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PMID: 7541305 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The long-term repopulating subset of hematopoietic stem cells is deterministic and isolatable by phenotype.

Immunity ·Vol. 1 ·No. 8 ·1994-11-00 ·Pages 661-73

Morrison SJ, Weissman IL

Abstract

The Thy-1.1loSca-1hiLin-/lo population, representing 0.05% of C57BL/Ka-Thy-1.1 bone marrow, is highly enriched for hematopoietic stem cells and includes all multipotent progenitors in this mouse strain; however, the functional reconstituting activity of this fraction is heterogeneous. Only around 25% of clonal reconstitutions by cells from this population are long term; remaining clones yield transient multilineage reconstitutions. By fractionating based on lineage marker expression, the Thy-1.1loSca-1hiLin-/lo population has been resolved into three subpopulations: Lin-Mac-1-CD4-; Lin-Mac-1loCD4-; and Mac-1loCD4lo. Of these, only the Lin-Mac-1-CD4- population is highly enriched for long-term reconstituting hematopoietic stem cells. A comparison of transient and long-term multipotent progenitors indicates that long-term progenitors have less CFU-S activity, are equally radioprotective, and are less frequently in cell cycle. The ability to predict the longevity of reconstitution based on lineage marker expression indicates that reconstitution potential is deterministic, not stochastic.

MeSH Terms
Animals Antigens, Differentiation/biosynthesis Bone Marrow Cells Bone Marrow Transplantation CD4 Antigens/analysis Colony-Forming Units Assay G2 Phase Hematopoiesis Hematopoietic Stem Cells/cytology Immunocompromised Host Leukocytes/cytology Lymphocyte Subsets/cytology Lymphocytes/cytology Macrophage-1 Antigen/analysis Mice Mice, Transgenic Peyer's Patches/cytology Proto-Oncogene Proteins/biosynthesis Proto-Oncogene Proteins c-kit Radiation Tolerance Receptor Protein-Tyrosine Kinases/biosynthesis Receptors, Colony-Stimulating Factor/biosynthesis Spleen/cytology Time Factors
Chemicals
Antigens, Differentiation CD4 Antigens Macrophage-1 Antigen Proto-Oncogene Proteins Receptors, Colony-Stimulating Factor Proto-Oncogene Proteins c-kit Receptor Protein-Tyrosine Kinases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Morrison S J
Department of Pathology, Stanford University School of Medicine, California 94305, USA.
Weissman I L
Article Info
Journal
Immunity
Abbr.
Immunity
ISSN
1074-7613
Published
1994-11-00
Pages
661-73
Language
English
Region
United States
NLM ID
9432918
Subset
IM
Grants
NCI NIH HHS · CA42551 · United States
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