Literature DB >> 6124553

Hematopoietic stem cells with high proliferative potential. Assay of their concentration in marrow by the frequency and duration of cure of W/Wv mice.

D R Boggs, S S Boggs, D F Saxe, L A Gress, D R Canfield.   

Abstract

THIS STUDY WAS DESIGNED TO APPROACH TWO PRIMARY QUESTIONS CONCERNING HEMATOPOIETIC STEM CELLS (HSC) IN MICE: what is the concentration of HSC with extensive proliferative potential in marrow, and how long can an HSC continue to function in an intact animal? The assay system was the W/W(v) mouse, a mouse with an inherited HSC defect, reflected in a reduction in all myeloid tissue and most particularly in a macrocytic anemia.A single chromosomally marked HSC will reconstitute the defective hematopoietic system of the W/W(v). The concentration of HSC in normal littermate (+/+) marrow was assayed by limiting dilution calculation using cure of W/W(v) as an end point (correction of anemia and erythrocytes' macrocytosis) and found to be approximately 10/10(5). This is significantly less than spleen colony forming cell (CFU-S) concentration: approximately 220/10(5) in +/+ and ranging from 50 to 270/10(5) in various other studies. Blood values were studied at selected intervals for as long as 26 mo. Of 24 initially cured mice, which were observed for at least 2 yr, 75% remained cured. However, of all cured mice, 17 lost the cure, returning to a macrocytic anemic state. Cured mice had normal numbers of nucleated and granulocytic cells per humerus and a normal concentration of CFU-S. However, cure of secondary W/W(v) recipients by this marrow was inefficient compared with the original +/+ marrow. These studies suggest the CFU-S assay over-estimates extensively proliferating HSC or perhaps does not assay such a cell. A single such HSC can not only cure a W/W(v), but can sustain the cure for 2 yr or more, despite a relative deficit of cells capable of curing other W/W(v). However, the duration of sustained cure may be finite.

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Year:  1982        PMID: 6124553      PMCID: PMC371230          DOI: 10.1172/jci110611

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  52 in total

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2.  Observations on the settling and recoverability of transplanted hemopoietic colony-forming units in the mouse spleen.

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3.  Induced changes in transplantability of hemopoietic colony forming cells.

Authors:  S S Fred; W W Smith
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Authors:  D R Boggs; J C Marsh; P A Chervenick; G E Cartwright; M M Wintrobe
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5.  Antibody production by mice repopulated with limited numbers of clones of lymphoid cell precursors.

Authors:  J Trentin; N Wolf; V Cheng; W Fahlberg; D Weiss; R Bonhag
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6.  Decreased neutrophils and megakaryocytes in anemic mice of genotype W/W.

Authors:  P A Chervenick; D R Boggs
Journal:  J Cell Physiol       Date:  1969-02       Impact factor: 6.384

7.  The dilution factor of intravenously injected hemopoietic stem cells.

Authors:  G Matioli; H Vogel; H Niewisch
Journal:  J Cell Physiol       Date:  1968-12       Impact factor: 6.384

8.  Colony formation in agar by multipotential hemopoietic cells.

Authors:  D Metcalf; G R Johnson; T E Mandel
Journal:  J Cell Physiol       Date:  1979-02       Impact factor: 6.384

9.  Control of stem cell proliferation: a density-dependent committment model.

Authors:  J Prothero
Journal:  J Theor Biol       Date:  1980-06-21       Impact factor: 2.691

10.  Loss of proliferative capacity in immunohemopoietic stem cells caused by serial transplantation rather than aging.

Authors:  D E Harrison; C M Astle; J A Delaittre
Journal:  J Exp Med       Date:  1978-05-01       Impact factor: 14.307

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Authors:  S Hatada; K Nikkuni; S A Bentley; S Kirby; O Smithies
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3.  Spermatogonial stem cell enrichment by multiparameter selection of mouse testis cells.

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4.  In vitro proliferation of primitive hemopoietic stem cells supported by stromal cells: evidence for the presence of a mechanism(s) other than that involving c-kit receptor and its ligand.

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5.  Quantitative assay for totipotent reconstituting hematopoietic stem cells by a competitive repopulation strategy.

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6.  Clonal analysis of hematopoietic stem-cell differentiation in vivo.

Authors:  L G Smith; I L Weissman; S Heimfeld
Journal:  Proc Natl Acad Sci U S A       Date:  1991-04-01       Impact factor: 11.205

7.  Isolating gene-corrected stem cells without drug selection.

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8.  The role of CFU-GEMM in human hemopoiesis.

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Review 9.  Clones assemble! The clonal complexity of blood during ontogeny and disease.

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10.  Erythrocyte replacement precedes leukocyte replacement during repopulation of W/Wv mice with limiting dilutions of +/+ donor marrow cells.

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