Evidence map›Paper›PMID 22871841›Full record

ArticleInvestigative ophthalmology & visual science2012

Using flow cytometry to compare the dynamics of photoreceptor outer segment phagocytosis in iPS-derived RPE cells.

Peter D Westenskow, Stacey K Moreno, Tim U Krohne, Toshihide Kurihara, Saiyong Zhu, Zhen-Ning Zhang, Tongbiao Zhao, Yang Xu, Sheng Ding, Martin Friedlander

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
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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

10 authors at 3 institutions in 1 country.

Peter D WestenskowDepartment of Cell Biology, The Scripps Research Institute, La Jolla, California, USA.
Stacey K Moreno
Tim U Krohne
Toshihide Kurihara
Saiyong Zhu
Zhen-Ning Zhang
Tongbiao Zhao
Yang Xu
Sheng Ding
Martin Friedlander
Scripps Research Institute · USGladstone Institutes · USUniversity of California, San Francisco · US

Funding

INTEGRINS AND OCULAR ANGIOGENESISR01EY011254 · NEI · SCRIPPS RESEARCH INSTITUTE, THE · PI FRIEDLANDER, MARTIN · 1996 to 2016
$11.5M
Recapitulating developmental pathways to improve iPSC-RPE derivation protocolsF32EY021416 · NEI · SCRIPPS RESEARCH INSTITUTE, THE · PI WESTENSKOW, PETER DWAYNE · 2011 to 2013
$148k
NEI NIH HHS EY021416NEI NIH HHS EY11254NEI NIH HHS F32 EY021416NEI NIH HHS R01 EY011254
6 · The paper itself

Abstract

purposeRetinal pigment epithelium (RPE) autologous grafts can be readily derived from induced pluripotent stem (iPS) cells. It is critical to stringently characterize iPS-RPE using standardized and quantifiable methods to be confident that they are safe and adequate replacements for diseased RPE before utilizing them in clinical settings. One important and required function is that the iPS-RPE phagocytose photoreceptor outer segments (POS).

methodsWe developed a flow cytometry-based assay to monitor binding and internalization of FITC labeled POS by ARPE-19, human fetal RPE (hfRPE), and two types of iPS-RPE. Expression and density of α(v)β₅ integrin, CD36, and MerTK receptors, which are required for phagocytosis, were compared.

resultsTrypsinization of treated RPE cells results in the release of bound POS. The number of freed POS, the percentage of cells that internalized POS, the brightness of the FITC signal from the cells, and the surface density of the phagocytosis receptors on single RPE cells were measured using flow cytometry. These assays reveal that receptor density is dynamic during differentiation and this can affect the binding and internalization dynamics of the RPE cells. Highly differentiated iPS-RPE phagocytose POS more efficiently than hfRPE.

conclusionsCaution should be exercised to not use RPE grafts until demonstrating that they are fully functional. The density of the phagocytosis receptors is dynamic and may be used as a predictor for how well the iPS-RPE cells will function in vivo. The phagocytosis dynamics observed between iPS-RPE and primary RPE is very encouraging and adds to mounting evidence that iPS-RPE may be a viable replacement for dysfunctional or dying RPE in human patients.

Indexed as

AnimalsEye ProteinsFlow CytometryHumansInduced Pluripotent Stem CellsPhagocytosisReceptors, ImmunologicRetinal Photoreceptor Cell Outer SegmentSwineEye Proteinsphagocytosis receptorReceptors, Immunologic

Identifiers

PMID22871841
PMCPMC3444211
OpenAlexW1964936056

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.