Evidence map›Paper›PMID 32755576›Full record

ArticleCell reports2020

Stromal Cell-Contact Dependent PI3K and APRIL Induced NF-κB Signaling Prevent Mitochondrial- and ER Stress Induced Death of Memory Plasma Cells.

Rebecca Cornelis, Stefanie Hahne, Adriano Taddeo, Georg Petkau, Darya Malko, Pawel Durek, Manja Thiem, Lukas Heiberger, Lena Peter, Elodie Mohr and 9 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Why are long-lived plasma cells long-lived?Frontiers in immunology · 2026
    Review
  3. The inflammatory clock: how cGAS-STING ticks in the aging ovary.Frontiers in cell and developmental biology · 2026
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 2 institutions in 1 country.

Rebecca CornelisDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Stefanie HahneDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Adriano TaddeoDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Georg PetkauDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Darya MalkoDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Pawel DurekDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Manja ThiemDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Lukas HeibergerDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Lena PeterDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Elodie MohrDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Cora KlaedenDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Koji TokoyodaDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Francesco SiracusaDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Bimba Franziska HoyerDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany; Charité-Universitätsmedizin Berlin, Department of Rheumatology and Clinical Immunology, 10117 Berlin, Germany.
Falk HiepeDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany; Charité-Universitätsmedizin Berlin, Department of Rheumatology and Clinical Immunology, 10117 Berlin, Germany.
Mir-Farzin MashreghiDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Fritz MelchersDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Hyun-Dong ChangDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany.
Andreas RadbruchDeutsches Rheuma-Forschungszentrum Berlin (DRFZ), a Leibniz Institute, Chariteplatz1, 10117 Berlin, Germany. Electronic address: radbruch@drfz.de.
German Rheumatism Research Centre · DECharité - Universitätsmedizin Berlin · DE

Funding

European Research Council 268987
6 · The paper itself

Abstract

The persistence of long-lived memory plasma cells in the bone marrow depends on survival factors available in the bone marrow, which are provided in niches organized by stromal cells. Using an ex vivo system in which we supply the known survival signals, direct cell contact to stromal cells, and the soluble cytokine a proliferation-inducing ligand (APRIL), we have elucidated the critical signaling pathways required for the survival of long-lived plasma cells. Integrin-mediated contact of bone marrow plasma cells with stromal cells activates the phosphatidylinositol 3-kinase (PI3K) signaling pathway, leading to critical inactivation of Forkhead-Box-Protein O1/3 (FoxO1/3) and preventing the activation of mitochondrial stress-associated effector caspases 3 and 7. Accordingly, inhibition of PI3K signaling in vivo ablates bone marrow plasma cells. APRIL signaling, by the nuclear factor κB (NF-κB) pathway, blocks activation of the endoplasmic-reticulum-stress-associated initiator caspase 12. Thus, stromal-cell-contact-induced PI3K and APRIL-induced NF-κB signaling provide the necessary and complementary signals to maintain bone marrow memory plasma cells.

Indexed as

Endoplasmic Reticulum StressImmunologic MemoryAnimalsBone Marrow CellsCaspasesCell DeathCell SurvivalDown-RegulationForkhead Box Protein O1Forkhead Box Protein O3Interferon Regulatory Factor-4Interferon Regulatory FactorsMice, Inbred C57BLMitochondriaNF-kappa BPhosphatidylinositol 3-KinaseCaspasesForkhead Box Protein O1Forkhead Box Protein O3Interferon Regulatory Factor-4Interferon Regulatory FactorsNF-kappa BPhosphatidylinositol 3-KinaseTnfsf13 protein, mouseTumor Necrosis Factor Ligand Superfamily Member 13APRILBCMAbone marrowcaspase 12caspase 3caspase 7FoxOIRF4long-lived memory PCsPI3K/AKTstromal cell

Identifiers

PMID32755576
PMCPMC7408492
OpenAlexW3046935924

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.