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 Park, S. C.
Right arrow Articles by Kwak, S. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Park, S. C.
Right arrow Articles by Kwak, S. J.

Journals of Gerontology Series A: Biological Sciences and Medical Sciences, Vol 54, Issue 2 B78-B83, Copyright © 1999 by The Gerontological Society of America


JOURNAL ARTICLE

Aging process is accompanied by increase of transglutaminase C

SC Park, EJ Yeo, JA Han, YC Hwang, JY Choi, JS Park, YH Park, KO Kim, IG Kim, SC Seong and SJ Kwak
Department of Biochemistry, Seoul National University College of Medicine, Republic of Korea. scpark@plaza.snu.ac.kr

Crosslinking has been suggested as one of the mechanisms involved in the aging process. Among the various random or enzyme-mediated crosslinking reactions, transglutaminase (TGase)-catalyzed crosslinking activity has been proposed for its possible involvement in cell proliferation, differentiation, carcinogenesis, programmed death, and aging. Moreover, recent findings of TGase C as a putative signal transducer and cell cycle regulator has renewed interest in the study of TGase C in relation to aging phenomena. The ubiquitous presence of TGase C compared to the organ-specific localization of other types of TGases has attracted special attention as a cellular aging device. In the present investigation for in vitro studies, we have compared the pattern of TGase C in young and old human red blood cells, separated by density differentiation, and in early and late-passage or hydrogen peroxide-treated human primary fibroblasts. For in vivo study, we monitored the age-dependent changes of TGase C in the liver and brain tissues of 4, 12, 18, and 24-month-old Sprague-Dawley rats. We obtained evidence that both the activity and protein levels of TGase C were high in old RBC and late-passage or hydrogen peroxide-treated fibroblasts. Similar findings were seen in liver and brain tissue such as age- dependent increases in TGase activity and protein level in an organ- specific pattern. These data suggest that TGase C might play an active role in the cellular process with age.


This article has been cited by other articles:


Home page
IOVSHome page
J. R. Dunlevy and J. A. S. Rada
Interaction of Lumican with Aggrecan in the Aging Human Sclera
Invest. Ophthalmol. Vis. Sci., November 1, 2004; 45(11): 3849 - 3856.
[Abstract] [Full Text] [PDF]




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 © 1999 by The Gerontological Society of America.