Efficient B Cell Depletion via Diphtheria Toxin in CD19-Cre/iDTR Mice

Filiz Demircik, Thorsten Buch, Ari Waisman

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

B cells were first discovered as antibody producing cells, as B-1 B cells and finally as effector cells. In recent years their capacity to serve as antigen presenting cells is increasingly appreciated, and better tools are needed to study their function. We have previously described a new mouse model, the iDTR mice, that allow for the Cre-mediated expression of the diphtheria toxin receptor, thus rendering cells that express the Cre-recombinase sensitivity to diphtheria toxin. Herein we describe a new mouse line, the B-DTR mice, where the CD19-Cre was crossed to the iDTR mice. B-DTR allows for the efficient and cost-effective depletion of different B cell subpopulations, but only partially plasma cells. These mice can therefore be used to study the importance of B cells versus plasma cells in different immune responses and autoimmune diseases.

Original languageEnglish
Article numbere60643
JournalPLoS ONE
Volume8
Issue number3
DOIs
StatePublished - 27 Mar 2013

Fingerprint

Dive into the research topics of 'Efficient B Cell Depletion via Diphtheria Toxin in CD19-Cre/iDTR Mice'. Together they form a unique fingerprint.

Cite this