Evidence map›Paper›PMID 22680980›Full record

ArticleMolecular pharmaceutics2012

Activation of the inflammasome and enhanced migration of microparticle-stimulated dendritic cells to the draining lymph node.

Ismail M Meraz, Brenda Melendez, Jianhua Gu, Stephen T C Wong, Xuewu Liu, Helen A Andersson, Rita E Serda

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 2012. 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
2.0field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 47 citations in OpenAlex.

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  11. Mitochondria-Targeted Nanomedicine for Enhanced Efficacy of Cancer Therapy.Frontiers in bioengineering and biotechnology · 2021
    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

7 authors at 1 institution in 1 country.

Ismail M MerazDepartment of Nanomedicine and §Department of Systems Medicine and Bioengineering, The Methodist Hospital Research Institute , 6670 Bertner Avenue, Houston, Texas 77030, United States.
Brenda Melendez
Jianhua Gu
Stephen T C Wong
Xuewu Liu
Helen A Andersson
Rita E Serda
Houston Methodist · US

Funding

The Core of the Computational BiologyU54CA149196 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WONG, STEPHEN TC · 2010 to 2015
$10.6M
Defining lineage-specific determinants of K-Ras "addiction" in human cancersR00CA149169 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SINGH, ANURAG · 2012 to 2014
$710k
Defining lineage-specific determinants of K-Ras "addiction" in human cancersK99CA149169 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI SINGH, ANURAG · 2010 to 2011
$268k
NCI NIH HHS K99 CA149169NCI NIH HHS R00 CA149169NCI NIH HHS U54CA149169NCI NIH HHS U54 CA149196
6 · The paper itself

Abstract

Porous silicon microparticles presenting pathogen-associated molecular patterns mimic pathogens, enhancing internalization of the microparticles and activation of antigen presenting dendritic cells. We demonstrate abundant uptake of microparticles bound by the TLR-4 ligands LPS and MPL by murine bone marrow-derived dendritic cells (BMDC). Labeled microparticles induce concentration-dependent production of IL-1β, with inhibition by the caspase inhibitor Z-VAD-FMK supporting activation of the NLRP3-dependent inflammasome. Inoculation of BALB/c mice with ligand-bound microparticles induces a significant increase in circulating levels of IL-1β, TNF-α, and IL-6. Stimulation of BMDC with ligand-bound microparticles increases surface expression of costimulatory and MHC molecules, and enhances migration of BMDC to the draining lymph node. LPS-microparticles stimulate in vivo C57BL/6 BMDC and OT-1 transgenic T cell interactions in the presence of OVA SIINFEKL peptide in lymph nodes, with intact nodes imaged using two-photon microscopy. Formation of in vivo and in vitro immunological synapses between BMDC, loaded with OVA peptide and LPS-microparticles, and OT-1 T cells are presented, as well as elevated intracellular interferon gamma levels in CD8(+) T cells stimulated by BMDC carrying peptide-loaded microparticles. In short, ligand-bound microparticles enhance (1) phagocytosis of microparticles; (2) BMDC inflammasome activation and upregulation of costimulatory and MHC molecules; (3) cellular migration of BMDC to lymphatic tissue; and (4) cellular interactions leading to T cell activation in the presence of antigen.

Indexed as

AnimalsBone Marrow CellsCD8-Positive T-LymphocytesCell MovementCells, CulturedDendritic CellsInflammasomesInterferon-gammaInterleukin-1betaInterleukin-6LigandsLipopolysaccharidesLymph NodesLymphocyte ActivationMiceMice, Inbred BALB CInflammasomesInterferon-gammaInterleukin-1betaInterleukin-6LigandsLipopolysaccharidesTumor Necrosis Factor-alpha

Identifiers

PMID22680980
PMCPMC3524399
OpenAlexW2044346213

What OpenQuestion holds

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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.