Literature DB >> 7892220

Behavior of hematopoietic stem cells in a large animal.

J L Abkowitz1, M T Persik, G H Shelton, R L Ott, J V Kiklevich, S N Catlin, P Guttorp.   

Abstract

To study the behavior of hematopoietic stem cells in vivo, we transplanted glucose-6-phosphate dehydrogenase (G6PD) heterozygous (female Safari) cats with small amounts of autologous marrow. The G6PD phenotypes of erythroid burst-forming units and granulocyte/macrophage colony-forming units were repeatedly assayed for 3.5-6 years after transplantation to track contributions of stem cell clones to the progenitor cell compartment. Two phases of stem cell kinetics were observed, which were similar to the pattern reported in comparable murine studies. Initially there were significant fluctuations in contributions of stem cell clones. Later clonal contributions to hematopoiesis stabilized. The initial phase of clonal disequilibrium, however, extended for 1-4.5 years (and not 2-6 months as seen in murine experiments). After this subsided, all progenitor cells from some animals expressed a single parental G6PD phenotype, suggesting that blood cell production could be stably maintained by the progeny of one (or a few) cells. As the hematopoietic demand of a cat (i.e., number of blood cells produced per lifetime) is over 600 times that of a mouse, this provides evidence that an individual hematopoietic stem cell has a vast self-renewal and/or proliferative capacity. The long phase of clonal instability may reflect the time required for stem cells to replicate sufficiently to reconstitute a large stem cell reserve.

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Year:  1995        PMID: 7892220      PMCID: PMC42417          DOI: 10.1073/pnas.92.6.2031

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  21 in total

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Authors:  S Nakao; M Yamaguchi; H Takamatsu; S Shiobara; T Matsuda
Journal:  Transplantation       Date:  1994-04-27       Impact factor: 4.939

5.  Clonal hematopoiesis demonstrated by X-linked DNA polymorphisms after allogeneic bone marrow transplantation.

Authors:  A G Turhan; R K Humphries; G L Phillips; A C Eaves; C J Eaves
Journal:  N Engl J Med       Date:  1989-06-22       Impact factor: 91.245

6.  A prospective study of the value of bone marrow erythroid progenitor cultures in polycythemia.

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7.  Nonclonal hemopoietic progenitors in a G6PD heterozygote with chronic myelogenous leukemia revealed after long-term marrow culture.

Authors:  D E Hogge; L Coulombel; D K Kalousek; C J Eaves; A C Eaves
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8.  Use of an X-linked human neutrophil marker to estimate timing of lyonization and size of the dividing stem cell pool.

Authors:  E S Buescher; D W Alling; J I Gallin
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9.  Large numbers of primitive stem cells are active simultaneously in aggregated embryo chimeric mice.

Authors:  D E Harrison; C Lerner; P C Hoppe; G A Carlson; D Alling
Journal:  Blood       Date:  1987-03       Impact factor: 22.113

10.  Number and continuous proliferative pattern of transplanted primitive immunohematopoietic stem cells.

Authors:  D E Harrison; C M Astle; C Lerner
Journal:  Proc Natl Acad Sci U S A       Date:  1988-02       Impact factor: 11.205

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  28 in total

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4.  On the probability of random genetic mutations for various types of tumor growth.

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Authors:  David Dingli; Arne Traulsen; Jorge M Pacheco
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Review 8.  Hematopoietic stem cell gene therapy:assessing the relevance of preclinical models.

Authors:  Andre Larochelle; Cynthia E Dunbar
Journal:  Semin Hematol       Date:  2013-04       Impact factor: 3.851

Review 9.  The potential of non-myeloablative heterochronous autologous hematopoietic stem cell transplantation for extending a healthy life span.

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Journal:  Geroscience       Date:  2018-06-14       Impact factor: 7.713

10.  Mathematical modeling of therapeutic strategies for myeloid malignancies.

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