Evidence map›Paper›PMID 25760435›Full record

ArticleTissue engineering. Part A2015

Nonviral Reprogramming of Human Wharton's Jelly Cells Reveals Differences Between ATOH1 Homologues.

Adam J Mellott, Keerthana Devarajan, Heather E Shinogle, David S Moore, Zsolt Talata, Jennifer S Laurence, M Laird Forrest, Sumihare Noji, Eiji Tanaka, Hinrich Staecker and 1 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Tissue engineering. Part A, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.9field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

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  5. 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

11 authors at 3 institutions in 2 countries.

Adam J Mellott1Bioengineering Graduate Program, University of Kansas, Lawrence, Kansas.
Keerthana Devarajan2Department of Genetics, Stanford University, Stanford, California.
Heather E Shinogle3Microscopy and Analytical Imaging Lab, University of Kansas, Lawrence, Kansas.
David S Moore3Microscopy and Analytical Imaging Lab, University of Kansas, Lawrence, Kansas.
Zsolt Talata4Department of Mathematics, University of Kansas, Lawrence, Kansas.
Jennifer S Laurence1Bioengineering Graduate Program, University of Kansas, Lawrence, Kansas.
M Laird Forrest1Bioengineering Graduate Program, University of Kansas, Lawrence, Kansas.
Sumihare Noji6Department of Life Systems, Institute of Technology and Science, The University of Tokushima, Minami-Jyosanjima-cho, Tokushima, Japan.
Eiji Tanaka7Department of Orthodontics and Dentofacial Orthopedics, Institute of Health Biosciences, The University of Tokushima Graduate School, Kuramoto-cho, Tokushima, Japan.
Hinrich Staecker1Bioengineering Graduate Program, University of Kansas, Lawrence, Kansas.
Michael S Detamore1Bioengineering Graduate Program, University of Kansas, Lawrence, Kansas.
University of Kansas · USStanford University · USTokushima University · JP

Funding

Participant Recruitment and ManagementP30DC005803 · NIDCD · UNIVERSITY OF KANSAS LAWRENCE · PI RICE, MABEL L · 2002 to 2016
$5.8M
Biomaterials for treatment of head and neck cancerR01CA173292 · NCI · UNIVERSITY OF KANSAS LAWRENCE · PI FORREST, MARCUS LAIRD · 2013 to 2017
$1.4M
Gradient-based strategy for osteochondral regenerationR01AR056347 · NIAMS · UNIVERSITY OF KANSAS LAWRENCE · PI DETAMORE, MICHAEL S. · 2010 to 2014
$1.3M
NCI NIH HHS R01 CA173292NIAMS NIH HHS R01 AR056347NIDCD NIH HHS P30 DC005803
6 · The paper itself

Abstract

The transcription factor atonal homolog 1 (ATOH1) has multiple homologues that are functionally conserved across species and is responsible for the generation of sensory hair cells. To evaluate potential functional differences between homologues, human and mouse ATOH1 (HATH1 and MATH-1, respectively) were nonvirally delivered to human Wharton's jelly cells (hWJCs) for the first time. Delivery of HATH1 to hWJCs demonstrated superior expression of inner ear hair cell markers and characteristics than delivery of MATH-1. Inhibition of HES1 and HES5 signaling further increased the atonal effect. Transfection of hWJCs with HATH1 DNA, HES1 siRNA, and HES5 siRNA displayed positive identification of key hair cell and support cell markers found in the cochlea, as well as a variety of cell shapes, sizes, and features not native to hair cells, suggesting the need for further examination of other cell types induced by HATH1 expression. In the first side-by-side evaluation of HATH1 and MATH-1 in human cells, substantial differences were observed, suggesting that the two atonal homologues may not be interchangeable in human cells, and artificial expression of HATH1 in hWJCs requires further study. In the future, this line of research may lead to engineered systems that would allow for evaluation of drug ototoxicity or potentially even direct therapeutic use.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCell LineageCellular Reprogramming TechniquesFemaleFluorescent DyesGenetic VectorsHair Cells, Auditory, InnerHomeodomain ProteinsHumansInfant, NewbornMaleMesenchymal Stem CellsMiceMyosinsMyosin VIIaATOH1 protein, humanAtoh1 protein, mouseBasic Helix-Loop-Helix ProteinsFluorescent DyesFM1 43HES1 protein, humanHES5 protein, humanHomeodomain ProteinsMYO7A protein, humanMyo7a protein, mouseMyosinsMyosin VIIaPyridinium CompoundsQuaternary Ammonium CompoundsRepressor ProteinsRNA, Small InterferingTranscription Factor HES-1

Identifiers

PMID25760435
PMCPMC4449705
OpenAlexW1616161146

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.