Literature DB >> 1091693

Normal function of transplanted marrow cell lines from aged mice.

D E Harrison.   

Abstract

Transplantation experiments indicated that losses with age in erythrocyte production were not intrinsically timed within marrow cell lines. In most cases marrow cell lines from old donors functioned as well as those from young donors after transplantation into either W/W-v anemic or lethally irradiated normal recipients. After normal marrow cells had been serially transplanted into successive W/W-v mice 5 times, both old and young cell lines began to fail; the old cell lines had produced erythrocytes normally for 77 to 84 mo. Transplanted old and young control marrow cell lines, identified by T6 chromosomes, saved the lives of lethally irradiated recipients; the oldest cell lines functioned normally for 54 mo. The hypothesis is suggested that senescence of an organism is caused by intrinsically timed functional declines in only a few vital cell types. In transplantation experiments to identify these cell types, four criteria--function, identification, control, and health--should be met. The marrow transplantation experiments led to and illustrate the hypothesis and the four criteria.

Entities:  

Mesh:

Year:  1975        PMID: 1091693     DOI: 10.1093/geronj/30.3.279

Source DB:  PubMed          Journal:  J Gerontol        ISSN: 0022-1422


  10 in total

Review 1.  Senescence of hematopoietic stem cells and bone marrow failure.

Authors:  Jichun Chen
Journal:  Int J Hematol       Date:  2005-10       Impact factor: 2.490

2.  Proliferative capacity of murine hematopoietic stem cells.

Authors:  S Hellman; L E Botnick; E C Hannon; R M Vigneulle
Journal:  Proc Natl Acad Sci U S A       Date:  1978-01       Impact factor: 11.205

Review 3.  Cellular aging--clonal senescence. A review (Part I).

Authors:  G M Martin
Journal:  Am J Pathol       Date:  1977-11       Impact factor: 4.307

Review 4.  Hematopoietic stem cell development, aging and functional failure.

Authors:  Jichun Chen
Journal:  Int J Hematol       Date:  2011-04-27       Impact factor: 2.490

5.  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

6.  Relationship between donor age and the replicative lifespan of human cells in culture: a reevaluation.

Authors:  V J Cristofalo; R G Allen; R J Pignolo; B G Martin; J C Beck
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-01       Impact factor: 11.205

7.  F1 hybrid resistance: long-term systemic effects sensitive to irradiation and age.

Authors:  D E Harrison
Journal:  Immunogenetics       Date:  1981       Impact factor: 2.846

8.  Comparative endocrinology of aging and longevity regulation.

Authors:  John B Allard; Cunming Duan
Journal:  Front Endocrinol (Lausanne)       Date:  2011-11-23       Impact factor: 5.555

9.  Decline in the growth potential of spleen-colonizing bone marrow stem cells of long-lived aging mice.

Authors:  J W Albright; T Makinodan
Journal:  J Exp Med       Date:  1976-11-02       Impact factor: 14.307

10.  Serial depletion and regeneration of the murine hematopoietic system. Implications for hematopoietic organization and the study of cellular aging.

Authors:  E A Ross; N Anderson; H S Micklem
Journal:  J Exp Med       Date:  1982-02-01       Impact factor: 14.307

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.