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CCL2-mediated inflammatory pathogenesis underlies high myopia-related anxiety
High myopia is a leading cause of blindness worldwide. It may lead to emotional defects that rely closely on the link between visual sensation and the central nervous system. However, the extent of the defects and its underlying mechanism remain unknown. Here, we report that highly myopic patients e...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Nature Singapore
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497683/ https://www.ncbi.nlm.nih.gov/pubmed/37699875 http://dx.doi.org/10.1038/s41421-023-00588-2 |
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author | Zhu, Xiangjia Meng, Jiaqi Han, Chaofeng Wu, Qingfeng Du, Yu Qi, Jiao Wei, Ling Li, Hao He, Wenwen Zhang, Keke Lu, Yi |
author_facet | Zhu, Xiangjia Meng, Jiaqi Han, Chaofeng Wu, Qingfeng Du, Yu Qi, Jiao Wei, Ling Li, Hao He, Wenwen Zhang, Keke Lu, Yi |
author_sort | Zhu, Xiangjia |
collection | PubMed |
description | High myopia is a leading cause of blindness worldwide. It may lead to emotional defects that rely closely on the link between visual sensation and the central nervous system. However, the extent of the defects and its underlying mechanism remain unknown. Here, we report that highly myopic patients exhibit greater anxiety, accompanied by higher CC chemokine ligand 2 (CCL2) and monocyte levels in the blood. Similar findings are found in the mouse model of high myopia. Mechanistic evaluations using GFP-positive bone marrow chimeric mice, parabiotic mouse model, enhanced magnetic resonance imaging, etc., show that highly myopic visual stimulation increases CCL2 expression in eyes, aggravates monocyte/macrophage infiltration into eyes and brains, and disrupts blood–ocular barrier and blood–brain barrier of mice. Conversely, Ccl2-deficient highly myopic mice exhibit attenuated ocular and brain infiltration of monocytes/macrophages, reduced disruption of the blood–ocular barrier and blood–brain barrier, and less anxiety. Substantial alleviation of high myopia-related anxiety can also be achieved with the administration of CCL2-neutralizing antibodies. Our results establish the association between high myopia and anxiety, and implicate the CCL2-mediated inflammatory pathogenesis as an underlying mechanism. |
format | Online Article Text |
id | pubmed-10497683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Nature Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-104976832023-09-14 CCL2-mediated inflammatory pathogenesis underlies high myopia-related anxiety Zhu, Xiangjia Meng, Jiaqi Han, Chaofeng Wu, Qingfeng Du, Yu Qi, Jiao Wei, Ling Li, Hao He, Wenwen Zhang, Keke Lu, Yi Cell Discov Article High myopia is a leading cause of blindness worldwide. It may lead to emotional defects that rely closely on the link between visual sensation and the central nervous system. However, the extent of the defects and its underlying mechanism remain unknown. Here, we report that highly myopic patients exhibit greater anxiety, accompanied by higher CC chemokine ligand 2 (CCL2) and monocyte levels in the blood. Similar findings are found in the mouse model of high myopia. Mechanistic evaluations using GFP-positive bone marrow chimeric mice, parabiotic mouse model, enhanced magnetic resonance imaging, etc., show that highly myopic visual stimulation increases CCL2 expression in eyes, aggravates monocyte/macrophage infiltration into eyes and brains, and disrupts blood–ocular barrier and blood–brain barrier of mice. Conversely, Ccl2-deficient highly myopic mice exhibit attenuated ocular and brain infiltration of monocytes/macrophages, reduced disruption of the blood–ocular barrier and blood–brain barrier, and less anxiety. Substantial alleviation of high myopia-related anxiety can also be achieved with the administration of CCL2-neutralizing antibodies. Our results establish the association between high myopia and anxiety, and implicate the CCL2-mediated inflammatory pathogenesis as an underlying mechanism. Springer Nature Singapore 2023-09-12 /pmc/articles/PMC10497683/ /pubmed/37699875 http://dx.doi.org/10.1038/s41421-023-00588-2 Text en © The Author(s) 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhu, Xiangjia Meng, Jiaqi Han, Chaofeng Wu, Qingfeng Du, Yu Qi, Jiao Wei, Ling Li, Hao He, Wenwen Zhang, Keke Lu, Yi CCL2-mediated inflammatory pathogenesis underlies high myopia-related anxiety |
title | CCL2-mediated inflammatory pathogenesis underlies high myopia-related anxiety |
title_full | CCL2-mediated inflammatory pathogenesis underlies high myopia-related anxiety |
title_fullStr | CCL2-mediated inflammatory pathogenesis underlies high myopia-related anxiety |
title_full_unstemmed | CCL2-mediated inflammatory pathogenesis underlies high myopia-related anxiety |
title_short | CCL2-mediated inflammatory pathogenesis underlies high myopia-related anxiety |
title_sort | ccl2-mediated inflammatory pathogenesis underlies high myopia-related anxiety |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497683/ https://www.ncbi.nlm.nih.gov/pubmed/37699875 http://dx.doi.org/10.1038/s41421-023-00588-2 |
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