Literature DB >> 6129277

Loss of stem cell repopulating ability upon transplantation. Effects of donor age, cell number, and transplantation procedure.

D E Harrison, C M Astle.   

Abstract

Long-term functional capacities of marrow cell lines were defined by competitive repopulation, a technique capable of detecting a small decline in repopulating abilities. There was little or no difference between cells from old and young donors, but a single serial transplantation caused a large decline in repopulating ability. Varying the numbers of marrow cells transplanted into the initial carrier from 10(5) to 10(7) did not alter the ability of the carrier's marrow cells to repopulate in competition with previously untransplanted cells. This ability was improved only in carriers that had received 10(8) marrow cells, although deleterious effects of transplantation were still present. These effects were not solely caused by cell damage from the transplantation procedure, because transplantation by parabiosis, or recovery from sublethal irradiation without transplantation, reduced repopulating abilities as much as transplanting 10(5) to 10(7) marrow cells. The transplantation effect also was not caused solely by irradiation, because the same effect appeared in unirradiated W/Wv carriers. The transplantation effect was more pronounced when donors were identified by hemoglobin type than by chromosome markers, implying that nonerythroid cell lines may be less affected by transplantation than erythroid precursor cells. When the effects of a lifetime of normal function and a single transplantation were compared, the latter caused 3-7 times more decline in repopulating abilities of phytohemagglutinin-responsive cell precursors, and at least 10-20 times more decline in erythroid cell precursors. Stem cell lines can be serially transplanted at least five times before losing their ability to repopulate and save lethally irradiated recipients or to cure genetically anemic mice. Therefore, if transplantation causes an acceleration of the normal aging process, these figures suggest that stem cells should be able to function normally through at least 15-50 life spans.

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Mesh:

Year:  1982        PMID: 6129277      PMCID: PMC2186863          DOI: 10.1084/jem.156.6.1767

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  35 in total

1.  LYMPHOCYTE CONTENT AND PROLIFERATIVE CAPACITY OF SERIALLY TRANSPLANTED MOUSE BONE MARROW.

Authors:  G CUDKOWICZ; A C UPTON; G M SHEARER; W L HUGHES
Journal:  Nature       Date:  1964-01-11       Impact factor: 49.962

2.  [Serial grafts of homologous bone marrow in irradiated mice].

Authors:  D W BARNES; C E FORD; J F LOUTIT
Journal:  Sang       Date:  1959

Review 3.  Proliferative capacity of erythropoietic stem cell lines and aging: an overview.

Authors:  D E Harrison
Journal:  Mech Ageing Dev       Date:  1979-03       Impact factor: 5.432

4.  Jerne plaque assay for antibody-forming spleen cells: some technical modifications.

Authors:  N Kaliss
Journal:  Transplantation       Date:  1971-08       Impact factor: 4.939

5.  Immunologic deficiencies in senescence. II. Characterization of extrinsic deficiencies.

Authors:  G B Price; T Makinodan
Journal:  J Immunol       Date:  1972-02       Impact factor: 5.422

6.  Nature of the hemopoietic stem cell compartment and its proliferative potential.

Authors:  L E Botnick; E C Hannon; S Hellman
Journal:  Blood Cells       Date:  1979-06-15

Review 7.  Parabiosis in immunobiology.

Authors:  N W Nisbet
Journal:  Transplant Rev       Date:  1973

8.  The relationship between the spleen colony-forming cell and the haemopoietic stem cell.

Authors:  R Schofield
Journal:  Blood Cells       Date:  1978

9.  Allogeneic bone marrow transplantation for chronic granulocytic leukemia.

Authors:  K C Doney; C D Buckner; E D Thomas; J Sanders; R A Clift; J A Hansen; G E Sale; J Singer; R Storb
Journal:  Exp Hematol       Date:  1981-11       Impact factor: 3.084

10.  A comparison of marrow transplantation with chemotherapy for children with acute lymphoblastic leukemia in second or subsequent remission.

