Lymphoproliferative disorders in IL-7 transgenic mice: Expansion of immature B cells which retain macrophage potential

  • A. G. Fisher
  • , C. Burdet
  • , C. Bunce
  • , M. Merkenschlager
  • , Rh Ceredig

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

66 Citations (Scopus)

Abstract

Transgenic mice carrying the murine IL-7 gene under the MHC class II (Eα) promoter are described which develop lymphoid tumours at a high incidence when maintained in conventional or specific pathogen-free environments. Cells obtained from the lesions were relatively monomorphic, expressed a variety of B cell associated markers (BP-1, B220, CD43) but lacked surface Ig. Some mice showed expanded populations of cells phenotypically similar to the recently reported bipotent B/macrophage stem cell subset (AA4.1high, B220-, Ig-) which could be cloned and maintained in vitro. These cells expressed IL-7 receptors, proliferated in response to IL-7 and in most cases had germllne configuration of the Ig heavy chain locus. Cell lines cloned from two such tumours generated macrophages spontaneously in culture, consistent with their bipotent B cell/macrophage phenotype. These results suggest that IL-7 plays a role in very early stages of B cell ontogeny prior to bona fide B cell commitment.

Original languageEnglish
Pages (from-to)415-423
Number of pages9
JournalInternational Immunology
Volume7
Issue number3
DOIs
Publication statusPublished - Mar 1995
Externally publishedYes

Keywords

  • B cell
  • IL-7
  • Lymphoproliferative disorder
  • Macrophage

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