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PMID: 12110174 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Myeloid or lymphoid promiscuity as a critical step in hematopoietic lineage commitment.

Developmental cell ·Vol. 3 ·No. 1 ·2002-07-00 ·Pages 137-47

Miyamoto T, Iwasaki H, Reizis B, Ye M, Graf T, Weissman IL, Akashi K

Abstract

We demonstrate here that "promiscuous" expression of myeloid or lymphoid genes precedes lineage commitment in hematopoiesis. Prospectively purified single common myeloid progenitors (CMPs) coexpress myelo-erythroid but not lymphoid genes, whereas single common lymphoid progenitors (CLPs) coexpress T and B lymphoid but not myeloid genes. Genes unrelated to the adopted lineage are downregulated in bipotent and monopotent descendants of CMPs and CLPs. Promiscuous gene expression does not alter the biological potential of multipotent progenitors: CMPs with an activated endogenous M lysozyme locus yield normal proportions of myelo-erythroid colonies, and CLPs expressing the pre-T cell receptor alpha gene differentiate into normal numbers of B cells. Thus, the accessibility for multiple myeloid or lymphoid programs promiscuously may allow flexibility in fate commitments at these multipotent stages.

MeSH Terms
Animals B-Lymphocytes/cytology,metabolism Bone Marrow/embryology,metabolism Cell Differentiation/genetics Cell Lineage/genetics Cells, Cultured Erythrocytes/cytology,metabolism Female Gene Expression Regulation, Developmental/physiology Genotype Hematopoiesis/genetics Hematopoietic Stem Cells/cytology,metabolism Lymphocytes/cytology,metabolism Male Megakaryocytes/cytology,metabolism Membrane Glycoproteins/genetics,metabolism Mice Mice, Mutant Strains Muramidase/genetics,metabolism Myeloid Cells/cytology,metabolism Proteins/genetics,metabolism Receptors, Antigen, T-Cell, alpha-beta T-Lymphocytes/cytology,metabolism Transcriptional Activation/physiology
Chemicals
Membrane Glycoproteins Proteins Receptors, Antigen, T-Cell, alpha-beta pre-T cell receptor alpha Muramidase
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Miyamoto Toshihiro
Departments of Pathology and Developmental Biology, Stanford University School of Medicine, Palo Alto, CA 94305, USA.
Iwasaki Hiromi
Reizis Boris
Ye Min
Graf Thomas
Weissman Irving L
Akashi Koichi
Article Info
Journal
Developmental cell
Abbr.
Dev Cell
ISSN
1534-5807
Published
2002-07-00
Pages
137-47
Language
English
Region
United States
NLM ID
101120028
Subset
IM
Grants
NIAID NIH HHS · AI47458 · United States
NCI NIH HHS · CA 86065 · United States
NIDDK NIH HHS · DK553074 · United States
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