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Cooperation of ETV6/RUNX1 and BCL2 enhances immunoglobulin production and accelerates glomerulonephritis in transgenic mice

Authors :
Dagmar Stoiber
Jaqueline Horvath
Renate Kain
Gregor Hoermann
Ruth Scheicher
Ana-Iris Schiefer
Petra Aigner
Lukas Kenner
Michaela Schlederer
Günter Steiner
Heinz Regele
Andreas Villunger
Richard Moriggl
Eva Bauer
Veronika Sexl
Source :
Oncotarget
Publication Year :
2016
Publisher :
Impact Journals, LLC, 2016.

Abstract

// Eva Bauer 1 , Michaela Schlederer 1,2 , Ruth Scheicher 3 , Jaqueline Horvath 1,4 , Petra Aigner 1 , Ana-Iris Schiefer 2 , Renate Kain 2 , Heinz Regele 2 , Gregor Hoermann 5 , Gunter Steiner 6,7 , Lukas Kenner 1,2,8 , Veronika Sexl 3 , Andreas Villunger 9,10 , Richard Moriggl 1,5,11 and Dagmar Stoiber 1,4 1 Ludwig Boltzmann Institute for Cancer Research, Vienna, Austria 2 Clinical Institute of Pathology, Medical University of Vienna, Vienna, Austria 3 Institute of Pharmacology and Toxicology, University of Veterinary Medicine, Vienna, Austria 4 Institute of Pharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria 5 Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria 6 Cluster Arthritis and Rehabilitation, Ludwig Boltzmann Society, Vienna, Austria 7 Division of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria 8 Unit of Pathology of Laboratory Animals, University of Veterinary Medicine, Vienna, Austria 9 Division of Developmental Immunology, Biocenter, Medical University Innsbruck, Innsbruck, Austria 10 Tyrolean Cancer Research Institute, Innsbruck, Austria 11 Institute of Animal Breeding and Genetics, University of Veterinary Medicine, Vienna, Austria Correspondence to: Dagmar Stoiber, email: // Keywords : ETV6/RUNX1, BCL2, glomerulonephritis, lymphoma, autoimmunity, Immunology and Microbiology Section, Immune response, Immunity Received : September 11, 2015 Accepted : January 31, 2016 Published : February 23, 2016 Abstract The t(12;21) translocation generating the ETV6/RUNX1 fusion gene represents the most frequent chromosomal rearrangement in childhood leukemia. Presence of ETV6/RUNX1 alone is usually not sufficient for leukemia onset, and additional genetic alterations have to occur in ETV6/RUNX1-positive cells to cause transformation. We have previously generated an ETV6/RUNX1 transgenic mouse model where the expression of the fusion gene is restricted to CD19-positive B cells. Since BCL2 family members have been proposed to play a role in leukemogenesis, we investigated combined effects of ETV6/RUNX1 with exogenous expression of the antiapoptotic protein BCL2 by crossing ETV6/RUNX1 transgenic animals with Vav-BCL2 transgenic mice. Strikingly, co-expression of ETV6/RUNX1 and BCL2 resulted in significantly shorter disease latency in mice, indicating oncogene cooperativity. This was associated with faster development of follicular B cell lymphoma and exacerbated immune complex glomerulonephritis. ETV6/RUNX1-BCL2 double transgenic animals displayed increased B cell numbers and immunoglobulin titers compared to Vav-BCL2 transgenic mice. This led to pronounced deposition of immune complexes in glomeruli followed by accelerated development of immune complex glomerulonephritis. Thus, our study reveals a previously unrecognized synergism between ETV6/RUNX1 and BCL2 impacting on malignant disease and autoimmunity.

Details

ISSN :
19492553
Volume :
7
Database :
OpenAIRE
Journal :
Oncotarget
Accession number :
edsair.doi.dedup.....71fa804c9bd585d04983a16e5c79a423