Evidence map›Paper›PMID 29722564›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2018

Long-term culture and cloning of primary human bronchial basal cells that maintain multipotent differentiation capacity and CFTR channel function.

Jennifer R Peters-Hall, Melissa L Coquelin, Michael J Torres, Ryan LaRanger, Busola R Alabi, Sei Sho, Jose F Calva-Moreno, Philip J Thomas, Jerry W Shay

Abstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Article
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  12. Conditionally reprogrammed asthmatic bronchial epithelial cells express lowerAmerican journal of physiology. Lung cellular and molecular physiology · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Stem Cell-derived Respiratory Epithelial Cell Cultures as Human Disease Models.American journal of respiratory cell and molecular biology · 2021
    Review
  18. Review
  19. Article
  20. Review
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

9 authors.

Jennifer R Peters-HallDepartment of Cell Biology, University of Texas Southwestern Medical Center , Dallas, Texas.
Melissa L CoquelinDepartment of Cell Biology, University of Texas Southwestern Medical Center , Dallas, Texas.
Michael J TorresDepartment of Physiology, University of Texas Southwestern Medical Center , Dallas, Texas.
Ryan LaRangerDepartment of Cell Biology, University of Texas Southwestern Medical Center , Dallas, Texas.
Busola R AlabiDepartment of Cell Biology, University of Texas Southwestern Medical Center , Dallas, Texas.
Sei ShoDepartment of Cell Biology, University of Texas Southwestern Medical Center , Dallas, Texas.
Jose F Calva-MorenoDepartment of Cell Biology, University of Texas Southwestern Medical Center , Dallas, Texas.
Philip J ThomasDepartment of Physiology, University of Texas Southwestern Medical Center , Dallas, Texas.
Jerry W ShayDepartment of Cell Biology, University of Texas Southwestern Medical Center , Dallas, Texas.

Funding

Cancer Biology Training GrantT32CA124334 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI SHAY, JERRY WILLIAM · 2007 to 2021
$5.3M
DEVELOPMENT OF MEMBRANE PROTEIN STRUCTURER37DK049835 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI THOMAS, PHILIP J · 2008 to 2017
$3.6M
In vivo multiphoton microscope for UT Southwestern Live Cell Imaging FacilityS10RR029731 · NCRR · UT SOUTHWESTERN MEDICAL CENTER · PI LUBY-PHELPS, KATHERINE J · 2010 to 2010
$1.2M
NCI NIH HHS T32 CA124334NCRR NIH HHS S10 RR029731NIDDK NIH HHS R37 DK049835
6 · The paper itself

Abstract

While primary cystic fibrosis (CF) and non-CF human bronchial epithelial basal cells (HBECs) accurately represent in vivo phenotypes, one barrier to their wider use has been a limited ability to clone and expand cells in sufficient numbers to produce rare genotypes using genome-editing tools. Recently, conditional reprogramming of cells (CRC) with a Rho-associated protein kinase (ROCK) inhibitor and culture on an irradiated fibroblast feeder layer resulted in extension of the life span of HBECs, but differentiation capacity and CF transmembrane conductance regulator (CFTR) function decreased as a function of passage. This report details modifications to the standard HBEC CRC protocol (Mod CRC), including the use of bronchial epithelial cell growth medium, instead of F medium, and 2% O

Indexed as

Cell Differentiation3T3 CellsAnimalsBronchiCell Culture TechniquesCells, CulturedCellular Reprogramming TechniquesCRISPR-Cas SystemsCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorGene EditingHumansMiceMultipotent Stem CellsTime FactorsCFTR protein, humanCystic Fibrosis Transmembrane Conductance Regulatorconditional reprogrammingCRISPRcystic fibrosishuman bronchial epithelial cellsROCK inhibitor

Identifiers

PMID29722564
PMCPMC6139663

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.