Cargando…

Antibiotic-Induced Dysbiosis of Gut Microbiota Impairs Corneal Nerve Regeneration by Affecting CCR2-Negative Macrophage Distribution

Although antibiotics are useful, they can also bring negative effects. We found that antibiotic-treated mice exhibit an alteration in the gene expression profile of corneal tissues and a decrease in corneal nerve density. During corneal wound healing, antibiotic treatment was found to impair corneal...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Jun, Wu, Mingjuan, He, Jingxin, Xiao, Chengju, Xue, Yunxia, Fu, Ting, Lin, Cuipei, Dong, Dong, Li, Zhijie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Investigative Pathology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284554/
https://www.ncbi.nlm.nih.gov/pubmed/30470496
http://dx.doi.org/10.1016/j.ajpath.2018.08.009
_version_ 1783379353366691840
author Liu, Jun
Wu, Mingjuan
He, Jingxin
Xiao, Chengju
Xue, Yunxia
Fu, Ting
Lin, Cuipei
Dong, Dong
Li, Zhijie
author_facet Liu, Jun
Wu, Mingjuan
He, Jingxin
Xiao, Chengju
Xue, Yunxia
Fu, Ting
Lin, Cuipei
Dong, Dong
Li, Zhijie
author_sort Liu, Jun
collection PubMed
description Although antibiotics are useful, they can also bring negative effects. We found that antibiotic-treated mice exhibit an alteration in the gene expression profile of corneal tissues and a decrease in corneal nerve density. During corneal wound healing, antibiotic treatment was found to impair corneal nerve regeneration, an effect that could be largely reversed by reconstitution of the gut microbiota via fecal transplant. Furthermore, CCR2(−) corneal macrophages were found to participate in the repair of damaged corneal nerves, and a decrease in CCR2(−) corneal macrophages in antibiotic-treated mice, which could be reversed by fecal transplant, was observed. Adoptive transfer of CCR2(−) corneal macrophages promoted corneal nerve regeneration in antibiotic-treated mice. The application of probiotics after administration of antibiotics also restored the proportion of CCR2(−) corneal macrophages and increased the regeneration of corneal nerve fibers after epithelial abrasion. These results suggest that dysbiosis of the gut microbiota induced by antibiotic treatment impairs corneal nerve regeneration by affecting CCR2(−) macrophage distribution in the cornea. This study also indicates the potential of probiotics as a therapeutic strategy for promoting the regeneration of damaged corneal nerve fibers when the gut microbiota is in dysbiosis.
format Online
Article
Text
id pubmed-6284554
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher American Society for Investigative Pathology
record_format MEDLINE/PubMed
spelling pubmed-62845542019-12-01 Antibiotic-Induced Dysbiosis of Gut Microbiota Impairs Corneal Nerve Regeneration by Affecting CCR2-Negative Macrophage Distribution Liu, Jun Wu, Mingjuan He, Jingxin Xiao, Chengju Xue, Yunxia Fu, Ting Lin, Cuipei Dong, Dong Li, Zhijie Am J Pathol Article Although antibiotics are useful, they can also bring negative effects. We found that antibiotic-treated mice exhibit an alteration in the gene expression profile of corneal tissues and a decrease in corneal nerve density. During corneal wound healing, antibiotic treatment was found to impair corneal nerve regeneration, an effect that could be largely reversed by reconstitution of the gut microbiota via fecal transplant. Furthermore, CCR2(−) corneal macrophages were found to participate in the repair of damaged corneal nerves, and a decrease in CCR2(−) corneal macrophages in antibiotic-treated mice, which could be reversed by fecal transplant, was observed. Adoptive transfer of CCR2(−) corneal macrophages promoted corneal nerve regeneration in antibiotic-treated mice. The application of probiotics after administration of antibiotics also restored the proportion of CCR2(−) corneal macrophages and increased the regeneration of corneal nerve fibers after epithelial abrasion. These results suggest that dysbiosis of the gut microbiota induced by antibiotic treatment impairs corneal nerve regeneration by affecting CCR2(−) macrophage distribution in the cornea. This study also indicates the potential of probiotics as a therapeutic strategy for promoting the regeneration of damaged corneal nerve fibers when the gut microbiota is in dysbiosis. American Society for Investigative Pathology 2018-12 /pmc/articles/PMC6284554/ /pubmed/30470496 http://dx.doi.org/10.1016/j.ajpath.2018.08.009 Text en © 2018 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Liu, Jun
Wu, Mingjuan
He, Jingxin
Xiao, Chengju
Xue, Yunxia
Fu, Ting
Lin, Cuipei
Dong, Dong
Li, Zhijie
Antibiotic-Induced Dysbiosis of Gut Microbiota Impairs Corneal Nerve Regeneration by Affecting CCR2-Negative Macrophage Distribution
title Antibiotic-Induced Dysbiosis of Gut Microbiota Impairs Corneal Nerve Regeneration by Affecting CCR2-Negative Macrophage Distribution
title_full Antibiotic-Induced Dysbiosis of Gut Microbiota Impairs Corneal Nerve Regeneration by Affecting CCR2-Negative Macrophage Distribution
title_fullStr Antibiotic-Induced Dysbiosis of Gut Microbiota Impairs Corneal Nerve Regeneration by Affecting CCR2-Negative Macrophage Distribution
title_full_unstemmed Antibiotic-Induced Dysbiosis of Gut Microbiota Impairs Corneal Nerve Regeneration by Affecting CCR2-Negative Macrophage Distribution
title_short Antibiotic-Induced Dysbiosis of Gut Microbiota Impairs Corneal Nerve Regeneration by Affecting CCR2-Negative Macrophage Distribution
title_sort antibiotic-induced dysbiosis of gut microbiota impairs corneal nerve regeneration by affecting ccr2-negative macrophage distribution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284554/
https://www.ncbi.nlm.nih.gov/pubmed/30470496
http://dx.doi.org/10.1016/j.ajpath.2018.08.009
work_keys_str_mv AT liujun antibioticinduceddysbiosisofgutmicrobiotaimpairscornealnerveregenerationbyaffectingccr2negativemacrophagedistribution
AT wumingjuan antibioticinduceddysbiosisofgutmicrobiotaimpairscornealnerveregenerationbyaffectingccr2negativemacrophagedistribution
AT hejingxin antibioticinduceddysbiosisofgutmicrobiotaimpairscornealnerveregenerationbyaffectingccr2negativemacrophagedistribution
AT xiaochengju antibioticinduceddysbiosisofgutmicrobiotaimpairscornealnerveregenerationbyaffectingccr2negativemacrophagedistribution
AT xueyunxia antibioticinduceddysbiosisofgutmicrobiotaimpairscornealnerveregenerationbyaffectingccr2negativemacrophagedistribution
AT futing antibioticinduceddysbiosisofgutmicrobiotaimpairscornealnerveregenerationbyaffectingccr2negativemacrophagedistribution
AT lincuipei antibioticinduceddysbiosisofgutmicrobiotaimpairscornealnerveregenerationbyaffectingccr2negativemacrophagedistribution
AT dongdong antibioticinduceddysbiosisofgutmicrobiotaimpairscornealnerveregenerationbyaffectingccr2negativemacrophagedistribution
AT lizhijie antibioticinduceddysbiosisofgutmicrobiotaimpairscornealnerveregenerationbyaffectingccr2negativemacrophagedistribution