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Macrophage-like cells are still detectable on the retinal surface after posterior vitreous detachment
The identity of vitreoretinal interface macrophage-like cells (MLCs) remains unknown and potential candidates include retinal microglia, perivascular macrophages, monocyte-derived macrophages, and/or vitreal hyalocytes. Since hyalocytes are detectable on the posterior vitreous surface after vitreous...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329361/ https://www.ncbi.nlm.nih.gov/pubmed/35896600 http://dx.doi.org/10.1038/s41598-022-17229-5 |
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author | Wang, Jacob M. Ong, Janice X. Nesper, Peter L. Fawzi, Amani A. Lavine, Jeremy A. |
author_facet | Wang, Jacob M. Ong, Janice X. Nesper, Peter L. Fawzi, Amani A. Lavine, Jeremy A. |
author_sort | Wang, Jacob M. |
collection | PubMed |
description | The identity of vitreoretinal interface macrophage-like cells (MLCs) remains unknown and potential candidates include retinal microglia, perivascular macrophages, monocyte-derived macrophages, and/or vitreal hyalocytes. Since hyalocytes are detectable on the posterior vitreous surface after vitreous extraction in animals, we imaged patients with and without posterior vitreous detachment (PVD) to determine if hyalocytes are the principal MLC component. We performed repeated foveal-centered 3 × 3 mm OCT-A images from 21 eyes (11 no PVD and 10 PVD eyes). Images were registered, segmented, and averaged. The OCT slab from 0 to 3 microns above the internal limiting membrane was used to detect MLCs. We calculated MLC density and distribution in relation to the superficial vascular plexus for 3 vascular regions—on vessels, perivascular, and non-vascular. MLC density was 1.8-fold greater in the PVD group compared to the no PVD group (P = 0.04). MLCs in eyes with PVD were increased 1.9-fold on-vessel (P = 0.07), 1.9-fold in the perivascular region (P = 0.12), and 2.2-fold in non-vascular areas (P = 0.22). MLC density was not severely reduced after PVD, suggesting that the majority of MLCs are not vitreal hyalocytes. PVD status is an important parameter in future MLC studies. |
format | Online Article Text |
id | pubmed-9329361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93293612022-07-29 Macrophage-like cells are still detectable on the retinal surface after posterior vitreous detachment Wang, Jacob M. Ong, Janice X. Nesper, Peter L. Fawzi, Amani A. Lavine, Jeremy A. Sci Rep Article The identity of vitreoretinal interface macrophage-like cells (MLCs) remains unknown and potential candidates include retinal microglia, perivascular macrophages, monocyte-derived macrophages, and/or vitreal hyalocytes. Since hyalocytes are detectable on the posterior vitreous surface after vitreous extraction in animals, we imaged patients with and without posterior vitreous detachment (PVD) to determine if hyalocytes are the principal MLC component. We performed repeated foveal-centered 3 × 3 mm OCT-A images from 21 eyes (11 no PVD and 10 PVD eyes). Images were registered, segmented, and averaged. The OCT slab from 0 to 3 microns above the internal limiting membrane was used to detect MLCs. We calculated MLC density and distribution in relation to the superficial vascular plexus for 3 vascular regions—on vessels, perivascular, and non-vascular. MLC density was 1.8-fold greater in the PVD group compared to the no PVD group (P = 0.04). MLCs in eyes with PVD were increased 1.9-fold on-vessel (P = 0.07), 1.9-fold in the perivascular region (P = 0.12), and 2.2-fold in non-vascular areas (P = 0.22). MLC density was not severely reduced after PVD, suggesting that the majority of MLCs are not vitreal hyalocytes. PVD status is an important parameter in future MLC studies. Nature Publishing Group UK 2022-07-27 /pmc/articles/PMC9329361/ /pubmed/35896600 http://dx.doi.org/10.1038/s41598-022-17229-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wang, Jacob M. Ong, Janice X. Nesper, Peter L. Fawzi, Amani A. Lavine, Jeremy A. Macrophage-like cells are still detectable on the retinal surface after posterior vitreous detachment |
title | Macrophage-like cells are still detectable on the retinal surface after posterior vitreous detachment |
title_full | Macrophage-like cells are still detectable on the retinal surface after posterior vitreous detachment |
title_fullStr | Macrophage-like cells are still detectable on the retinal surface after posterior vitreous detachment |
title_full_unstemmed | Macrophage-like cells are still detectable on the retinal surface after posterior vitreous detachment |
title_short | Macrophage-like cells are still detectable on the retinal surface after posterior vitreous detachment |
title_sort | macrophage-like cells are still detectable on the retinal surface after posterior vitreous detachment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329361/ https://www.ncbi.nlm.nih.gov/pubmed/35896600 http://dx.doi.org/10.1038/s41598-022-17229-5 |
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