Some Structural and Antigenic Properties of Intracisternal A Particles Occurring in Mouse Tumors

Intracisternal A-particles were isolated from three different myeloma lines in BALB/c mice and from cultured neuroblastoma cells of A/J origin. All preparations contained a major structural protein with an apparent molecular weight near 70,000 as estimated by electrophoretic mobility in sodium dodec...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 69; no. 1; pp. 218 - 222
Main Authors Kuff, Edward L., Lueders, Kira K., Ozer, Harvey L., Wivel, Nelson A.
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences of the United States of America 01.01.1972
National Acad Sciences
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Abstract Intracisternal A-particles were isolated from three different myeloma lines in BALB/c mice and from cultured neuroblastoma cells of A/J origin. All preparations contained a major structural protein with an apparent molecular weight near 70,000 as estimated by electrophoretic mobility in sodium dodecyl sulfate-containing polyacrylamide gels. Solubilization of this component by sodium dodecyl sulfate was dependent on prior or concomitant treatment with sulfhydryl compounds. The size distribution of A-particle proteins was markedly different from that observed for extracellular murine leukemia and mammary tumor viruses. Rabbit antiserum was developed that reacted with the major A-particle protein in both complement fixation and immunodiffusion assays. The antigen was detected in isolated neuroblastoma A-particles, in cytoplasmic membrane fractions prepared from various mouse tumors known to contain intracisternal particles, but not in preparations from normal mouse cells, in samples of leukemia and mammary tumor virus, or in JLS-V9 cells infected with Rauscher leukemia virus. Conversely, isolated A-particles did not react in complement fixation or immunodiffusion assays with antisera against leukemia virus antigens.
AbstractList Intracisternal A-particles were isolated from three different myeloma lines in BALB/c mice and from cultured neuroblastoma cells of A/J origin. All preparations contained a major structural protein with an apparent molecular weight near 70,000 as estimated by electrophoretic mobility in sodium dodecyl sulfate-containing polyacrylamide gels. Solubilization of this component by sodium dodecyl sulfate was dependent on prior or concomitant treatment with sulfhydryl compounds. The size distribution of A-particle proteins was markedly different from that observed for extracellular murine leukemia and mammary tumor viruses. Rabbit antiserum was developed that reacted with the major A-particle protein in both complement fixation and immunodiffusion assays. The antigen was detected in isolated neuroblastoma A-particles, in cytoplasmic membrane fractions prepared from various mouse tumors known to contain intracisternal particles, but not in preparations from normal mouse cells, in samples of leukemia and mammary tumor virus, or in JLS-V9 cells infected with Rauscher leukemia virus. Conversely, isolated A-particles did not react in complement fixation or immunodiffusion assays with antisera against leukemia virus antigens.
Intracisternal A-particles were isolated from three different myeloma lines in BALB/c mice and from cultured neuroblastoma cells of A/J origin. All preparations contained a major structural protein with an apparent molecular weight near 70,000 as estimated by electrophoretic mobility in sodium dodecyl sulfate-containing polyacrylamide gels. Solubilization of this component by sodium dodecyl sulfate was dependent on prior or concomitant treatment with sulfhydryl compounds. The size distribution of A-particle proteins was markedly different from that observed for extracellular murine leukemia and mammary tumor viruses. Rabbit antiserum was developed that reacted with the major A-particle protein in both complement fixation and immunodiffusion assays. The antigen was detected in isolated neuroblastoma A-particles, in cytoplasmic membrane fractions prepared from various mouse tumors known to contain intracisternal particles, but not in preparations from normal mouse cells, in samples of leukemia and mammary tumor virus, or in JLS-V9 cells infected with Rauscher leukemia virus. Conversely, isolated A-particles did not react in complement fixation or immunodiffusion assays with antisera against leukemia virus antigens. complement fixation immunodiffusion neuroblastoma plasma-cell tumor
Author Lueders, Kira K.
Wivel, Nelson A.
Ozer, Harvey L.
Kuff, Edward L.
AuthorAffiliation Laboratory of Biochemistry, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20014
Laboratory of Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20014
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Snippet Intracisternal A-particles were isolated from three different myeloma lines in BALB/c mice and from cultured neuroblastoma cells of A/J origin. All...
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SubjectTerms Animals
Antigens
Antiserum
Biological Sciences: Biochemistry
Bone Marrow - immunology
Carcinoma, Ehrlich Tumor - immunology
Cell Line
Cell Membrane - immunology
Complement Fixation Tests
Fibroblasts - immunology
Gels
Immune Sera
Immunodiffusion
Immunoelectrophoresis
Kidney - immunology
Leukemia L1210 - immunology
Liver - immunology
Mammary Tumor Virus, Mouse - immunology
Mice
Mice, Inbred Strains
Moloney murine leukemia virus - immunology
Multiple Myeloma - immunology
Neoplasms, Experimental - immunology
Neuroblastoma
Neuroblastoma - immunology
Neurons
Oncogenic viruses
Rauscher Virus - immunology
Sodium
Spleen - immunology
Subcellular Fractions - immunology
Tumors
Viruses
Title Some Structural and Antigenic Properties of Intracisternal A Particles Occurring in Mouse Tumors
URI https://www.jstor.org/stable/61016
http://www.pnas.org/content/69/1/218.abstract
https://www.ncbi.nlm.nih.gov/pubmed/4333040
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Volume 69
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