Long-lived polyclonal B-cell lines derived from midgestation mouse embryo lymphohematopoietic progenitors reconstitute adult immunodeficient mice

Lymphohematopoietic progenitors derived from midgestation mouse embryos were established in long-term cultures with stromal cell monolayers and interleukin 7 (IL-7), giving rise to B-lineage cell lines. The initial emergence and in vitro establishment of these early embryo cell lines were highly sen...

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Bibliographic Details
Published in:Blood Vol. 98; no. 6; pp. 1862 - 1871
Main Authors: Martı́nez-M., José A., Minguet, Susana, Gonzalo, Pilar, Soro, Pilar G., de Andrés, Belén, Ízcue, Ana, Marcos, Miguel A.R., Gaspar, Marı́a-Luisa
Format: Journal Article
Language:English
Published: Washington, DC Elsevier Inc 15-09-2001
The Americain Society of Hematology
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Summary:Lymphohematopoietic progenitors derived from midgestation mouse embryos were established in long-term cultures with stromal cell monolayers and interleukin 7 (IL-7), giving rise to B-lineage cell lines. The initial emergence and in vitro establishment of these early embryo cell lines were highly sensitive to IL-7–mediated signals, in comparison to cell lines similarly obtained using precursors from late fetal liver (> 13 days postcoitum) and adult bone marrow. The early embryo-derived progenitors spontaneously differentiated in vitro to CD19+IgM+ immature B cells in the presence of optimal concentrations of IL-7, in contrast to those progenitors obtained from late gestation and adult mice, whose differentiation only occurred in the absence of IL-7. The newly in vitro–generated B cells of the early embryo cell lines repopulated adult immunodeficient severe combined immunodeficient mice on their adoptive transfer in vivo and generated specific humoral immune responses after immunization.
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ISSN:0006-4971
1528-0020
DOI:10.1182/blood.V98.6.1862