Early B-cell precursors in scid mice: Normal numbers of cells transformable with abelson murine leukemia virus (A-MuLV)
scid mice lack detectable B and T lymphocytes; there are no typical pre-B cells as defined by cμ and surface markers in their bone marrow and their thymus contains only 1% of the normal number of cells. In these characters scid mice seem to lack lymphoid stem cells. However, some mice have detectabl...
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Published in | Cellular immunology Vol. 113; no. 1; pp. 192 - 201 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
San Diego, CA
Elsevier Inc
15.04.1988
Elsevier |
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Abstract | scid mice lack detectable B and T lymphocytes; there are no typical pre-B cells as defined by cμ and surface markers in their bone marrow and their thymus contains only 1% of the normal number of cells. In these characters
scid mice seem to lack lymphoid stem cells. However, some mice have detectable serum immunoglobulin and others develop thymomas; both observations indicate that the block in lymphoid development is not absolute. To determine whether
scid mice have any B-cell precursors, we looked for pre-B cells by their ability to be transformed by Abelson murine leukemia virus (A-MuLV). Surprisingly,
scid mice contain as many B-cell precursors transformable with A-MuLV as normal control mice. Cell-surface markers specific for pre-B and B cells were detected on the A-MuLV-transformed bone marrow cells of both
scid and normal mice, indicating that the A-MuLV-transformed cells belong to the B lineage. Interestingly, the same surface markers were undetectable on nontransformed
scid bone marrow cells. We conclude from these results that
scid mice have normal numbers of early B-cell precursors but that their differentiation into functional B cells is severely impaired. |
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AbstractList | scid mice lack detectable B and T lymphocytes; there are no typical pre-B cells as defined by c mu and surface markers in their bone marrow and their thymus contains only 1% of the normal number of cells. In these characters scid mice seem to lack lymphoid stem cells. However, some mice have detectable serum immunoglobulin and others develop thymomas; both observations indicate that the block in lymphoid development is not absolute. To determine whether scid mice have any B-cell precursors, we looked for pre-B cells by their ability to be transformed by Abelson murine leukemia virus (A-MuLV). Surprisingly, scid mice contain as many B-cell precursors transformable with A-MuLV as normal control mice. Cell-surface markers specific for pre-B and B cells were detected on the A-MuLV-transformed bone marrow cells of both scid and normal mice, indicating that the A-MuLV-transformed cells belong to the B lineage. Interestingly, the same surface markers were undetectable on nontransformed scid bone marrow cells. We conclude from these results that scid mice have normal numbers of early B-cell precursors but that their differentiation into functional B cells is severely impaired. scid mice lack detectable B and T lymphocytes; there are no typical pre-B cells as defined by cμ and surface markers in their bone marrow and their thymus contains only 1% of the normal number of cells. In these characters scid mice seem to lack lymphoid stem cells. However, some mice have detectable serum immunoglobulin and others develop thymomas; both observations indicate that the block in lymphoid development is not absolute. To determine whether scid mice have any B-cell precursors, we looked for pre-B cells by their ability to be transformed by Abelson murine leukemia virus (A-MuLV). Surprisingly, scid mice contain as many B-cell precursors transformable with A-MuLV as normal control mice. Cell-surface markers specific for pre-B and B cells were detected on the A-MuLV-transformed bone marrow cells of both scid and normal mice, indicating that the A-MuLV-transformed cells belong to the B lineage. Interestingly, the same surface markers were undetectable on nontransformed scid bone marrow cells. We conclude from these results that scid mice have normal numbers of early B-cell precursors but that their differentiation into functional B cells is severely impaired. scid mice lack detectable B and T lymphocytes; there are no typical pre-B cells as defined by c mu and surface markers in their bone marrow and their thymus contains only 1% of the normal number of cells. In these characters scid mice seem to lack lymphoid stem cells. To determine whether scid mice have any B-cell precursors, the authors looked for pre-B cells by their ability to be transformed by Abelson murine leukemia virus (A-MuLV). They conclude from the results that scid mice have normal numbers of early B-cell precursors but that their differentiation into functional B cells is severely impaired. |
Author | Bosma, G.C. Phillips, R.A. Fulop, G.M. Bosma, M.J. |
Author_xml | – sequence: 1 givenname: G.M. surname: Fulop fullname: Fulop, G.M. organization: Department of Medical Biophysics, University of Toronto, and Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, Canada – sequence: 2 givenname: G.C. surname: Bosma fullname: Bosma, G.C. organization: The Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania, U.S.A – sequence: 3 givenname: M.J. surname: Bosma fullname: Bosma, M.J. organization: The Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania, U.S.A – sequence: 4 givenname: R.A. surname: Phillips fullname: Phillips, R.A. organization: Department of Medical Biophysics, University of Toronto, and Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, Canada |
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Cites_doi | 10.1084/jem.153.2.269 10.1038/289681a0 10.1016/0092-8674(79)90014-X 10.1038/301527a0 10.1016/S0065-2776(08)60338-7 10.4049/jimmunol.138.8.2698 10.4049/jimmunol.128.6.2793 10.1007/BF00372098 10.4049/jimmunol.130.2.644 10.4049/jimmunol.136.12.4438 10.1084/jem.145.6.1567 10.1084/jem.143.6.1453 10.1016/0092-8674(81)90421-9 10.1002/eji.1830150613 10.4049/jimmunol.127.6.2262 10.1016/0092-8674(86)90695-1 10.1016/S0065-2660(08)60549-0 |
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Keywords | Cell culture Flow cytometry Immunopathology Oncovirinae Rodentia Retroviridae B-Lymphocyte Indirect immunofluorescence Cell transformation Precursor Cell surface Virus Antigen Vertebrata Mammalia Mouse Type C oncovirus Bone marrow Murine leukemia virus Severe Combined immune deficiency |
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Immunol doi: 10.4049/jimmunol.127.6.2262 contributor: fullname: Kincade – volume: 46 start-page: 963 year: 1986 ident: 10.1016/0008-8749(88)90017-2_BIB20 publication-title: Cell doi: 10.1016/0092-8674(86)90695-1 contributor: fullname: Schuler – volume: 20 start-page: 357 year: 1979 ident: 10.1016/0008-8749(88)90017-2_BIB24 publication-title: Adv. Genet doi: 10.1016/S0065-2660(08)60549-0 contributor: fullname: Russell |
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Snippet | scid mice lack detectable B and T lymphocytes; there are no typical pre-B cells as defined by cμ and surface markers in their bone marrow and their thymus... scid mice lack detectable B and T lymphocytes; there are no typical pre-B cells as defined by c mu and surface markers in their bone marrow and their thymus... |
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SubjectTerms | Abelson murine leukemia virus Animals B-Lymphocytes - immunology Biological and medical sciences Bone Marrow - immunology Bone Marrow - pathology Cell Line, Transformed Cell Transformation, Viral Experimental and animal immunopathology. Animal models Hematopoietic Stem Cells - immunology Immunologic Deficiency Syndromes - genetics Immunologic Deficiency Syndromes - immunology Immunologic Deficiency Syndromes - pathology Immunopathology Leukemia Virus, Murine Leukocyte Count Lymphocyte Activation Medical sciences Mice Mice, Inbred BALB C Mice, Mutant Strains - immunology |
Title | Early B-cell precursors in scid mice: Normal numbers of cells transformable with abelson murine leukemia virus (A-MuLV) |
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