Source:http://linkedlifedata.com/resource/pubmed/id/11929764
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2002-4-3
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pubmed:abstractText |
Self-renewal, pluripotency, and long-term reconstitution are defining characteristics of single hematopoietic stem cells. Pax5(-/-) precursor B cells apparently possess similar characteristics. Here, using serial transplantations, with in vitro recloning and growth of the bone marrow-homed donor cells occurring after all transplantations, we analyzed the extent of self-renewal and hematopoietic multipotency of Pax5(-/-) precursor B-cell clones. Moreover, telomere length and telomerase activity in these clones was analyzed at various time points. Thus far, 5 successive transplantations have been performed. Clones transplanted for the fifth time, which have proliferated for more than 150 cell divisions in vitro, still repopulate the bone marrow with precursor B cells and reconstitute these recipients with lymphoid and myeloid cells. During this extensive proliferation, Pax5(-/-) precursor B cells shorten their telomeres at 70 to 90 base pairs per division. Their telomerase activity remains at 3% of that of HEK293 cancer cells during all serial in vivo transplantations/in vitro expansions. Together, these data show that Pax5(-/-) precursor B-cell clones possess extensive in vivo self-renewal capacity, long-term reconstitution capacity, and hematopoietic multipotency, with their telomeres shortening at the normal rate.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/B-Cell-Specific Activator Protein,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Pax5 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0006-4971
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
99
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2760-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11929764-Animals,
pubmed-meshheading:11929764-B-Cell-Specific Activator Protein,
pubmed-meshheading:11929764-B-Lymphocytes,
pubmed-meshheading:11929764-Bone Marrow,
pubmed-meshheading:11929764-Cell Differentiation,
pubmed-meshheading:11929764-Cell Division,
pubmed-meshheading:11929764-Cell Movement,
pubmed-meshheading:11929764-Clone Cells,
pubmed-meshheading:11929764-DNA-Binding Proteins,
pubmed-meshheading:11929764-Hematopoiesis,
pubmed-meshheading:11929764-Hematopoietic Stem Cell Transplantation,
pubmed-meshheading:11929764-Hematopoietic Stem Cells,
pubmed-meshheading:11929764-Mice,
pubmed-meshheading:11929764-Mice, Knockout,
pubmed-meshheading:11929764-Telomere,
pubmed-meshheading:11929764-Transcription Factors
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pubmed:year |
2002
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pubmed:articleTitle |
Extensive in vivo self-renewal, long-term reconstitution capacity, and hematopoietic multipotency of Pax5-deficient precursor B-cell clones.
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pubmed:affiliation |
Basel Institute for Immunology, Switzerland. schaniel@molbio.princeton.edu
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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