Cargando…
The age factor in optic nerve regeneration: Intrinsic and extrinsic barriers hinder successful recovery in the short‐living killifish
As the mammalian central nervous system matures, its regenerative ability decreases, leading to incomplete or non‐recovery from the neurodegenerative diseases and central nervous system insults that we are increasingly facing in our aging world population. Current neuroregenerative research is large...
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/PMC8761009/ https://www.ncbi.nlm.nih.gov/pubmed/34927348 http://dx.doi.org/10.1111/acel.13537 |
_version_ | 1784633444156833792 |
---|---|
author | Vanhunsel, Sophie Bergmans, Steven Beckers, An Etienne, Isabelle Van Bergen, Tine De Groef, Lies Moons, Lieve |
author_facet | Vanhunsel, Sophie Bergmans, Steven Beckers, An Etienne, Isabelle Van Bergen, Tine De Groef, Lies Moons, Lieve |
author_sort | Vanhunsel, Sophie |
collection | PubMed |
description | As the mammalian central nervous system matures, its regenerative ability decreases, leading to incomplete or non‐recovery from the neurodegenerative diseases and central nervous system insults that we are increasingly facing in our aging world population. Current neuroregenerative research is largely directed toward identifying the molecular and cellular players that underlie central nervous system repair, yet it repeatedly ignores the aging context in which many of these diseases appear. Using an optic nerve crush model in a novel biogerontology model, that is, the short‐living African turquoise killifish, the impact of aging on injury‐induced optic nerve repair was investigated. This work reveals an age‐related decline in axonal regeneration in female killifish, with different phases of the repair process being affected depending on the age. Interestingly, as in mammals, both a reduced intrinsic growth potential and a non‐supportive cellular environment seem to lie at the basis of this impairment. Overall, we introduce the killifish visual system and its age‐dependent regenerative ability as a model to identify new targets for neurorepair in non‐regenerating individuals, thereby also considering the effects of aging on neurorepair. |
format | Online Article Text |
id | pubmed-8761009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87610092022-01-20 The age factor in optic nerve regeneration: Intrinsic and extrinsic barriers hinder successful recovery in the short‐living killifish Vanhunsel, Sophie Bergmans, Steven Beckers, An Etienne, Isabelle Van Bergen, Tine De Groef, Lies Moons, Lieve Aging Cell Original Papers As the mammalian central nervous system matures, its regenerative ability decreases, leading to incomplete or non‐recovery from the neurodegenerative diseases and central nervous system insults that we are increasingly facing in our aging world population. Current neuroregenerative research is largely directed toward identifying the molecular and cellular players that underlie central nervous system repair, yet it repeatedly ignores the aging context in which many of these diseases appear. Using an optic nerve crush model in a novel biogerontology model, that is, the short‐living African turquoise killifish, the impact of aging on injury‐induced optic nerve repair was investigated. This work reveals an age‐related decline in axonal regeneration in female killifish, with different phases of the repair process being affected depending on the age. Interestingly, as in mammals, both a reduced intrinsic growth potential and a non‐supportive cellular environment seem to lie at the basis of this impairment. Overall, we introduce the killifish visual system and its age‐dependent regenerative ability as a model to identify new targets for neurorepair in non‐regenerating individuals, thereby also considering the effects of aging on neurorepair. John Wiley and Sons Inc. 2021-12-19 2022-01 /pmc/articles/PMC8761009/ /pubmed/34927348 http://dx.doi.org/10.1111/acel.13537 Text en © 2021 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Vanhunsel, Sophie Bergmans, Steven Beckers, An Etienne, Isabelle Van Bergen, Tine De Groef, Lies Moons, Lieve The age factor in optic nerve regeneration: Intrinsic and extrinsic barriers hinder successful recovery in the short‐living killifish |
title | The age factor in optic nerve regeneration: Intrinsic and extrinsic barriers hinder successful recovery in the short‐living killifish |
title_full | The age factor in optic nerve regeneration: Intrinsic and extrinsic barriers hinder successful recovery in the short‐living killifish |
title_fullStr | The age factor in optic nerve regeneration: Intrinsic and extrinsic barriers hinder successful recovery in the short‐living killifish |
title_full_unstemmed | The age factor in optic nerve regeneration: Intrinsic and extrinsic barriers hinder successful recovery in the short‐living killifish |
title_short | The age factor in optic nerve regeneration: Intrinsic and extrinsic barriers hinder successful recovery in the short‐living killifish |
title_sort | age factor in optic nerve regeneration: intrinsic and extrinsic barriers hinder successful recovery in the short‐living killifish |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8761009/ https://www.ncbi.nlm.nih.gov/pubmed/34927348 http://dx.doi.org/10.1111/acel.13537 |
work_keys_str_mv | AT vanhunselsophie theagefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish AT bergmanssteven theagefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish AT beckersan theagefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish AT etienneisabelle theagefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish AT vanbergentine theagefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish AT degroeflies theagefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish AT moonslieve theagefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish AT vanhunselsophie agefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish AT bergmanssteven agefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish AT beckersan agefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish AT etienneisabelle agefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish AT vanbergentine agefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish AT degroeflies agefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish AT moonslieve agefactorinopticnerveregenerationintrinsicandextrinsicbarriershindersuccessfulrecoveryintheshortlivingkillifish |