Evidence map›Paper›PMID 19684200›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2009

Characteristics of Cl- uptake in rat alveolar type I cells.

Meshell Johnson, Lennell Allen, Leland Dobbs

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. CFTR as a therapeutic target for severe lung infection.American journal of physiology. Lung cellular and molecular physiology · 2025
    Review
  3. Ion channels of the lung and their role in disease pathogenesis.American journal of physiology. Lung cellular and molecular physiology · 2017
    Review
  4. The role of stretch-activated ion channels in acute respiratory distress syndrome: finally a new target?American journal of physiology. Lung cellular and molecular physiology · 2016
    Review
  5. Article
  6. Article
  7. CFTR is required for maximal transepithelial liquid transport in pig alveolar epithelia.American journal of physiology. Lung cellular and molecular physiology · 2012
    Article
  8. Ion transport by pulmonary epithelia.Journal of biomedicine & biotechnology · 2011
    Review
  9. Article
  10. Mitigation of chlorine lung injury by increasing cyclic AMP levels.Proceedings of the American Thoracic Society · 2010
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 2 countries.

Meshell JohnsonDepartment of Medicine, University of California, San Francisco, 3333 California St., Suite 150, Box 1245, San Francisco, CA 94118, USA. meshell.johnson@ucsf.edu
Lennell Allen
Leland Dobbs
Cardiovascular Institute Hospital · JPSan Francisco VA Medical Center · USUniversity of California, San Francisco · US

Funding

TENASCINS AND LUNG INJURYP01HL024075 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GILLESPIE, ANNE-MARIE · 1985 to 2015
$25.8M
PLASTICITY OF ALVEOLAR EPITHELIAL PHENOTYPIC EXPRESSIONR01HL057426 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DOBBS, LELAND GEORGE · 1997 to 2008
$3.0M
Ion Transport in Alveolar Type I CellsK08HL088025 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JOHNSON, MESHELL · 2008 to 2009
$220k
NHLBI NIH HHS HL-088025NHLBI NIH HHS HL-24075NHLBI NIH HHS HL-57426
6 · The paper itself

Abstract

Although Cl- transport in fetal lung is important for fluid secretion and normal lung development, the role of Cl- transport in adult lung is not well understood. In physiological studies, the cystic fibrosis transmembrane regulator (CFTR) plays a role in fluid absorption in the distal air spaces of adult lung, and alveolar type II cells cultured for 5 days have the capacity to transport Cl-. Although both alveolar type I and type II cells express CFTR, it has previously not been known whether type I cells transport Cl-. We studied Cl- uptake in isolated type I cells directly, using either radioisotopic tracers or halide-sensitive fluorescent indicators. By both methods, type I cells take up Cl-. In the presence of beta-adrenergic agonist stimulation, Cl- uptake can be inhibited by CFTR antagonists. Type I cells express both the Cl-/HCO3- anion exchanger AE2 and the voltage-gated Cl- channels CLC5 and CLC2. Inhibitors of AE2 also block Cl- uptake in type I cells. Together, these results demonstrate that type I cells are capable of Cl- uptake and suggest that the effects seen in whole lung studies establishing the importance of Cl- movement in alveolar fluid clearance may be, in part, the result of Cl- transport across type I cells.

Indexed as

4,4'-Diisothiocyanostilbene-2,2'-Disulfonic AcidAdrenergic beta-AgonistsAmilorideAnimalsAnion Transport ProteinsAntiportersBumetanideChloridesCystic Fibrosis Transmembrane Conductance RegulatorEpithelial CellsFluorescenceGene Expression RegulationImmunohistochemistryNitrobenzoatesPulmonary AlveoliQuinolinium Compounds4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid5-nitro-2-(3-phenylpropylamino)benzoic acidAdrenergic beta-AgonistsAmilorideAnion Transport ProteinsAntiportersBumetanideChloridesCystic Fibrosis Transmembrane Conductance RegulatorN-(ethoxycarbonylmethyl)-6-methoxyquinoliniumNitrobenzoatesQuinolinium CompoundsRadioisotopesRNA, MessengerSLC4A ProteinsTerbutaline

Identifiers

PMID19684200
PMCPMC2777494
OpenAlexW2159317627

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.