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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1996-5-29
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pubmed:abstractText |
Peripheral blood mononuclear cells from five patients with IgG+ B-type chronic lymphocytic leukemia (B-CLL) were analyzed for the presence of clone-specific Ig H chain variable region gene mRNA transcripts linked to C mu and/or C alpha. This was assessed by (1) comparing the lengths of portions of the VHDJH of the IgG+ CLL clones with those of the mu and alpha isotype-expressing B cells, (2) performing clone-specific endonuclease digestion studies, and (3) determining the DNA sequences of the mu and alpha isotype-expressing cDNA. Thus, when B-cell mRNA from these five patients were reverse transcribed with C gamma-specific primers and then amplified by polymerase chain reaction, dominant cDNA were found with lengths corresponding to those of the IgG+ CLL B cell. In addition, in four cases, cDNA of lengths identical to those of the CLL B cell were detected when mRNA was reverse transcribed and amplified using c mu- and/or C alpha-specific primers, strongly suggesting clonal relatedness. These CLL-related mu- and alpha-expressing cDNA were present in greater amounts that unrelated (non-CLL) mu- and alpha-expressing cDNA from normal B cells that used genes of the same VH family. When the sequences of these CLL-related C mu- and C alpha-expressing cDNA were compared with those of the IgG+ CLL clones, it was clear that they were derived from the same ancestral gene as the IgG-expressing CLL B cell, thus documenting their common origin. Finally, nucleotide point mutations were observed in the mu- and alpha-expressing cDNA of certain patients, indicating divergence with the CLL. These data suggest that IgM+ B cells, which are precursors of the leukemic B cells, exist in increased numbers in the blood of most patients with IgG+ B-CELL and that these cells may differentiate, accumulate V genes mutations, and undergo isotype switching in vivo. In addition, the data are consistent with a sequential-hit model for the evolution of CLL.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0006-4971
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pubmed:author |
pubmed-author:AllenS LSL,
pubmed-author:ChiorazziNN,
pubmed-author:DongEE,
pubmed-author:FainCC,
pubmed-author:FerrariniMM,
pubmed-author:GregersenP KPK,
pubmed-author:HashimotoSS,
pubmed-author:LichtmanS MSM,
pubmed-author:SchulmanPP,
pubmed-author:SellarsBB,
pubmed-author:TrejoVV,
pubmed-author:VinciguerraV PVP
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pubmed:issnType |
Print
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pubmed:day |
15
|
pubmed:volume |
87
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1586-94
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:8608251-Base Sequence,
pubmed-meshheading:8608251-Cell Differentiation,
pubmed-meshheading:8608251-Clone Cells,
pubmed-meshheading:8608251-DNA Primers,
pubmed-meshheading:8608251-Gene Rearrangement, B-Lymphocyte,
pubmed-meshheading:8608251-Genes, Immunoglobulin,
pubmed-meshheading:8608251-Humans,
pubmed-meshheading:8608251-Immunoglobulin alpha-Chains,
pubmed-meshheading:8608251-Immunoglobulin mu-Chains,
pubmed-meshheading:8608251-Leukemia, Lymphocytic, Chronic, B-Cell,
pubmed-meshheading:8608251-Molecular Sequence Data,
pubmed-meshheading:8608251-RNA, Messenger,
pubmed-meshheading:8608251-Sequence Alignment,
pubmed-meshheading:8608251-Sequence Homology, Nucleic Acid,
pubmed-meshheading:8608251-Transcription, Genetic
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pubmed:year |
1996
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pubmed:articleTitle |
Evidence for progenitors of chronic lymphocytic leukemia B cells that undergo intraclonal differentiation and diversification.
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pubmed:affiliation |
Department of Medicine, North Shore University Hospital, Manhasset, NY 11030, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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