New Retinal Pigment Epithelial Cell Model to Unravel Neuroprotection Sensors of Neurodegeneration in Retinal Disease

Retinal pigment epithelial (RPE) cells sustain photoreceptor integrity, and when this function is disrupted, retinal degenerations ensue. Herein, we characterize a new cell line from human RPE that we termed ABC. These cells remarkably recapitulate human eye native cells. Distinctive from other epit...

Full description

Bibliographic Details
Main Authors: Aram Asatryan, Jorgelina M. Calandria, Marie-Audrey I. Kautzmann, Bokkyoo Jun, William C. Gordon, Khanh V. Do, Surjyadipta Bhattacharjee, Thang L. Pham, Vicente Bermúdez, Melina Valeria Mateos, Jessica Heap, Nicolas G. Bazan
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-06-01
Series:Frontiers in Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnins.2022.926629/full
_version_ 1818466285368901632
author Aram Asatryan
Jorgelina M. Calandria
Marie-Audrey I. Kautzmann
Bokkyoo Jun
William C. Gordon
Khanh V. Do
Surjyadipta Bhattacharjee
Thang L. Pham
Vicente Bermúdez
Melina Valeria Mateos
Jessica Heap
Nicolas G. Bazan
author_facet Aram Asatryan
Jorgelina M. Calandria
Marie-Audrey I. Kautzmann
Bokkyoo Jun
William C. Gordon
Khanh V. Do
Surjyadipta Bhattacharjee
Thang L. Pham
Vicente Bermúdez
Melina Valeria Mateos
Jessica Heap
Nicolas G. Bazan
author_sort Aram Asatryan
collection DOAJ
description Retinal pigment epithelial (RPE) cells sustain photoreceptor integrity, and when this function is disrupted, retinal degenerations ensue. Herein, we characterize a new cell line from human RPE that we termed ABC. These cells remarkably recapitulate human eye native cells. Distinctive from other epithelia, RPE cells originate from the neural crest and follow a neural development but are terminally differentiated into “epithelial” type, thus sharing characteristics with their neuronal lineages counterparts. Additionally, they form microvilli, tight junctions, and honeycomb packing and express distinctive markers. In these cells, outer segment phagocytosis, phagolysosome fate, phospholipid metabolism, and lipid mediator release can be studied. ABC cells display higher resistance to oxidative stress and are protected from senescence through mTOR inhibition, making them more stable in culture. The cells are responsive to Neuroprotectin D1 (NPD1), which downregulates inflammasomes and upregulates antioxidant and anti-inflammatory genes. ABC gene expression profile displays close proximity to native RPE lineage, making them a reliable cell system to unravel signaling in uncompensated oxidative stress (UOS) and retinal degenerative disease to define neuroprotection sites.
first_indexed 2024-04-13T20:56:43Z
format Article
id doaj.art-dc801f6830e94c9da53e42e67e678744
institution Directory Open Access Journal
issn 1662-453X
language English
last_indexed 2024-04-13T20:56:43Z
publishDate 2022-06-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Neuroscience
spelling doaj.art-dc801f6830e94c9da53e42e67e6787442022-12-22T02:30:19ZengFrontiers Media S.A.Frontiers in Neuroscience1662-453X2022-06-011610.3389/fnins.2022.926629926629New Retinal Pigment Epithelial Cell Model to Unravel Neuroprotection Sensors of Neurodegeneration in Retinal DiseaseAram AsatryanJorgelina M. CalandriaMarie-Audrey I. KautzmannBokkyoo JunWilliam C. GordonKhanh V. DoSurjyadipta BhattacharjeeThang L. PhamVicente BermúdezMelina Valeria MateosJessica HeapNicolas G. BazanRetinal pigment epithelial (RPE) cells sustain photoreceptor integrity, and when this function is disrupted, retinal degenerations ensue. Herein, we characterize a new cell line from human RPE that we termed ABC. These cells remarkably recapitulate human eye native cells. Distinctive from other epithelia, RPE cells originate from the neural crest and follow a neural development but are terminally differentiated