main Results:
- * MOMCs express embryonic stem cell markers Nanog and Oct-4.
- * MOMCs differentiate into diverse cell types including bone, cartilage, muscle, neurons, and endothelium.
- * MOMCs support ex vivo expansion of hematopoietic progenitor cells.
- * Circulating monocytes are more multipotent than previously recognized.
Conclusions:
- * Circulating CD14(+) monocytes can differentiate into MOMCs, which possess multipotent progenitor capacity.
- * MOMCs contribute to tissue repair and regeneration beyond immune responses.
- * Monocytes play a broader role in physiology, including tissue repair and hematopoiesis.
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