The fraction of cells capable of division was determined for 1) population of the human diploid cell strains, W138 after different numbers of subcultivations in uitro and 2 ) a single population of W138 cells at intervals throughout its entire in vitro lifespan. In both cases the percentage of cells
A new cell surface marker of aging in human diploid fibroblasts
✍ Scribed by Shinichi Aizawa; Youji Mitsui
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 403 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The relationship of cell surface changes to proliferative decline of human diploid fibroblasts was investigated using the concanavalin A‐mediated red blood cell adsorption assay. The amount of the red blood cells adsorbed to human diploid fibroblasts via concanavalin A increased continously from the early phases of cell passage up through cell senescence, while the amount of ^3^H‐concanavalin A binding did not change to a significant extent. The red blood cell adsorption is not a function of cell cycle phase and time spent in culture. Cocultivation of young cells with old cells also did not affect the adsorption capacity of respective cells. Thus, the concanavalin A‐mediated red blood cell adsorption can be expected to serve as a new cell surface marker for aging in vitro. Using this marker, it was revealed that transient cell size or ^3^H‐thymidine incorporating capacity do not have a direct relationship with the division age of a cell. Small rapidly dividing cells in old populations resemble large slowly dividing or nondividing cells of the same populations and differ from small rapidly dividing cells in young populations, in terms of cell surface properties.
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