Cargando…
Uveitis‐mediated immune cell invasion through the extracellular matrix of the lens capsule
While the eye is considered an immune privileged site, its privilege is abrogated when immune cells are recruited from the surrounding vasculature in response to trauma, infection, aging, and autoimmune diseases like uveitis. Here, we investigate whether in uveitis immune cells become associated wit...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300120/ https://www.ncbi.nlm.nih.gov/pubmed/34874579 http://dx.doi.org/10.1096/fj.202101098R |
_version_ | 1784751137657716736 |
---|---|
author | DeDreu, JodiRae Pal‐Ghosh, Sonali Mattapallil, Mary J. Caspi, Rachel R. Stepp, Mary Ann Menko, A. Sue |
author_facet | DeDreu, JodiRae Pal‐Ghosh, Sonali Mattapallil, Mary J. Caspi, Rachel R. Stepp, Mary Ann Menko, A. Sue |
author_sort | DeDreu, JodiRae |
collection | PubMed |
description | While the eye is considered an immune privileged site, its privilege is abrogated when immune cells are recruited from the surrounding vasculature in response to trauma, infection, aging, and autoimmune diseases like uveitis. Here, we investigate whether in uveitis immune cells become associated with the lens capsule and compromise its privilege in studies of C57BL/6J mice with experimental autoimmune uveitis. These studies show that at D14, the peak of uveitis in these mice, T cells, macrophages, and Ly6G/Ly6C+ immune cells associate with the lens basement membrane capsule, burrow into the capsule matrix, and remain integrated with the capsule as immune resolution is occurring at D26. 3D surface rendering image analytics of confocal z‐stacks and scanning electron microscopy imaging of the lens surface show the degradation of the lens capsule as these lens‐associated immune cells integrate with and invade the lens capsule, with a subset infiltrating both epithelial and fiber cell regions of lens tissue, abrogating its immune privilege. Those immune cells that remain on the surface often become entwined with a fibrillar net‐like structure. Immune cell invasion of the lens capsule in uveitis has not been described previously and may play a role in induction of lens and other eye pathologies associated with autoimmunity. |
format | Online Article Text |
id | pubmed-9300120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93001202022-07-21 Uveitis‐mediated immune cell invasion through the extracellular matrix of the lens capsule DeDreu, JodiRae Pal‐Ghosh, Sonali Mattapallil, Mary J. Caspi, Rachel R. Stepp, Mary Ann Menko, A. Sue FASEB J Research Articles While the eye is considered an immune privileged site, its privilege is abrogated when immune cells are recruited from the surrounding vasculature in response to trauma, infection, aging, and autoimmune diseases like uveitis. Here, we investigate whether in uveitis immune cells become associated with the lens capsule and compromise its privilege in studies of C57BL/6J mice with experimental autoimmune uveitis. These studies show that at D14, the peak of uveitis in these mice, T cells, macrophages, and Ly6G/Ly6C+ immune cells associate with the lens basement membrane capsule, burrow into the capsule matrix, and remain integrated with the capsule as immune resolution is occurring at D26. 3D surface rendering image analytics of confocal z‐stacks and scanning electron microscopy imaging of the lens surface show the degradation of the lens capsule as these lens‐associated immune cells integrate with and invade the lens capsule, with a subset infiltrating both epithelial and fiber cell regions of lens tissue, abrogating its immune privilege. Those immune cells that remain on the surface often become entwined with a fibrillar net‐like structure. Immune cell invasion of the lens capsule in uveitis has not been described previously and may play a role in induction of lens and other eye pathologies associated with autoimmunity. John Wiley and Sons Inc. 2021-12-07 2022-01 /pmc/articles/PMC9300120/ /pubmed/34874579 http://dx.doi.org/10.1096/fj.202101098R Text en © 2021 The Authors. The FASEB Journal published by Wiley Periodicals LLC on behalf of Federation of American Societies for Experimental Biology. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles DeDreu, JodiRae Pal‐Ghosh, Sonali Mattapallil, Mary J. Caspi, Rachel R. Stepp, Mary Ann Menko, A. Sue Uveitis‐mediated immune cell invasion through the extracellular matrix of the lens capsule |
title | Uveitis‐mediated immune cell invasion through the extracellular matrix of the lens capsule |
title_full | Uveitis‐mediated immune cell invasion through the extracellular matrix of the lens capsule |
title_fullStr | Uveitis‐mediated immune cell invasion through the extracellular matrix of the lens capsule |
title_full_unstemmed | Uveitis‐mediated immune cell invasion through the extracellular matrix of the lens capsule |
title_short | Uveitis‐mediated immune cell invasion through the extracellular matrix of the lens capsule |
title_sort | uveitis‐mediated immune cell invasion through the extracellular matrix of the lens capsule |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300120/ https://www.ncbi.nlm.nih.gov/pubmed/34874579 http://dx.doi.org/10.1096/fj.202101098R |
work_keys_str_mv | AT dedreujodirae uveitismediatedimmunecellinvasionthroughtheextracellularmatrixofthelenscapsule AT palghoshsonali uveitismediatedimmunecellinvasionthroughtheextracellularmatrixofthelenscapsule AT mattapallilmaryj uveitismediatedimmunecellinvasionthroughtheextracellularmatrixofthelenscapsule AT caspirachelr uveitismediatedimmunecellinvasionthroughtheextracellularmatrixofthelenscapsule AT steppmaryann uveitismediatedimmunecellinvasionthroughtheextracellularmatrixofthelenscapsule AT menkoasue uveitismediatedimmunecellinvasionthroughtheextracellularmatrixofthelenscapsule |