Literature DB >> 788254

The fate of serially transplanted bone marrow cell populations from young and old donors.

D A Ogden, H S Mickliem.   

Abstract

Two bone marrow cell populations, separately identifiable by means of chromosome markers, were serially transferred at 8-10 week intervals through lethally irradiated syngeneic recipients. This system allowed a precise comparison of populations derived from young and old donors; no consistent differences were observed. Both donor populations ceased to replicate after 4-5 transfers. Although more than 10(3) spleen colony-forming units were transferred, the number of colones proliferating in the bone marrow fell sharply between the second and third transfer-generations. Regenerating host cells accounted for an increasing proportion of the miroses scord in the third and subsequent transfer generations. It is concluded that many of the stem cells of bone marrow subjected to two or more transfers have decreased powers of self renewal. The results suggest that stem cells of adult mouse bone marrow are capable of undergoing, at most, between 80 and 200 mitoses. This limitation is very possibly innate, but the possibility that it is an artifact of the serial transfer system cannot be entirely ruled out.

Entities:  

Mesh:

Year:  1976        PMID: 788254     DOI: 10.1097/00007890-197609000-00010

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  30 in total

Review 1.  When stem cells grow old: phenotypes and mechanisms of stem cell aging.

Authors:  Michael B Schultz; David A Sinclair
Journal:  Development       Date:  2016-01-01       Impact factor: 6.868

2.  Cell intrinsic alterations underlie hematopoietic stem cell aging.

Authors:  Derrick J Rossi; David Bryder; Jacob M Zahn; Henrik Ahlenius; Rebecca Sonu; Amy J Wagers; Irving L Weissman
Journal:  Proc Natl Acad Sci U S A       Date:  2005-06-20       Impact factor: 11.205

3.  Age-related defects in B lymphopoiesis underlie the myeloid dominance of adult leukemia.

Authors:  Robert A J Signer; Encarnacion Montecino-Rodriguez; Owen N Witte; Jami McLaughlin; Kenneth Dorshkind
Journal:  Blood       Date:  2007-06-06       Impact factor: 22.113

4.  AKT1 and AKT2 maintain hematopoietic stem cell function by regulating reactive oxygen species.

Authors:  Marisa M Juntilla; Vineet D Patil; Marco Calamito; Rohan P Joshi; Morris J Birnbaum; Gary A Koretzky
Journal:  Blood       Date:  2010-03-30       Impact factor: 22.113

Review 5.  Aging stem cells, latexin, and longevity.

Authors:  Ying Liang; Gary Van Zant
Journal:  Exp Cell Res       Date:  2008-02-19       Impact factor: 3.905

6.  Cytogerontology since 1881: a reappraisal of August Weismann and a review of modern progress.

Authors:  T B Kirkwood; T Cremer
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

7.  Effects of aging on the homing and engraftment of murine hematopoietic stem and progenitor cells.

Authors:  Ying Liang; Gary Van Zant; Stephen J Szilvassy
Journal:  Blood       Date:  2005-04-12       Impact factor: 22.113

8.  Effects of aging and niche microenvironment on spermatogonial stem cell self-renewal.

Authors:  Buom-Yong Ryu; Kyle E Orwig; Jon M Oatley; Mary R Avarbock; Ralph L Brinster
Journal:  Stem Cells       Date:  2006-02-02       Impact factor: 6.277

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

Authors:  D R Boggs; S S Boggs; D F Saxe; L A Gress; D R Canfield
Journal:  J Clin Invest       Date:  1982-08       Impact factor: 14.808

10.  Modeling of replicative senescence in hematopoietic development.

Authors:  Anna Marciniak-Czochra; Thomas Stiehl; Wolfgang Wagner
Journal:  Aging (Albany NY)       Date:  2009-07-23       Impact factor: 5.682

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.