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Plasma protein and apolipoprotein synthesis by human yolk sac carcinoma cells in vitro
Authors:Robert E. Lanford  David L. Bronson  Larry E. Estlack  Frank H. Wians Jr.
Affiliation:(1) Present address: Department of Urologic Surgery, Room A-590, Box 394 Mayo, University of Minnesota Medical School, 420 Delaware St. S.E., 55455 Minneapolis, Minnesota;(2) Department of Virology and Immunology, Southwest Foundation for Biomedical Research, P.O. Box 28147, 78228 San Antonio, Texas;(3) Department of Pathology, Wilford Hall USAF Medical Center, Lackland AFB, 78236 San Antonio, Texas
Abstract:Summary Three human yolk sac carcinoma cell lines were characterized for the expression of several markers. Each of the cell lines expressed alpha-fetoprotein, without detectable levels of chorionic gonadotropin, and the level of alpha-fetoprotein expression increased dramatically when the cultures were held without passage for extended periods. The secretion of a number of plasma proteins was documented by metabolic labeling, immunoprecipitation, and gel analysis. The major plasma proteins detected were alpha-1-antitrypsin, alpha-fetoprotein, transthyretin,β-2 microglobulin, and plasminogen, with lower levels of transferrin and complement C4 released. Apolipoproteins B, E, and A1 were secreted in high levels as well and were found in the form of lipoprotein particles. Time course experiments on the synthesis of apolipoproteins E and A1 indicated that, as with alpha-fetoprotein, the level of synthesis increased substantially when the cultures were held without passage. The results indicate that these yolk sac carcinoma cells display a protein expression profile similar to that observed for the human yolk sac, and the possibility that the cells may have the potential to differentiate is discussed. This investigation was supported in part by Program Project HL 28972 from the National Heart, Lung and Blood Institute, Bethesda, MD.
Keywords:yolk sac carcinoma  plasma protein synthesis  lipoprotein synthesis
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