Aggregation of chemically dissociated sponge cells in the absence of protein synthesis
โ Scribed by Humphreys, Tom
- Publisher
- John Wiley and Sons
- Year
- 1965
- Tongue
- English
- Weight
- 432 KB
- Volume
- 160
- Category
- Article
- ISSN
- 0022-104X
No coin nor oath required. For personal study only.
โฆ Synopsis
Puromycin and ethionine immediately inhibit protein synthesis more than 90% in chemically dissociated sponge cells. Initial aggregation proceeds normally in the presence of both inhibitors, indicating that protein synthesis is not necessary for the aggregation of these cells, After six hours in puromycin, the cells stop aggregating and die. In ethionine, the cells aggregate and remain aggregated for at least 48 hours, although protein synthesis remains repressed. Thus protein synthesis is not necessary for producing the material which binds these cells together. Although the aggregation is not dependent on concurrent protein synthesis, it was conceivable that protein which was stored in the cell was secreted during aggregation. However, sponge cells could aggregate over and over in ethionine, indicating that the cells were not dependent on a stored supply of material.
๐ SIMILAR VOLUMES
## Abstract V79โ8 cells lack a measurable G1 interval under normal growth conditions. We found that partial inhibition of protein synthesis using low levels of cycloheximide (0.05 ฮผ/ml) could induce a measurable G1 in these cells without any significant effects on S, G2, or M. In view of these find
A proteoglycan-like aggregation factor from the marine sponge Microciona prolqera (MAF) mediates cell-cell recognition via a cell-binding and a self-association domain. After repetitive and prolonged treatment of MAF with g1ycopeptide-Nglycosidase (PNGase) the specific binding of MAF to homotypic ce
## Activation of specific T cell lines by the antigens avidin and myelin basic protein in the absence of antigen-presenting cells We have investigated the specific activation by soluble antigen of rat or mouse longterm T helper cell lines using antigen-presenting cell (APC)-free culture conditions