Journals of Gerontology Series A: Biological Sciences and Medical Sciences Large Type Edition
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Li, Y.
Right arrow Articles by Wolf, N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Li, Y.
Right arrow Articles by Wolf, N.

Journals of Gerontology Series A: Biological Sciences and Medical Sciences, Vol 51, Issue 6 B403-B408, Copyright © 1996 by The Gerontological Society of America


JOURNAL ARTICLE

Cellular proliferative capacity and life span in small and large dogs

Y Li, B Deeb, W Pendergrass and N Wolf
Department of Pathology, University of Washington, Seattle, USA.

In a study comparing animal life spans and in vitro clonal proliferative capacity of skin fibroblasts in groupings of small, middle, large, and very large breeds of dogs of specific ages, the following results were obtained: (1) their life spans were inversely correlated to the frame sizes of the breeds; (2) the percent of large clones present in clone size distributions from the small dogs was inversely proportional to the age of the subjects (this was not true for the large breeds; however, animals older than 8 years were not available in those breeds); and (3) the group composed of the two largest breeds (Great Dane and Irish Wolfhound) had the shortest life spans and also had significantly smaller percentages of large skin fibroblast clones formed in vitro than either of the two groupings of smaller dogs at any age studied. It appears that within the domestic dogs the large body size is accompanied by shorter life span and, in the two largest breeds, decreased cellular growth potential.


This article has been cited by other articles:


Home page
J. Gerontol. A Biol. Sci. Med. Sci.Home page
R. N. Butler, S. N. Austad, N. Barzilai, A. Braun, S. Helfand, P. L. Larsen, A. M. McCormick, T. T. Perls, A. R. Shuldiner, R. L. Sprott, et al.
Longevity Genes: From Primitive Organisms to Humans
J. Gerontol. A Biol. Sci. Med. Sci., July 1, 2003; 58(7): B581 - 584.
[Full Text] [PDF]


Home page
Exp. Biol. Med.Home page
R. A. Miller, J. M. Harper, R. C. Dysko, S. J. Durkee, and S. N. Austad
Longer Life Spans and Delayed Maturation in Wild-Derived Mice
Experimental Biology and Medicine, July 1, 2002; 227(7): 500 - 508.
[Abstract] [Full Text] [PDF]


Home page
J. Gerontol. A Biol. Sci. Med. Sci.Home page
I. Dozmorov, A. Galecki, Y. Chang, R. Krzesicki, M. Vergara, and R. A. Miller
Gene Expression Profile of Long-Lived Snell Dwarf Mice
J. Gerontol. A Biol. Sci. Med. Sci., March 1, 2002; 57(3): B99 - 108.
[Abstract] [Full Text] [PDF]


Home page
J. Gerontol. A Biol. Sci. Med. Sci.Home page
I. Dozmorov, A. Bartke, and R. A. Miller
Array-Based Expression Analysis of Mouse Liver Genes: Effect of Age and of the Longevity Mutant Prop1df
J. Gerontol. A Biol. Sci. Med. Sci., February 1, 2001; 56(2): 72B - 80.
[Abstract] [Full Text]


Home page
J. Gerontol. A Biol. Sci. Med. Sci.Home page
R. A. Miller, C. Chrisp, and W. Atchley
Differential Longevity in Mouse Stocks Selected for Early Life Growth Trajectory
J. Gerontol. A Biol. Sci. Med. Sci., September 1, 2000; 55(9): 455B - 461.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
All GSA journals The Gerontologist
Journals of Gerontology Series B: Psychological Sciences and Social Sciences
Copyright © 1996 by The Gerontological Society of America.