Evidence map›Paper›PMID 30323255›Full record

ArticleNature communications2018

Mrp1 is involved in lipid presentation and iNKT cell activation by Streptococcus pneumoniae.

Shilpi Chandra, James Gray, William B Kiosses, Archana Khurana, Kaori Hitomi, Catherine M Crosby, Ashu Chawla, Zheng Fu, Meng Zhao, Natacha Veerapen and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. The iNKT Cell-Macrophage Axis in Homeostasis and Disease.International journal of molecular sciences · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. ABCC3 Expressed by CD56International journal of molecular sciences · 2019
    Article
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

17 authors at 4 institutions in 2 countries.

Shilpi ChandraDivision of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA.
James GrayThe Functional Genomics Center, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA.
William B KiossesDivision of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA.
Archana KhuranaDivision of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA.
Kaori HitomiDivision of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA.
Catherine M CrosbyDivision of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA.
Ashu ChawlaBioinformatics Core, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA.
Zheng FuBioinformatics Core, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA.ORCID http://orcid.org/0000-0002-0281-3043
Meng ZhaoDivision of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA.
Natacha VeerapenSchool of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
Stewart K RichardsonDepartment of Chemistry, University of Connecticut, 55N. Eagleville Rd, Storrs, CT, 06269, USA.
Steven A PorcelliDepartment of Microbiology and Immunology, and Department of Medicine, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY, 10461, USA.
Gurdyal BesraSchool of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.ORCID http://orcid.org/0000-0002-5605-0395
Amy R HowellDepartment of Chemistry, University of Connecticut, 55N. Eagleville Rd, Storrs, CT, 06269, USA.
Sonia SharmaThe Functional Genomics Center, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA.
Bjoern PetersDivision of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA.
Mitchell KronenbergDivision of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA. mitch@lji.org.ORCID http://orcid.org/0000-0001-6318-6445
La Jolla Institute for Immunology · USUniversity of Birmingham · GBUniversity of Connecticut · USAlbert Einstein College of Medicine · US

Funding

New players in immune function: identification through RNAi and micro-RNA screensRC4AI092763 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI KRONENBERG, MITCHELL, RAO, ANJANA · 2010 to 2010
$12.6M
Precision Targeting of CD1-Restricted iNKT Cells for Cancer ImmunotherapyR01AI045889 · NIAID · YESHIVA UNIVERSITY · PI Steven A Porcelli · 1999 to 2026
$9.3M
Development and Function of NKT CellsR37AI071922 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI KRONENBERG, MITCHELL · 2006 to 2015
$4.9M
Rheumatic Diseases Research Training GrantT32AR064194 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GARY S FIRESTEIN, Monica Guma · 2013 to 2026
$3.8M
Recognition of bacterial antigens by NKT cellsR01AI045053 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI KRONENBERG, MITCHELL · 2000 to 2010
$3.3M
Differentiation of subsets of NKT cellsR01AI071922 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI KRONENBERG, MITCHELL · 2016 to 2020
$2.7M
The role of natural killer T cells in the innate response to lung infectionR01AI105215 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI KRONENBERG, MITCHELL · 2014 to 2018
$2.2M
Harnessing NKT Cell Activation by GlycolipidsR01GM111849 · NIGMS · UNIVERSITY OF CONNECTICUT STORRS · PI HOWELL, AMY · 2019 to 2022
$2.1M
Targeting tumor endothelium for cancer surveillance and immunotherapyR01CA199376 · NCI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI SHARMA, SONIA · 2015 to 2019
$2.0M
Harnessing NKT Cell Activation by GlycolipidsU01GM111849 · NIGMS · UNIVERSITY OF CONNECTICUT STORRS · PI HOWELL, AMY · 2014 to 2017
$1.9M
FACSAria II Cell SorterS10RR027366 · NCRR · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROFT, MICHAEL · 2011 to 2011
$514k
NCI NIH HHS R01 CA199376NCRR NIH HHS S10 RR027366NIAID NIH HHS R01 AI045053NIAID NIH HHS R01 AI045889NIAID NIH HHS R01 AI071922NIAID NIH HHS R01 AI105215NIAID NIH HHS R37 AI071922NIAID NIH HHS RC4 AI092763NIAMS NIH HHS T32 AR064194NIGMS NIH HHS R01 GM111849NIGMS NIH HHS U01 GM111849U.S. Department of Health & Human Services | National Institutes of Health (NIH) AI092763-01U.S. Department of Health & Human Services | National Institutes of Health (NIH) AI45053U.S. Department of Health & Human Services | National Institutes of Health (NIH) AI45889U.S. Department of Health & Human Services | National Institutes of Health (NIH) AI71922U.S. Department of Health & Human Services | National Institutes of Health (NIH) GM111849U.S. Department of Health & Human Services | National Institutes of Health (NIH) S10RR027366
6 · The paper itself

Abstract

Invariant natural killer T cells (iNKT cells) are activated by lipid antigens presented by CD1d, but the pathway leading to lipid antigen presentation remains incompletely characterized. Here we show a whole-genome siRNA screen to elucidate the CD1d presentation pathway. A majority of gene knockdowns that diminish antigen presentation reduced formation of glycolipid-CD1d complexes on the cell surface, including members of the HOPS and ESCRT complexes, genes affecting cytoskeletal rearrangement, and ABC family transporters. We validated the role in vivo for the multidrug resistance protein 1 (Mrp1) in CD1d antigen presentation. Mrp1 deficiency reduces surface clustering of CD1d, which decreased iNKT cell activation. Infected Mrp1 knockout mice show decreased iNKT cell responses to antigens from Streptococcus pneumoniae and were associated with increased mortality. Our results highlight the unique cellular events involved in lipid antigen presentation and show how modification of this pathway can lead to lethal infection.

Indexed as

AnimalsAntigen PresentationAntigens, CD1dATP Binding Cassette Transporter, Subfamily B, Member 1Cell LineEndosomesGene Regulatory NetworksLipidsLymphocyte ActivationLysosomesMacrophagesMembrane MicrodomainsMice, Inbred BALB CMice, KnockoutNatural Killer T-CellsRNA, Small InterferingAntigens, CD1dATP Binding Cassette Transporter, Subfamily B, Member 1LipidsRNA, Small Interfering

Identifiers

PMID30323255
PMCPMC6189046
OpenAlexW2896532486

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.