Evidence map›Paper›PMID 27022951›Full record

ArticleJournal of visualized experiments : JoVE2016

Cultivate Primary Nasal Epithelial Cells from Children and Reprogram into Induced Pluripotent Stem Cells.

Ashley Ulm, Christopher N Mayhew, Jason Debley, Gurjit K Khurana Hershey, Hong Ji

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Ashley UlmPyrosequencing Core, Cincinnati Children's Hospital.
Christopher N MayhewDivision of Developmental Biology, Cincinnati Children's Hospital.
Jason DebleyDivision of Pulmonary Medicine, Seattle Children's Hospital.
Gurjit K Khurana HersheyDivision of Asthma Research, Cincinnati Children's Hospital.
Hong JiPyrosequencing Core, Cincinnati Children's Hospital; Division of Asthma Research, Cincinnati Children's Hospital; Hong.Ji@cchmc.org.

Funding

LCenter for Clinical and Translational Science and TrainingUL1TR001425 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E., KISSELA, BRETT M · 2015 to 2024
$37.5M
TSLP, IL-9-producing mucosal mast cells, and allergic inflammationU19AI070235 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI Gurjit K. Khurana Hershey · 2006 to 2026
$31.3M
The role of CARDS toxin in genesis and exacerbation of allergic inflammationU19AI070412 · NIAID · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI BASEMAN, JOEL BARRY · 2006 to 2015
$19.7M
Cincinnati Center for Clinical and Translational Sciences and TrainingUL1TR000077 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E., TSEVAT, JOEL · 2012 to 2014
$9.9M
Dysregulated Airway Epithelial Signaling as a Driver of Airway Remodeling in Asthmatic ChildrenR01HL128361 · NHLBI · SEATTLE CHILDREN'S HOSPITAL · PI DEBLEY, JASON S · 2016 to 2018
$1.4M
The role of TET1 in childhood asthmaR21AI119236 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI JI, HONG · 2015 to 2016
$429k
DNA methylation in children hospitalized with asthma exacerbationR21AI101375 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI JI, HONG · 2012 to 2013
$409k
NCATS NIH HHS 8UL1TR000077-04NCATS NIH HHS UL1 TR000077NCATS NIH HHS UL1 TR001425NHLBI NIH HHS R01 HL128361NIAID NIH HHS 2U19AI70235NIAID NIH HHS R21 AI101375NIAID NIH HHS R21AI101375NIAID NIH HHS R21 AI119236NIAID NIH HHS R21AI119236NIAID NIH HHS U19 AI070235NIAID NIH HHS U19 AI070412
6 · The paper itself

Abstract

Nasal epithelial cells (NECs) are the part of the airways that respond to air pollutants and are the first cells infected with respiratory viruses. They are also involved in many airway diseases through their innate immune response and interaction with immune and airway stromal cells. NECs are of particular interest for studies in children due to their accessibility during clinical visits. Human induced pluripotent stem cells (iPSCs) have been generated from multiple cell types and are a powerful tool for modeling human development and disease, as well as for their potential applications in regenerative medicine. This is the first protocol to lay out methods for successful generation of iPSCs from NECs derived from pediatric participants for research purposes. It describes how to obtain nasal epithelial cells from children, how to generate primary NEC cultures from these samples, and how to reprogram primary NECs into well-characterized iPSCs. Nasal mucosa samples are useful in epidemiological studies related to the effects of air pollution in children, and provide an important tool for studying airway disease. Primary nasal cells and iPSCs derived from them can be a tool for providing unlimited material for patient-specific research in diverse areas of airway epithelial biology, including asthma and COPD research.

Indexed as

Cellular ReprogrammingChildEpithelial CellsHumansInduced Pluripotent Stem CellsNasal MucosaPrimary Cell Culture

Identifiers

PMID27022951
PMCPMC4792220

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.