Evidence map›Paper›PMID 28811631›Full record

ArticleScientific reports2017

Development of a Primary Human Co-Culture Model of Inflamed Airway Mucosa.

Lael M Yonker, Hongmei Mou, Kengyeh K Chu, Michael A Pazos, Huimin Leung, Dongyao Cui, Jinhyeob Ryu, Rhianna M Hibbler, Alexander D Eaton, Tim N Ford and 5 more

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
–field-weighted citation impact
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

48 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
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  11. Macrophages and the microbiome in chronic obstructive pulmonary disease.European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
  12. Blocking HXAmBio · 2024
    Article
  13. Article
  14. Recreating chronic respiratory infectionsEuropean respiratory review : an official journal of the European Respiratory Society · 2024
    Review
  15. Blocking HXAbioRxiv : the preprint server for biology · 2024
    Article
  16. Review
  17. Modeling airway persistent infection ofFrontiers in cellular and infection microbiology · 2024
    Article
  18. On the path to predicting immune responses in the lung: Modeling the pulmonary innate immune system at the air-liquid interface (ALI).European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences · 2023
    Review
  19. Article
  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

15 authors.

Lael M YonkerDepartment of Pediatrics, Harvard Medical School, Boston, MA, USA.ORCID 0000-0003-1711-8227
Hongmei MouDepartment of Pediatrics, Harvard Medical School, Boston, MA, USA.
Kengyeh K ChuDepartment of Pathology, Harvard Medical School, Boston, MA, USA.
Michael A PazosDepartment of Pediatrics, Harvard Medical School, Boston, MA, USA.
Huimin LeungDepartment of Pathology, Harvard Medical School, Boston, MA, USA.
Dongyao CuiDepartment of Pathology, Harvard Medical School, Boston, MA, USA.
Jinhyeob RyuWellman Center for Photomedicine, Massachusetts General Hospital, Boston, MA, USA.
Rhianna M HibblerMucosal Immunology and Biology Research Center, Massachusetts General Hospital, Boston, MA, USA.
Alexander D EatonMucosal Immunology and Biology Research Center, Massachusetts General Hospital, Boston, MA, USA.
Tim N FordDepartment of Pathology, Harvard Medical School, Boston, MA, USA.
J R FalckDepartments of Biochemistry and Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
T Bernard KinaneDepartment of Pediatrics, Harvard Medical School, Boston, MA, USA.
Guillermo J TearneyDepartment of Pathology, Harvard Medical School, Boston, MA, USA.
Jayaraj RajagopalDepartment of Medicine, Harvard Medical School, Boston, MA, USA.
Bryan P HurleyDepartment of Pediatrics, Harvard Medical School, Boston, MA, USA. bphurley@mgh.harvard.edu.

Funding

The Role of Hepoxilin A3 in Neutrophil Breach of the Infected Airway MucosaR01AI095338 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI HURLEY, BRYAN P · 2012 to 2022
$5.2M
Intercellular communication and cell regulation in airway epithelial ensembles in regeneration and diseaseR01HL118185 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI RAJAGOPAL, JAYARAJ · 2014 to 2021
$4.2M
Defining the role of Hippo signaling in airway injury repair and remodelingR01HL116756 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI RAJAGOPAL, JAYARAJ · 2013 to 2017
$2.2M
NHLBI NIH HHS R01 HL116756NHLBI NIH HHS R01 HL118185NIAID NIH HHS R01 AI095338
6 · The paper itself

Abstract

Neutrophil breach of the mucosal surface is a common pathological consequence of infection. We present an advanced co-culture model to explore neutrophil transepithelial migration utilizing airway mucosal barriers differentiated from primary human airway basal cells and examined by advanced imaging. Human airway basal cells were differentiated and cultured at air-liquid interface (ALI) on the underside of 3 µm pore-sized transwells, compatible with the study of transmigrating neutrophils. Inverted ALIs exhibit beating cilia and mucus production, consistent with conventional ALIs, as visualized by micro-optical coherence tomography (µOCT). µOCT is a recently developed imaging modality with the capacity for real time two- and three-dimensional analysis of cellular events in marked detail, including neutrophil transmigratory dynamics. Further, the newly devised and imaged primary co-culture model recapitulates key molecular mechanisms that underlie bacteria-induced neutrophil transepithelial migration previously characterized using cell line-based models. Neutrophils respond to imposed chemotactic gradients, and migrate in response to Pseudomonas aeruginosa infection of primary ALI barriers through a hepoxilin A3-directed mechanism. This primary cell-based co-culture system combined with µOCT imaging offers significant opportunity to probe, in great detail, micro-anatomical and mechanistic features of bacteria-induced neutrophil transepithelial migration and other important immunological and physiological processes at the mucosal surface.

Indexed as

Cell Culture TechniquesCoculture Techniques8,11,14-Eicosatrienoic AcidCell LineCell MovementCell PolarityChemotaxis, LeukocyteEpithelial CellsFluorescent Antibody TechniqueHumansInflammationNeutrophil InfiltrationNeutrophilsRespiratory Mucosa8,11,14-Eicosatrienoic Acid8-hydroxy-11,12-epoxyeicosa-5,9,14-trienoic acid

Identifiers

PMID28811631
PMCPMC5557980

What OpenQuestion holds

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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.