Tumor cells release intact portions of their plasma membranes in the process of membrane fragment shedding. This released material has been shown to inhibit various synthetic functions of normal cells, which may play an important role in certain patho-physiological events occurring in advanced-stage
Regulation of murine B lymphocyte plasma membrane protein turnover and shedding
β Scribed by Stephen G. Emerson; Robert E. Cone
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 960 KB
- Volume
- 109
- Category
- Article
- ISSN
- 0021-9541
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β¦ Synopsis
Abstract
Lactoperoxidaseβcatalyzed cell surface radioiodination was employed to radiolabel murine splenic Bβcell membrane immunoglobulins (IgM and IgD) and alloantigens encoded by the Major Histocompatibility Complex (IβA^k^, IβE^k^, Hβ2K^k^, Hβ2D^k^). The fate of the radiolabeled proteins was monitored by in vitro culture of labeled cells and isolation of labeled antigens from detergent lysates of the cells or culture fluids obtained at different times during culture. The effects of temperature, antimetabolites, colchicine, and cytochalasins on membrane protein catabolism demonstrated heterogeneity in rate, energy dependence, and cytoskeletal control of turnover suggesting that functional domains of turnover control exist in the B lymphocyte membrane.
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