Evidence map›Paper›PMID 22205632›Full record

ArticleAmerican journal of respiratory cell and molecular biology2012

LPS-stimulated cytokine production in type I cells is modulated by the renin-angiotensin system.

Mandi H Wong, Olivia C Chapin, Meshell D Johnson

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. International journal of chronic obstructive pulmonary disease · 2018
    Pooled it
  2. Trial
  3. Immunology of Sepsis.Clinics in chest medicine · 2026
    Review
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  18. Cell fate analysis in fetal mouse lung reveals distinct pathways for TI and TII cell development.American journal of physiology. Lung cellular and molecular physiology · 2019
    Article
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  20. 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

3 authors at 2 institutions in 1 country.

Mandi H WongSan Francisco VA Medical Center, 4150 Clement St., San Francisco, CA 94121, USA.
Olivia C Chapin
Meshell D Johnson
San Francisco VA Medical Center · USUniversity of California, San Francisco · US

Funding

Ion Transport in Alveolar Type I CellsK08HL088025 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JOHNSON, MESHELL · 2008 to 2009
$220k
NHLBI NIH HHS HL088025NHLBI NIH HHS K08 HL088025
6 · The paper itself

Abstract

The alveolar epithelium serves as a barrier to the entry of potential respiratory pathogens. Alveolar Type II (TII) cells have immunomodulatory functions, but whether Type I (TI) cells, which comprise approximately 95% of the alveolar epithelium, also play a role in immunity is unknown. Because the renin-angiotensin system (RAS) is emerging as an important mediator of inflammation, and angiotensin-converting enzyme 2 (ACE2), an element of the RAS, has been implicated in lung injury, we hypothesize that TI cells can produce cytokines in response to LPS stimulation, and that this inflammation can be modulated by the RAS. Alveolar TI cells were isolated from adult Sprague-Dawley rat lungs that had been injured with an intratracheal instillation of LPS. PCR was performed to determine whether TI cells expressed transcripts for TNF-α, IL-6, or IL-1β at baseline and after lung injury. Immunocytochemical and protein analysis detected angiotensin II (Ang II) and ACE2, as well as angiotensin Type 1 receptor (AT1R) and Type 2 receptor (AT2R), in TI cells. To separate cell-specific responses, primary TI cells were isolated, cultured, and exposed to LPS, Ang II, or specific inhibitors of AT1R or AT2R. Cytokine production was assayed by ELISA. LPS stimulated the production of all cytokines, whereas ACE2 and losartan, an AT1R inhibitor, blocked elements of the LPS-induced cytokine response. Primary TI cells produce cytokines when treated with LPS, contain important components of the RAS, and can modulate LPS-induced cytokine production via the RAS, suggesting a role for TI cells in the innate immune response of the lung.

Indexed as

AnimalsBlotting, WesternCytokinesEnzyme-Linked Immunosorbent AssayImmunohistochemistryLipopolysaccharidesMalePolymerase Chain ReactionRatsRats, Sprague-DawleyRenin-Angiotensin SystemRNA, MessengerToll-Like Receptor 4CytokinesLipopolysaccharidesRNA, MessengerToll-Like Receptor 4

Identifiers

PMID22205632
PMCPMC3359899
OpenAlexW2060256297

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.