PDGFA-associated protein 1 protects mature B lymphocytes from stress-induced cell death and promotes antibody gene diversification

Author:

Delgado-Benito Verónica1,Berruezo-Llacuna Maria1,Altwasser Robert12,Winkler Wiebke34,Sundaravinayagam Devakumar1,Balasubramanian Sandhya1,Caganova Marieta3ORCID,Graf Robin3ORCID,Rahjouei Ali1,Henke Marie-Thérèse5,Driesner Madlen1,Keller Lisa1,Prigione Alessandro56ORCID,Janz Martin4,Akalin Altuna2,Di Virgilio Michela17ORCID

Affiliation:

1. Laboratory of Genome Diversification and Integrity, Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany

2. Bioinformatics and Omics Data Science Technology Platform, Berlin Institute of Medical Systems Biology, Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany

3. Laboratory of Immune Regulation and Cancer, Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany

4. Laboratory of Biology of Malignant Lymphomas, Experimental and Clinical Research Center, Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité, University Medicine, Berlin, Germany

5. Laboratory of Mitochondria and Cell Fate Reprogramming, Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany

6. Department of General Pediatrics, Neonatology and Pediatric Cardiology, University Children’s Hospital, Heinrich Heine University, Düsseldorf, Germany

7. Charité-Universitätsmedizin Berlin, Berlin, Germany

Abstract

The establishment of protective humoral immunity is dependent on the ability of mature B cells to undergo antibody gene diversification while adjusting to the physiological stressors induced by activation with the antigen. Mature B cells diversify their antibody genes by class switch recombination (CSR) and somatic hypermutation (SHM), which are both dependent on efficient induction of activation-induced cytidine deaminase (AID). Here, we identified PDGFA-associated protein 1 (Pdap1) as an essential regulator of cellular homeostasis in mature B cells. Pdap1 deficiency leads to sustained expression of the integrated stress response (ISR) effector activating transcription factor 4 (Atf4) and induction of the ISR transcriptional program, increased cell death, and defective AID expression. As a consequence, loss of Pdap1 reduces germinal center B cell formation and impairs CSR and SHM. Thus, Pdap1 protects mature B cells against chronic ISR activation and ensures efficient antibody diversification by promoting their survival and optimal function.

Funder

European Research Council

Helmholtz-Gemeinschaft

Deutsche Krebshilfe

Helmholtz Association

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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