Evidence map›Paper›PMID 33148712›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2020

AMPKα1 in B Cells Dampens Primary Antibody Responses yet Promotes Mitochondrial Homeostasis and Persistence of B Cell Memory.

Shawna K Brookens, Sung Hoon Cho, Paulo J Basso, Mark R Boothby

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Review
  2. A guide to B cell metabolism.Nature reviews. Immunology · 2026
    Review
  3. Article
  4. Review
  5. Review
  6. Multifaceted roles of mitochondria in asthma.Cell biology and toxicology · 2024
    Review
  7. The influence of metabolic disorders on adaptive immunity.Cellular & molecular immunology · 2024
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review
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

4 authors.

Shawna K BrookensDepartment of Cancer Biology, Vanderbilt University, Nashville, TN 37232.ORCID 0000-0003-1620-6276
Sung Hoon ChoDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232; and.
Paulo J BassoDepartment of Immunology, University of São Paulo, São Paulo 05508-000, Brazil.
Mark R BoothbyDepartment of Cancer Biology, Vanderbilt University, Nashville, TN 37232; mark.boothby@vumc.org.

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
Vanderbilt/Meharry Initiative for Minority Student DvptR25GM062459 · NIGMS · VANDERBILT UNIVERSITY · PI VELEZ EDWARDS, DIGNA R · 2002 to 2020
$10.4M
MULTIDISCIPLINARY BASIC RESEARCH TRAINING IN CANCERT32CA009592 · NCI · VANDERBILT UNIVERSITY · PI Justin M Balko, Julie A Rhoades (Sterling) · 1987 to 2026
$10.4M
Roles of rictor in mTOR signaling, differentiation & immune memory via Akt & PKCR01HL106812 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BOOTHBY, MARK R · 2011 to 2018
$3.1M
Fit to remember? B cell metabolic 'fitness', AMPK & recall antibody responsesR01AI113292 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BOOTHBY, MARK R · 2015 to 2019
$1.9M
Fit to remember? B cell metabolic 'fitness', AMPK & recall antibody responsesR56AI113292 · NIAID · VANDERBILT UNIVERSITY · PI BOOTHBY, MARK R · 2014 to 2014
$393k
XFe96 AnalyzerS10OD018015 · OD · VANDERBILT UNIVERSITY · PI LANNIGAN, DEBORAH · 2014 to 2014
$200k
NCI NIH HHS P30 CA068485NCI NIH HHS T32 CA009592NHLBI NIH HHS R01 HL106812NIAID NIH HHS R01 AI113292NIAID NIH HHS R56 AI113292NIGMS NIH HHS R25 GM062459NIH HHS S10 OD018015
6 · The paper itself

Abstract

Emerging evidence indicates that metabolic programs regulate B cell activation and Ab responses. However, the metabolic mediators that support the durability of the memory B cell and long-lived plasma cell populations are not fully elucidated. Adenosine monophosphate-activated protein kinase (AMPK) is an evolutionary conserved serine/threonine kinase that integrates cellular energy status and nutrient availability to intracellular signaling and metabolic pathways. In this study, we use genetic mouse models to show that loss of ΑMPKα1 in B cells led to a weakened recall Ab response associated with a decline in the population of memory-phenotype B cells. AMPKα1-deficient memory B lymphocytes exhibited aberrant mitochondrial activity, decreased mitophagy, and increased lipid peroxidation. Moreover, loss of AMPKα1 in B lymphoblasts was associated with decreased mitochondrial spare respiratory capacity. Of note, AMPKα1 in B cells was dispensable for stability of the bone marrow-resident, long-lived plasma cell population, yet absence of this kinase led to increased rates of Ig production and elevated serum Ab concentrations elicited by primary immunization. Collectively, our findings fit a model in which AMPKα1 in B cells supports recall function of the memory B cell compartment by promoting mitochondrial homeostasis and longevity but restrains rates of Ig production.

Indexed as

AMP-Activated Protein KinasesAnimalsAntibodiesAntibody FormationB-LymphocytesBone MarrowFemaleHomeostasisImmunizationImmunoglobulinsImmunologic MemoryLipid PeroxidationMaleMiceMitochondriaPlasma CellsAMP-Activated Protein KinasesAntibodiesImmunoglobulinsPrkaa1 protein, mouseProtein Serine-Threonine Kinases

Identifiers

PMID33148712
PMCPMC7686102

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.