Skip to Content
Merck
CN
  • The development of functional B lymphocytes in conditional PU.1 knock-out mice.

The development of functional B lymphocytes in conditional PU.1 knock-out mice.

Blood (2005-06-04)
Matthew Polli, Aleksandar Dakic, Amanda Light, Li Wu, David M Tarlinton, Stephen L Nutt
ABSTRACT

An abundance of research has entrenched the view that the Ets domain containing transcription factor PU.1 is fundamental to the development and function of B lymphocytes. In this study, we have made use of a conditional PU.1 allele to test this notion. Complete deletion of PU.1 resulted in the loss of B cells and all other lineage-positive cells in the fetal liver and death between E18.5 and birth; however, specific deletion of PU.1 in the B lineage had no effect on B-cell development. Furthermore, deletion of PU.1 in B cells did not compromise their ability to establish and maintain an immune response. An increased level of apoptosis was observed in vitro upon B-cell receptor (BCR) cross-linking; however, this was partially rescued by interleukin-4 (IL-4). These findings suggest that PU.1 is not essential for the development of functional B lymphocytes beyond the pre-B stage.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
IgM, Kappa from murine myeloma, clone TEPC 183, purified immunoglobulin, buffered aqueous solution
Sigma-Aldrich
Mouse IgG2a Isotype Control from murine myeloma, clone UPC-10, purified immunoglobulin, buffered aqueous solution
Sigma-Aldrich
Mouse IgG1-k Negative Control, clone MOPC-21, Azide Free Antibody, clone MOPC-21, from mouse