into “epithelial” type, thus sharing characteristics with their neuronal lineages counterparts. Additionally, they form microvilli, tight junctions, and honeycomb packing and express distinctive markers. In these cells, outer segment phagocytosis, phagolysosome fate, phospholipid metabolism, and lipid mediator release can be studied. ABC cells display higher resistance to oxidative stress and are protected from senescence through mTOR inhibition, making them more stable in culture. The cells are responsive to Neuroprotectin D1 (NPD1), which downregulates inflammasomes and upregulates antioxidant and anti-inflammatory genes. ABC gene expression profile displays close proximity to native RPE lineage, making them a reliable cell system to unravel signaling in uncompensated oxidative stress (UOS) and retinal degenerative disease to define neuroprotection sites.https://www.frontiersin.org/articles/10.3389/fnins.2022.926629/fullneuroprotectin D1RPE cellsingle cellgene expressionlipidsapoptosis
spellingShingle Aram Asatryan
Jorgelina M. Calandria
Marie-Audrey I. Kautzmann
Bokkyoo Jun
William C. Gordon
Khanh V. Do
Surjyadipta Bhattacharjee
Thang L. Pham
Vicente Bermúdez
Melina Valeria Mateos
Jessica Heap
Nicolas G. Bazan
New Retinal Pigment Epithelial Cell Model to Unravel Neuroprotection Sensors of Neurodegeneration in Retinal Disease
Frontiers in Neuroscience
neuroprotectin D1
RPE cell
single cell
gene expression
lipids
apoptosis
title New Retinal Pigment Epithelial Cell Model to Unravel Neuroprotection Sensors of Neurodegeneration in Retinal Disease
title_full New Retinal Pigment Epithelial Cell Model to Unravel Neuroprotection Sensors of Neurodegeneration in Retinal Disease
title_fullStr New Retinal Pigment Epithelial Cell Model to Unravel Neuroprotection Sensors of Neurodegeneration in Retinal Disease
title_full_unstemmed New Retinal Pigment Epithelial Cell Model to Unravel Neuroprotection Sensors of Neurodegeneration in Retinal Disease
title_short New Retinal Pigment Epithelial Cell Model to Unravel Neuroprotection Sensors of Neurodegeneration in Retinal Disease
title_sort new retinal pigment epithelial cell model to unravel neuroprotection sensors of neurodegeneration in retinal disease
topic neuroprotectin D1
RPE cell
single cell
gene expression
lipids
apoptosis
url https://www.frontiersin.org/articles/10.3389/fnins.2022.926629/full
work_keys_str_mv AT aramasatryan newretinalpigmentepithelialcellmodeltounravelneuroprotectionsensorsofneurodegenerationinretinaldisease
AT jorgelinamcalandria newretinalpigmentepithelialcellmodeltounravelneuroprotectionsensorsofneurodegenerationinretinaldisease
AT marieaudreyikautzmann newretinalpigmentepithelialcellmodeltounravelneuroprotectionsensorsofneurodegenerationinretinaldisease
AT bokkyoojun newretinalpigmentepithelialcellmodeltounravelneuroprotectionsensorsofneurodegenerationinretinaldisease
AT williamcgordon newretinalpigmentepithelialcellmodeltounravelneuroprotectionsensorsofneurodegenerationinretinaldisease
AT khanhvdo newretinalpigmentepithelialcellmodeltounravelneuroprotectionsensorsofneurodegenerationinretinaldisease
AT surjyadiptabhattacharjee newretinalpigmentepithelialcellmodeltounravelneuroprotectionsensorsofneurodegenerationinretinaldisease
AT thanglpham newretinalpigmentepithelialcellmodeltounravelneuroprotectionsensorsofneurodegenerationinretinaldisease
AT vicentebermudez newretinalpigmentepithelialcellmodeltounravelneuroprotectionsensorsofneurodegenerationinretinaldisease
AT melinavaleriamateos newretinalpigmentepithelialcellmodeltounravelneuroprotectionsensorsofneurodegenerationinretinaldisease
AT jessicaheap newretinalpigmentepithelialcellmodeltounravelneuroprotectionsensorsofneurodegenerationinretinaldisease
AT nicolasgbazan newretinalpigmentepithelialcellmodeltounravelneuroprotectionsensorsofneurodegenerationinretinaldisease