Authors:  F L Johnson; E D Thomas; B S Clark; R L Chard; J R Hartmann; R Storb
Journal:  N Engl J Med       Date:  1981-10-08       Impact factor: 91.245

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  82 in total

1.  The repopulation potential of hepatocyte populations differing in size and prior mitotic expansion.

Authors:  K Overturf; M Al-Dhalimy; M Finegold; M Grompe
Journal:  Am J Pathol       Date:  1999-12       Impact factor: 4.307

2.  Functionally distinct hematopoietic stem cells modulate hematopoietic lineage potential during aging by a mechanism of clonal expansion.

Authors:  Isabel Beerman; Deepta Bhattacharya; Sasan Zandi; Mikael Sigvardsson; Irving L Weissman; David Bryder; Derrick J Rossi
Journal:  Proc Natl Acad Sci U S A       Date:  2010-03-18       Impact factor: 11.205

3.  RNAi screen for telomerase reverse transcriptase transcriptional regulators identifies HIF1alpha as critical for telomerase function in murine embryonic stem cells.

Authors:  Matthew Coussens; Philip Davy; Lancer Brown; Christopher Foster; William H Andrews; Melissa Nagata; Richard Allsopp
Journal:  Proc Natl Acad Sci U S A       Date:  2010-07-19       Impact factor: 11.205

4.  Identification of a new intrinsically timed developmental checkpoint that reprograms key hematopoietic stem cell properties.

Authors:  Michelle B Bowie; David G Kent; Brad Dykstra; Kristen D McKnight; Lindsay McCaffrey; Pamela A Hoodless; Connie J Eaves
Journal:  Proc Natl Acad Sci U S A       Date:  2007-03-22       Impact factor: 11.205

5.  The GOD of hematopoietic stem cells: a clonal diversity model of the stem cell compartment.

Authors:  C E Muller-Sieburg; H B Sieburg
Journal:  Cell Cycle       Date:  2006-02-15       Impact factor: 4.534

6.  The Polycomb group gene Ezh2 prevents hematopoietic stem cell exhaustion.

Authors:  Leonie M Kamminga; Leonid V Bystrykh; Aletta de Boer; Sita Houwer; José Douma; Ellen Weersing; Bert Dontje; Gerald de Haan
Journal:  Blood       Date:  2005-11-17       Impact factor: 22.113

7.  Deletion of Puma protects hematopoietic stem cells and confers long-term survival in response to high-dose gamma-irradiation.

Authors:  Hui Yu; Hongmei Shen; Youzhong Yuan; Richard XuFeng; Xiaoxia Hu; Sean P Garrison; Lin Zhang; Jian Yu; Gerard P Zambetti; Tao Cheng
Journal:  Blood       Date:  2010-02-22       Impact factor: 22.113

8.  Nfatc1 orchestrates aging in hair follicle stem cells.

Authors:  Brice E Keyes; Jeremy P Segal; Evan Heller; Wen-Hui Lien; Chiung-Ying Chang; Xingyi Guo; Dan S Oristian; Deyou Zheng; Elaine Fuchs
Journal:  Proc Natl Acad Sci U S A       Date:  2013-11-26       Impact factor: 11.205

9.  Thrombopoietic potential and serial repopulating ability of murine hematopoietic stem cells constitutively expressing interleukin 11.

Authors:  R G Hawley; T S Hawley; A Z Fong; C Quinto; M Collins; J P Leonard; S J Goldman
Journal:  Proc Natl Acad Sci U S A       Date:  1996-09-17       Impact factor: 11.205

10.  Unrelated donors are associated with improved relapse-free survival compared to related donors in patients with myelodysplastic syndrome undergoing reduced intensity allogeneic stem cell transplantation.

Authors:  Clinton Yam; Lisa Crisalli; Selina M Luger; Alison W Loren; Elizabeth O Hexner; Noelle V Frey; James K Mangan; Amy Gao; Edward A Stadtmauer; David L Porter; Ran Reshef
Journal:  Am J Hematol       Date:  2016-07-12       Impact factor: 10.047

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