| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
American Journal of Pathology, Vol 151, 659-663, Copyright © 1997 by American Society for Investigative Pathology
REGULAR ARTICLES |
Y Higami, I Shimokawa, M Tomita, T Okimoto, T Koji, N Kobayashi and T Ikeda
Department of Pathology, Nagasaki University School of Medicine, Japan.
Aging enhances apoptosis of hepatocytes under normal physiological conditions and increases the susceptibility of hepatocytes to apoptosis whereas life-long dietary restriction suppresses the age-enhanced susceptibility to apoptosis. We examined the subcellular mechanisms of the age-associated changes and effect of dietary restriction using quantitative reverse transcription polymerase chain reaction and immunohistochemistry for Fas in the livers of 6- and 24-month-old male Fischer 344 rats fed ad libitum or 70% diet restricted. We also analyzed the level of ordinary and variant forms of Fas mRNA. The ordinary form of Fas mRNA, but not the variant form of Fas mRNA, significantly increased with age. Dietary restriction significantly suppressed the ordinary form of Fas mRNA in advanced age. Aging enhanced Fas immunoreactivity in the hyperplastic bile epithelium and hepatocytes whereas dietary restriction suppressed it. Our findings indicate that Fas protein, particularly the ordinary form of Fas, is involved in age-associated apoptosis of hepatocytes. Fas overexpression in advanced age may explain the age-enhanced susceptibility to apoptosis. Our results also suggest that dietary restriction suppresses Fas overexpression, resulting in a reduction of the age-enhanced susceptibility to apoptosis.
This article has been cited by other articles:
![]() |
V. Molpeceres, J. L. Mauriz, M. V. Garcia-Mediavilla, P. Gonzalez, J. P. Barrio, and J. Gonzalez-Gallego Melatonin Is Able to Reduce the Apoptotic Liver Changes Induced by Aging Via Inhibition of the Intrinsic Pathway of Apoptosis J. Gerontol. A Biol. Sci. Med. Sci., July 1, 2007; 62(7): 687 - 695. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Higami, T. Tsuchiya, T. Chiba, H. Yamaza, I. Muraoka, M. Hirose, T. Komatsu, and I. Shimokawa Hepatic Gene Expression Profile of Lipid Metabolism in Rats: Impact of Caloric Restriction and Growth Hormone/Insulin-Like Growth Factor-1 Suppression J. Gerontol. A Biol. Sci. Med. Sci., November 1, 2006; 61(11): 1099 - 1110. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Qiao, X. Chen, D. Wu, R. Ding, J. Wang, Q. Hong, S. Shi, J. Li, Y. Xie, Y. Lu, et al. Mitochondrial Pathway Is Responsible for Aging-Related Increase of Tubular Cell Apoptosis in Renal Ischemia/Reperfusion Injury J. Gerontol. A Biol. Sci. Med. Sci., June 1, 2005; 60(7): 830 - 839. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Pinti, L. Troiano, M. Nasi, C. Bellodi, R. Ferraresi, C. Mussi, G. Salvioli, and A. Cossarizza Balanced Regulation of mRNA Production for Fas and Fas Ligand in Lymphocytes From Centenarians: How the Immune System Starts Its Second Century Circulation, November 9, 2004; 110(19): 3108 - 3114. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Chigira, K. Sugita, K. Kita, S. Sugaya, Y. Arase, M. Ichinose, H. Shirasawa, and N. Suzuki Increased Expression of the Huntingtin Interacting Protein-1 Gene in Cells From Hutchinson Gilford Syndrome (Progeria) Patients and Aged Donors J. Gerontol. A Biol. Sci. Med. Sci., October 1, 2003; 58(10): B873 - 878. [Abstract] [Full Text] [PDF] |
||||
![]() |
Q. J. Li, M. F. Ashraf, D. Shen, W. R. Green, W. J. Stark, C.-C. Chan, and T. P. O'Brien The Role of Apoptosis in the Pathogenesis of Fuchs Endothelial Dystrophy of the Cornea Arch Ophthalmol, November 1, 2001; 119(11): 1597 - 1604. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. D. Pugh, T. D. Oberley, and R. Weindruch Dietary Intervention at Middle Age: Caloric Restriction but not Dehydroepiandrosterone Sulfate Increases Lifespan and Lifetime Cancer Incidence in Mice Cancer Res., April 1, 1999; 59(7): 1642 - 1648. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |