The ultimate goal of this project is to determine whether cultured lymphocytes represent a superior model for studying in vitro senescence. Since the aging immune system has been postulated as one of the causes of biological aging, lymphocytes are an eminently suitable, yet heretofore unexplored, model for studying senescence in vitro. T cell cultures and clones will be established from normal newborn and adult lymphocytes, and will be analyzed for growth, functional and cell surface characteristics. Any clones which show unlimited growth, with no signs of senescence, will be examined for signs of transformation. Thus, the biological question of whether normal lymphocytes conform to the Hayflick limit will be addressed.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG005309-03
Application #
3115876
Study Section
Immunobiology Study Section (IMB)
Project Start
1985-09-30
Project End
1989-08-31
Budget Start
1987-09-01
Budget End
1989-08-31
Support Year
3
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
Schools of Medicine
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
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Effros, R B; Boucher, N; Porter, V et al. (1994) Decline in CD28+ T cells in centenarians and in long-term T cell cultures: a possible cause for both in vivo and in vitro immunosenescence. Exp Gerontol 29:601-9
Vaziri, H; Schachter, F; Uchida, I et al. (1993) Loss of telomeric DNA during aging of normal and trisomy 21 human lymphocytes. Am J Hum Genet 52:661-7
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Effros, R B; Walford, R L (1987) Neonatal T cells as a model system to study the possible in vitro senescence of lymphocytes. Exp Gerontol 22:307-16
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