Evidence map›Paper›PMID 28483697›Full record

ArticleActa biomaterialia2017

Preparation and evaluation of human choroid extracellular matrix scaffolds for the study of cell replacement strategies.

Kathleen R Chirco, Kristan S Worthington, Miles J Flamme-Wiese, Megan J Riker, Joshua D Andrade, Beatrix M Ueberheide, Edwin M Stone, Budd A Tucker, Robert F Mullins

Abstract read
In one paragraph

Article in Acta biomaterialia, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

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  12. USP7 Cooperates with NOTCH1 to Drive the Oncogenic Transcriptional Program in T-Cell Leukemia.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
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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 at 2 institutions in 1 country.

Kathleen R ChircoThe Stephen A. Wynn Institute for Vision Research, The University of Iowa, Iowa City, IA 52246, USA; Department of Ophthalmology and Visual Sciences, The University of Iowa, Iowa City, IA 52246, USA.
Kristan S WorthingtonThe Stephen A. Wynn Institute for Vision Research, The University of Iowa, Iowa City, IA 52246, USA; Department of Ophthalmology and Visual Sciences, The University of Iowa, Iowa City, IA 52246, USA.
Miles J Flamme-WieseThe Stephen A. Wynn Institute for Vision Research, The University of Iowa, Iowa City, IA 52246, USA; Department of Ophthalmology and Visual Sciences, The University of Iowa, Iowa City, IA 52246, USA.
Megan J RikerThe Stephen A. Wynn Institute for Vision Research, The University of Iowa, Iowa City, IA 52246, USA; Department of Ophthalmology and Visual Sciences, The University of Iowa, Iowa City, IA 52246, USA.
Joshua D AndradeProteomics Laboratory, New York University School of Medicine, New York, NY 10016, USA.
Beatrix M UeberheideProteomics Laboratory, New York University School of Medicine, New York, NY 10016, USA; Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY 10016, USA.
Edwin M StoneThe Stephen A. Wynn Institute for Vision Research, The University of Iowa, Iowa City, IA 52246, USA; Department of Ophthalmology and Visual Sciences, The University of Iowa, Iowa City, IA 52246, USA.
Budd A TuckerThe Stephen A. Wynn Institute for Vision Research, The University of Iowa, Iowa City, IA 52246, USA; Department of Ophthalmology and Visual Sciences, The University of Iowa, Iowa City, IA 52246, USA.
Robert F MullinsThe Stephen A. Wynn Institute for Vision Research, The University of Iowa, Iowa City, IA 52246, USA; Department of Ophthalmology and Visual Sciences, The University of Iowa, Iowa City, IA 52246, USA. Electronic address: Robert-Mullins@uiowa.edu.
University of Iowa · USNew York University · US

Funding

Stem Cell and Organoid CoreP30EY025580 · NEI · UNIVERSITY OF IOWA · PI Michael G Anderson, Robert Foster Mullins · 2016 to 2026
$6.9M
Choriocapillaris Protection and Replacement in AMDR01EY024605 · NEI · UNIVERSITY OF IOWA · PI Robert Foster Mullins, Budd A Tucker · 2014 to 2026
$4.6M
NEI NIH HHS P30 EY025580NEI NIH HHS R01 EY024605
6 · The paper itself

Abstract

Endothelial cells (ECs) of the choriocapillaris are one of the first cell types lost during age-related macular degeneration (AMD), and cell replacement therapy is currently a very promising option for patients with advanced AMD. We sought to develop a reliable method for the production of human choroidal extracellular matrix (ECM) scaffolds, which will allow for the study of choroidal EC (CEC) replacement strategies in an environment that closely resembles the native tissue. Human RPE/choroid tissue was treated sequentially with Triton X-100, SDS, and DNase to remove all native cells. While all cells were successfully removed from the tissue, collagen IV, elastin, and laminin remained, with preserved architecture of the acellular vascular tubes. The ECM scaffolds were then co-cultured with exogenous ECs to determine if the tissue can support cell growth and allow EC reintegration into the decellularized choroidal vasculature. Both monkey and human ECs took up residence in the choriocapillary tubes of the decellularized tissue. Together, these data suggest that our decellularization methods are sufficient to remove all cellular material yet gentle enough to preserve tissue structure and allow for the optimization of cell replacement strategies. STATEMENT OF SIGNIFICANCE: Age-related macular degeneration (AMD) is a devastating disease affecting more than 600 million people worldwide. Endothelial cells of the choriocapillaris (CECs) are among the first cell types lost in early AMD, and cell replacement therapy is currently the most promising option for restoring vision in patients with advanced AMD. In order to study CEC replacement strategies we have generated a 3D choroid scaffold using a novel decellularization method in human RPE/choroid tissue. To our knowledge, this is the first report describing decellularization of human RPE/choroid, as well as recellularization of a choroid scaffold with CECs. This work will aid in our development and optimization of cell replacement strategies using a tissue scaffold that is similar to the in vivo environment.

Indexed as

AgedAged, 80 and overChoroidExtracellular MatrixExtracellular Matrix ProteinsFemaleHumansMacular DegenerationMaleTissue ScaffoldsExtracellular Matrix ProteinsAge-related macular degenerationChoriocapillarisChoroidDecellularizationExtracellular matrix

Identifiers

PMID28483697
PMCPMC5515248
OpenAlexW2611617945

What OpenQuestion holds

Textmetadata
LicenceTDM
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.