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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
1993-6-1
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pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S55623,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S55625,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S55628,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S55677,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S55678,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S55680,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S55739,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S59838,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S59883,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S65854
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pubmed:abstractText |
AKR mice are highly susceptible to development of spontaneous T-cell lymphoma. Thymus removal at the age of 1-3 months greatly reduces T-cell lymphoma. Lymphomas that have the characteristics of T- and/or B-cells occur sporadically in peripheral lymphoid tissues of old thymectomized AKR/J mice. These thymectomized mice were shown to carry dormant potential lymphoma cells. Transplantation of lymphoid cells from 8-12-month-old AKR/J mice, thymectomized at the age of 6 to 8 weeks, into intact or thymectomized young recipients yielded 80-100% Ly-1+ pre-B or B-cell lymphomas. In the AKR-Fv-1b congenic strain the Fv-1n allele of AKR/J mice was substituted with the Fv-1b allele, thereby limiting viral replication and spread of the endogenous N-tropic murine leukemia virus. As a result of this restriction in virus spread, AKR-Fv-1b mice develop a low spontaneous incidence (7%) of T-cell lymphomas and about 28% of Ly-1+ B-cell lymphomas at old age. In spleens of 15-18-month-old thymectomized AKR/J mice and intact AKR-Fv-1b mice, 30-60% of the B-cells were of the Ly-1+ B type. Analysis of the IgH locus in these normal old spleens and Ly-1+ B lymphomas indicated mono- or oligoclonality. One particular IgH rearrangement was identified in many individual old spleens and tumors. A second specific IgH rearrangement was found in some tumors. Possible mechanisms involved in the expansion of Ly-1+ clones and their progression into tumors are discussed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0008-5472
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
|
pubmed:volume |
53
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
2147-53
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7683252-Age Factors,
pubmed-meshheading:7683252-Animals,
pubmed-meshheading:7683252-Antigens, CD,
pubmed-meshheading:7683252-Antigens, CD5,
pubmed-meshheading:7683252-Antigens, Ly,
pubmed-meshheading:7683252-B-Lymphocyte Subsets,
pubmed-meshheading:7683252-Base Sequence,
pubmed-meshheading:7683252-Blotting, Southern,
pubmed-meshheading:7683252-Clone Cells,
pubmed-meshheading:7683252-Gene Rearrangement, B-Lymphocyte, Heavy Chain,
pubmed-meshheading:7683252-Genes, Immunoglobulin,
pubmed-meshheading:7683252-Lymphoma,
pubmed-meshheading:7683252-Mice,
pubmed-meshheading:7683252-Mice, Inbred AKR,
pubmed-meshheading:7683252-Molecular Sequence Data,
pubmed-meshheading:7683252-Spleen,
pubmed-meshheading:7683252-Thymectomy
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pubmed:year |
1993
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pubmed:articleTitle |
Analysis of Ly-1+ B-cell populations and IgH rearrangements in "normal" spleens and in lymphomas of AKR/J and AKR Fv-1b mice.
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pubmed:affiliation |
Department of Chemical Immunology, Weizmann Institute of Science, Rehovot, Israel.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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