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Induction of sterile transcription from the kL chain gene locus in V(D)J recombinasedeficient progenitor B cells

Grawunder, Ulf ; Rolink, Antonius ; Melchers, Fritz

In: International Immunology, 1995, vol. 7, no. 12, p. 1915-1925

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    Titel
    • Induction of sterile transcription from the kL chain gene locus in V(D)J recombinasedeficient progenitor B cells
    Autor
    • Grawunder, Ulf. Washington University School of Medicine, Division of Molecular Oncology, Department of Pathology, Medicine and Biochemistry St Louis, MO 63110, USA
    • Rolink, Antonius. Basel Institute for Immunology, Grenzacherstrasse 487, 4005 Basel, Switzerland, St Louis, MO 63110, USA
    • Melchers, Fritz. Basel Institute for Immunology, Grenzacherstrasse 487, 4005 Basel, Switzerland, St Louis, MO 63110, USA
    Dokumententyp
    • Postprint
    Sprache
    • Englisch
    Veröffentlicht in
    • International Immunology, 1995, vol. 7, no. 12, p. 1915-1925. Oxford University Press
    Andere elektronische Ausgabe
    OAI-PMH-ID
    • oai:doc.rero.ch:301509
    Summary
    B cell development in RAG-2-deficient (RAG-2T) mice is impeded at an early stage, due to the inability of these animals to rearrange their endogenous lg gene loci. Expression of an Eμ-bci-2 transgene in these mice did not change this phenotype. However, stromal cell/IL-7-reactive B cell progenitors (pro-B cells) were found in fetal liver and bone marrow of RAG-2T and RAG-2T/Eμ-bci-2 transgenic mice in numbers comparable to normal mice. Like cells from normal mice they are c-kit+, surrogate L chain+ and CD25−, and can proliferate in vitro for long periods of time. Upon IL-7 deprivation, they can be induced to differentiate into c-kit−, surrogate L chain+ and CD25− cells that are no longer clonable on stromal cells and IL-7. Furthermore, sterile transcription from the kL.chain gene loci is induced. The latter was also observed with pro-B cells directly isolated ex vivo from the bone marrow of RAG-2-deficient animals. The results suggest that progenitor B celldifferentiation can occur in cells from V(D)J recombinase-deficient mice to the stage where KL chain gene rearrangements would normally be initiated. It further indicates that some molecular programs of early B cell differentiation can take place in the absence of lg gene rearrangements