Evidence map›Paper›PMID 33570622›Full record

ArticleBlood advances2021

Polarized mitochondria as guardians of NK cell fitness.

Laura Surace, Jean-Marc Doisne, Pedro Escoll, Solenne Marie, Valerie Dardalhon, Carys Croft, Anna Thaller, Davide Topazio, Angelo Sparaneo, Antonia Cama and 5 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 56 citations in OpenAlex.

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  15. Nutrient transporter pattern in CD56Frontiers in immunology · 2024
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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

15 authors at 5 institutions in 2 countries.

Laura SuraceINSERM U1223, Paris, France.
Jean-Marc DoisneINSERM U1223, Paris, France.
Pedro EscollBiology of Intracellular Bacteria Unit, Institut Pasteur, Paris, France.
Solenne MarieINSERM U1223, Paris, France.
Valerie DardalhonInstitut de Génétique Moléculaire de Montpellier, University of Montpellier, CNRS, Montpellier, France.
Carys CroftINSERM U1223, Paris, France.
Anna ThallerINSERM U1223, Paris, France.
Davide TopazioHead and Neck Department, "Casa Sollievo della Sofferenza," Scientific Institute for Research and Health Care (IRCCS), San Giovanni Rotondo, Italy.
Angelo SparaneoLaboratory of Oncology, "Casa Sollievo della Sofferenza," IRCCS, San Giovanni Rotondo, Italy.
Antonia CamaMaxillofacial Surgery Unit, Department of Neuroscience, University Federico II, Naples, Italy; and.
Olimpia MusumeciUnit of Neurology and Neuromuscular Disorders, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Aurelio d'EcclesiaHead and Neck Department, "Casa Sollievo della Sofferenza," Scientific Institute for Research and Health Care (IRCCS), San Giovanni Rotondo, Italy.
Carmen BuchrieserBiology of Intracellular Bacteria Unit, Institut Pasteur, Paris, France.
Naomi TaylorInstitut de Génétique Moléculaire de Montpellier, University of Montpellier, CNRS, Montpellier, France.
James P Di SantoINSERM U1223, Paris, France.
Inserm · FRCentre National de la Recherche Scientifique · FRCasa Sollievo della Sofferenza · ITFederico II University Hospital · ITUniversity of Messina · IT

Funding

Metabolic regulation of T cell effector function and anti-tumor immunotherapyZIABC011923 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TAYLOR, NAOMI · 2019 to 2025
$9.5M
Reprogramming hematopoietic stem cell (HSC) differentiation via metabolic conditZIABC011924 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TAYLOR, NAOMI · 2019 to 2025
$9.0M
6 · The paper itself

Abstract

Distinct metabolic demands accompany lymphocyte differentiation into short-lived effector and long-lived memory cells. How bioenergetics processes are structured in innate natural killer (NK) cells remains unclear. We demonstrate that circulating human CD56Dim (NKDim) cells have fused mitochondria and enhanced metabolism compared with CD56Br (NKBr) cells. Upon activation, these 2 subsets showed a dichotomous response, with further mitochondrial potentiation in NKBr cells vs paradoxical mitochondrial fission and depolarization in NKDim cells. The latter effect impaired interferon-γ production, but rescue was possible by inhibiting mitochondrial fragmentation, implicating mitochondrial polarization as a central regulator of NK cell function. NKDim cells are heterogeneous, and mitochondrial polarization was associated with enhanced survival and function in mature NKDim cells, including memory-like human cytomegalovirus-dependent CD57+NKG2C+ subsets. In contrast, patients with genetic defects in mitochondrial fusion had a deficiency in adaptive NK cells, which had poor survival in culture. These results support mitochondrial polarization as a central regulator of mature NK cell fitness.

Indexed as

Cytomegalovirus InfectionsCytomegalovirusHumansKiller Cells, NaturalLymphocyte ActivationMitochondria

Identifiers

PMID33570622
PMCPMC7805327
OpenAlexW3114717232

What OpenQuestion holds

Textmetadata
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.