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Updated: Aug 19, 2026

Isolation of Precursor B-cell Subsets from Umbilical Cord Blood
Published on: April 16, 2013
The common myelolymphoid progenitor: a key intermediate stage in hemopoiesis generating T and B cells
Min Lu1, Hiroshi Kawamoto, Yoshihiro Katsube
1Department of Immunology, Institute for Frontier Medical Sciences, Kyoto University, Sakyo-ku, Kyoto, Japan.
Abstract:
We have previously shown that the common progenitors for myeloid, T, and B cell lineages are enriched in the earliest population of murine fetal liver. However, it remained unclear whether such multipotent progenitors represent the pluripotent progenitors capable of generating all hemopoietic cells or they also comprise progenitors restricted to myeloid, T, and B cell lineages. To address this issue, we have developed a new clonal assay covering myeloid, erythroid, T, and B cell lineages, and using this assay the developmental potential of individual cells in subpopulations of lineage marker-negative (Lin(-)) c-kit(+) murine fetal liver cells was investigated. We identified the progenitor generating myeloid, T, and B cells, but not erythroid cells in the Sca-1(high) subpopulation of Lin(-)c-kit(+) cells that can thus be designated as the common myelolymphoid progenitor (CMLP). Common myeloerythroid progenitors were also detected. These findings strongly suggest that the first branching point in fetal hemopoiesis is between the CMLP and common myeloerythroid progenitors. T and B cell progenitors may be derived from the CMLP through the previously identified myeloid/T and myeloid/B bipotent stages, respectively.
Insights
Researchers identified the common myelolymphoid progenitor (CMLP) in murine fetal liver. This progenitor generates myeloid, T, and B cells, clarifying early hematopoietic branching points.
Area of Science:
- Hematopoiesis
- Developmental Biology
- Immunology
Background:
- Common progenitors for myeloid, T, and B cells are found in early murine fetal liver.
- The precise developmental potential of these multipotent progenitors remained unclear.
Purpose of the Study:
- To investigate the developmental potential of individual cells within murine fetal liver subpopulations.
- To clarify whether multipotent progenitors are pluripotent or lineage-restricted.
Main Methods:
- Development of a novel clonal assay covering myeloid, erythroid, T, and B cell lineages.
- Analysis of subpopulations within lineage marker-negative (Lin(-)) c-kit(+) murine fetal liver cells.
Main Results:
- Identification of the common myelolymphoid progenitor (CMLP) within the Sca-1(high) subpopulation.
- CMLP generates myeloid, T, and B cells but not erythroid cells.
- Detection of common myeloerythroid progenitors.
Conclusions:
- The first branching point in fetal hematopoiesis occurs between CMLP and common myeloerythroid progenitors.
- T and B cell progenitors likely arise from CMLP via intermediate bipotent stages.
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