Evidence map›Paper›PMID 24441790›Full record

ArticleNature immunology2014

Inducible nitric oxide synthase is a major intermediate in signaling pathways for the survival of plasma cells.

Ankur S Saini, Gautam N Shenoy, Satyajit Rath, Vineeta Bal, Anna George

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

38 citing papers in PubMed, 55 citations in OpenAlex.

  1. Trial
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  11. Arginine-dependent immune responses.Cellular and molecular life sciences : CMLS · 2021
    Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Macrophage, the potential key mediator in CAR-T related CRS.Experimental hematology & oncology · 2020
    Review
  17. Plasma cells: You are what you eat.Immunological reviews · 2019
    Review
  18. The Maintenance of Memory Plasma Cells.Frontiers in immunology · 2019
    Review
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Ankur S Saini1] National Institute of Immunology, New Delhi, India. [2].
Gautam N Shenoy1] National Institute of Immunology, New Delhi, India. [2] [3].
Satyajit Rath1] National Institute of Immunology, New Delhi, India. [2].
Vineeta Bal1] National Institute of Immunology, New Delhi, India. [2].
Anna George1] National Institute of Immunology, New Delhi, India. [2].
National Institute of Immunology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While a number of extrinsic factors are known to promote the survival of plasma cells (PCs), the signaling intermediates involved remain poorly characterized. Here we identified inducible nitric oxide synthase (iNOS) as an intermediate that supported the survival of PCs. PCs deficient in iNOS (Nos2(-/-) PCs) showed enhanced death in vitro, after transfer into congenic adoptive hosts, and in chimeras made with wild-type and Nos2(-/-) bone marrow. The iNOS-mediated protection involved activation of protein kinase G and modulation of endoplasmic reticulum stress components. Activation of caspases was also diminished. We found that iNOS was required for PCs to respond to some prosurvival mediators associated with bone marrow stromal cells and that at least one mediator, interleukin 6, fed directly into this pathway by inducing iNOS.

Indexed as

Adoptive TransferAnimalsCell SurvivalFlow CytometryMiceMice, Inbred C57BLMice, KnockoutNitric Oxide Synthase Type IIPlasma CellsReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionSignal TransductionNitric Oxide Synthase Type IINos2 protein, mouse

Identifiers

PMID24441790
OpenAlexW2005920676

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.