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PMID: 10641435 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Stochastic model revisited.

International journal of hematology ·Vol. 69 ·No. 1 ·1999-01-00 ·Pages 2-5

Ogawa M

Abstract

Micromanipulation of murine and human hematopoietic progenitors has demonstrated various combinations of lineages in multilineage colonies, a finding consistent with the stochastic model of stem cell differentiation. Debate continued, however, on the mechanisms of stem cell differentiation, partly because some studies of cell lines suggested a deterministic model. Recently, transfection of primary hematopoietic progenitors with natural or chimeric cytokine receptors demonstrated that forced expression of cytokine receptors does not change the intrinsic differentiation potential of the primary progenitors. Studies also have demonstrated remarkable absence of specificity of signaling pathways in the primary progenitors. These studies are consistent with the stochastic model of stem cell differentiation in which cytokines play permissive and not instructive roles. This review summarizes some of the pertinent literature and discusses the cellular and molecular mechanisms of stem cell differentiation.

MeSH Terms
Animals Cell Differentiation Hematopoiesis Hematopoietic Cell Growth Factors/physiology Hematopoietic Stem Cells/cytology,metabolism Humans Mice Receptors, Cytokine/physiology Signal Transduction Stochastic Processes
Chemicals
Hematopoietic Cell Growth Factors Receptors, Cytokine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Ogawa M
Department of Veterans Affairs Medical Center, Charleston, South Carolina, USA. ogawam@musc.edu
Article Info
Journal
International journal of hematology
Abbr.
Int J Hematol
ISSN
0925-5710
Published
1999-01-00
Pages
2-5
Language
English
Region
Japan
NLM ID
9111627
Subset
IM
Grants
NIDDK NIH HHS · R01 DK/HL 48714 · United States
NIDDK NIH HHS · R01 DK32294 · United States
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