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Studies of Neoplastic Myelomonocytic Cells in BALB/c Mice Producing Infectious C-Type Viruses

Studies of Neoplastic Myelomonocytic Cells in BALB/c Mice Producing Infectious C-Type Viruses C-type viruses were identified by electron microscopy in muramidase-producing transplantable leukemic cells of BALB/c mice. Neoplastic cells contained peroxidase-positive cytoplasmic granules and consisted of atypical monocytic and granulocytic precursors, undifferentiated stem cells, and histiocytes. Viral particles were present in all tumors studied and were principally of the intracisternal A and immature C types. Exceptionally, mature C-type virions were noted in large cytoplasmic vacuoles of tumor cells, in bone marrow megakaryocytes, and in extracellular spaces. Unusual cytoplasmic structures that may represent structural precursors of viral nucleoprotein assembly were also observed in some cells. Bone marrow cells from animals treated with cell-free filtrates contained numerous cylindrical inclusions, several of which demonstrated viral budding. Complement fixation and mouse embryo cytopathogenicity tests on tumor extracts identified the viral particles as members of the murine leukemia-sarcoma group and demonstrated high titers of infectivity. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Cancer Research American Association of Cancer Research

Studies of Neoplastic Myelomonocytic Cells in BALB/c Mice Producing Infectious C-Type Viruses

Cancer Research , Volume 33 (4): 671 – Apr 1, 1973

Studies of Neoplastic Myelomonocytic Cells in BALB/c Mice Producing Infectious C-Type Viruses

Cancer Research , Volume 33 (4): 671 – Apr 1, 1973

Abstract

C-type viruses were identified by electron microscopy in muramidase-producing transplantable leukemic cells of BALB/c mice. Neoplastic cells contained peroxidase-positive cytoplasmic granules and consisted of atypical monocytic and granulocytic precursors, undifferentiated stem cells, and histiocytes. Viral particles were present in all tumors studied and were principally of the intracisternal A and immature C types. Exceptionally, mature C-type virions were noted in large cytoplasmic vacuoles of tumor cells, in bone marrow megakaryocytes, and in extracellular spaces. Unusual cytoplasmic structures that may represent structural precursors of viral nucleoprotein assembly were also observed in some cells. Bone marrow cells from animals treated with cell-free filtrates contained numerous cylindrical inclusions, several of which demonstrated viral budding. Complement fixation and mouse embryo cytopathogenicity tests on tumor extracts identified the viral particles as members of the murine leukemia-sarcoma group and demonstrated high titers of infectivity.

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Publisher
American Association of Cancer Research
Copyright
Copyright © 1973 by the American Association for Cancer Research.
ISSN
0008-5472
Publisher site

Abstract

C-type viruses were identified by electron microscopy in muramidase-producing transplantable leukemic cells of BALB/c mice. Neoplastic cells contained peroxidase-positive cytoplasmic granules and consisted of atypical monocytic and granulocytic precursors, undifferentiated stem cells, and histiocytes. Viral particles were present in all tumors studied and were principally of the intracisternal A and immature C types. Exceptionally, mature C-type virions were noted in large cytoplasmic vacuoles of tumor cells, in bone marrow megakaryocytes, and in extracellular spaces. Unusual cytoplasmic structures that may represent structural precursors of viral nucleoprotein assembly were also observed in some cells. Bone marrow cells from animals treated with cell-free filtrates contained numerous cylindrical inclusions, several of which demonstrated viral budding. Complement fixation and mouse embryo cytopathogenicity tests on tumor extracts identified the viral particles as members of the murine leukemia-sarcoma group and demonstrated high titers of infectivity.

Journal

Cancer ResearchAmerican Association of Cancer Research

Published: Apr 1, 1973

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