|
|
||||||||
1Cellular and Molecular Biology Graduate Program, University of Michigan School of Medicine, Ann Arbor, Michigan; 2Department of Biochemistry and Molecular Biology, University of Louisville, Louisville, Kentucky; 3Departments of Internal Medicine and Physiology, Geriatrics Research, Southern Illinois University, School of Medicine, Springfield, Illinois; 4Edison Biotechnology Institute and Department of Biomedical Sciences, Ohio University, Athens, Ohio; 5Department of Pathology, University of Michigan School of Medicine; and 6University of Michigan Geriatrics Center and Institute of Gerontology and the Ann Arbor Department of Veterans Affairs Medical Center, Ann Arbor Michigan
Submitted 7 December 2004 ; accepted in final form 2 February 2005
Previous studies have shown that dermal fibroblast cell lines derived from young adult mice of the long-lived Snell dwarf mutant stock are resistant, in vitro, to the cytotoxic effects of H2O2, cadmium, UV light, paraquat, and heat. We show here that similar resistance profiles are seen in fibroblast cells derived from a related mutant, the Ames dwarf mouse, and that cells from growth hormone receptor-null mice are resistant to H2O2, paraquat, and UV but not to cadmium. Resistance to UV light, cadmium, and H2O2 are similar in cells derived from 1-wk-old Snell dwarf or normal mice, and thus the resistance of cell lines derived from young adult donors reflects developmental processes, presumably hormone dependent, that take place in the first few months of life. The resistance of cells from Snell dwarf mice to these stresses does not reflect merely antioxidant defenses: dwarf-derived cells are also resistant to the DNA-alkylating agent methyl methanesulfonate. Furthermore, inhibitor studies show that fibroblast resistance to UV light is unaffected by the antioxidants ascorbic acid and N-acetyl-L-cysteine. These data suggest that postnatal exposure to altered levels of pituitary hormones leads to development of cellular resistance to oxidative and nonoxidative stressors, which are stable through many rounds of in vitro cell division and could contribute to the remarkable disease resistance of long-lived mutant mice.
oxidation; life span; Snell dwarf; aging; insulin-like growth factor I
This article has been cited by other articles:
![]() |
A. B. Salmon, M. Ljungman, and R. A. Miller Cells From Long-Lived Mutant Mice Exhibit Enhanced Repair of Ultraviolet Lesions J. Gerontol. A Biol. Sci. Med. Sci., March 1, 2008; 63(3): 219 - 231. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. B. Salmon, A. A. S. Akha, R. Buffenstein, and R. A. Miller Fibroblasts From Naked Mole-Rats Are Resistant to Multiple Forms of Cell Injury, But Sensitive to Peroxide, Ultraviolet Light, and Endoplasmic Reticulum Stress J. Gerontol. A Biol. Sci. Med. Sci., March 1, 2008; 63(3): 232 - 241. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. M. Smith, J. T. Hoi, J. C. Eissenberg, J. D. Shoemaker, W. S. Neckameyer, A. M. Ilvarsonn, L. G. Harshman, V. L. Schlegel, and J. Zempleni Feeding Drosophila a Biotin-Deficient Diet for Multiple Generations Increases Stress Resistance and Lifespan and Alters Gene Expression and Histone Biotinylation Patterns J. Nutr., September 1, 2007; 137(9): 2006 - 2012. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Csiszar, N. Labinskyy, Z. Orosz, Z. Xiangmin, R. Buffenstein, and Z. Ungvari Vascular aging in the longest-living rodent, the naked mole rat Am J Physiol Heart Circ Physiol, August 1, 2007; 293(2): H919 - H927. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Ungvari, Z. Orosz, A. Rivera, N. Labinskyy, Z. Xiangmin, S. Olson, A. Podlutsky, and A. Csiszar Resveratrol increases vascular oxidative stress resistance Am J Physiol Heart Circ Physiol, May 1, 2007; 292(5): H2417 - H2424. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Labinskyy, A. Csiszar, Z. Orosz, K. Smith, A. Rivera, R. Buffenstein, and Z. Ungvari Comparison of endothelial function, O2-{middle dot} and H2O2 production, and vascular oxidative stress resistance between the longest-living rodent, the naked mole rat, and mice. Am J Physiol Heart Circ Physiol, December 1, 2006; 291(6): H2698 - H2704. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. C. Corton and H. M. Brown-Borg Peroxisome Proliferator-Activated Receptor {gamma} Coactivator 1 in Caloric Restriction and Other Models of Longevity J. Gerontol. A Biol. Sci. Med. Sci., December 1, 2005; 60(12): 1494 - 1509. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |