Cargando…

Maturation of Neural Cells Leads to Enhanced Axon-Extracellular Matrix Adhesion and Altered Injury Response

Although it is known that stronger cell-extracellular matrix interactions will be developed as neurons mature, how such change influences their response against traumatic injury remains largely unknown. In this report, by transecting axons with a sharp atomic force microscope tip, we showed that the...

Descripción completa

Detalles Bibliográficos
Autores principales: Shao, Xueying, Sørensen, Maja Højvang, Fang, Chao, Chang, Raymond Chuen Chung, Chu, Zhiqin, Lin, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815929/
https://www.ncbi.nlm.nih.gov/pubmed/33490057
http://dx.doi.org/10.3389/fbioe.2020.621777
_version_ 1783638337848868864
author Shao, Xueying
Sørensen, Maja Højvang
Fang, Chao
Chang, Raymond Chuen Chung
Chu, Zhiqin
Lin, Yuan
author_facet Shao, Xueying
Sørensen, Maja Højvang
Fang, Chao
Chang, Raymond Chuen Chung
Chu, Zhiqin
Lin, Yuan
author_sort Shao, Xueying
collection PubMed
description Although it is known that stronger cell-extracellular matrix interactions will be developed as neurons mature, how such change influences their response against traumatic injury remains largely unknown. In this report, by transecting axons with a sharp atomic force microscope tip, we showed that the injury-induced retracting motion of axon can be temporarily arrested by tight NCAM (neural cell adhesion molecule) mediated adhesion patches, leading to a retraction curve decorated with sudden bursts. Interestingly, although the size of adhesion clusters (~0.5–1 μm) was found to be more or less the same in mature and immature neurons (after 7- and 3-days of culturing, respectively), the areal density of such clusters is three times higher in mature axons resulting in a much reduced retraction in response to injury. A physical model was also adopted to explain the observed retraction trajectories which suggested that apparent adhesion energy between axon and the substrate increases from ~0.12 to 0.39 mJ/m(2) as neural cell matures, in good agreement with our experiments.
format Online
Article
Text
id pubmed-7815929
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-78159292021-01-21 Maturation of Neural Cells Leads to Enhanced Axon-Extracellular Matrix Adhesion and Altered Injury Response Shao, Xueying Sørensen, Maja Højvang Fang, Chao Chang, Raymond Chuen Chung Chu, Zhiqin Lin, Yuan Front Bioeng Biotechnol Bioengineering and Biotechnology Although it is known that stronger cell-extracellular matrix interactions will be developed as neurons mature, how such change influences their response against traumatic injury remains largely unknown. In this report, by transecting axons with a sharp atomic force microscope tip, we showed that the injury-induced retracting motion of axon can be temporarily arrested by tight NCAM (neural cell adhesion molecule) mediated adhesion patches, leading to a retraction curve decorated with sudden bursts. Interestingly, although the size of adhesion clusters (~0.5–1 μm) was found to be more or less the same in mature and immature neurons (after 7- and 3-days of culturing, respectively), the areal density of such clusters is three times higher in mature axons resulting in a much reduced retraction in response to injury. A physical model was also adopted to explain the observed retraction trajectories which suggested that apparent adhesion energy between axon and the substrate increases from ~0.12 to 0.39 mJ/m(2) as neural cell matures, in good agreement with our experiments. Frontiers Media S.A. 2021-01-06 /pmc/articles/PMC7815929/ /pubmed/33490057 http://dx.doi.org/10.3389/fbioe.2020.621777 Text en Copyright © 2021 Shao, Sørensen, Fang, Chang, Chu and Lin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Shao, Xueying
Sørensen, Maja Højvang
Fang, Chao
Chang, Raymond Chuen Chung
Chu, Zhiqin
Lin, Yuan
Maturation of Neural Cells Leads to Enhanced Axon-Extracellular Matrix Adhesion and Altered Injury Response
title Maturation of Neural Cells Leads to Enhanced Axon-Extracellular Matrix Adhesion and Altered Injury Response
title_full Maturation of Neural Cells Leads to Enhanced Axon-Extracellular Matrix Adhesion and Altered Injury Response
title_fullStr Maturation of Neural Cells Leads to Enhanced Axon-Extracellular Matrix Adhesion and Altered Injury Response
title_full_unstemmed Maturation of Neural Cells Leads to Enhanced Axon-Extracellular Matrix Adhesion and Altered Injury Response
title_short Maturation of Neural Cells Leads to Enhanced Axon-Extracellular Matrix Adhesion and Altered Injury Response
title_sort maturation of neural cells leads to enhanced axon-extracellular matrix adhesion and altered injury response
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815929/
https://www.ncbi.nlm.nih.gov/pubmed/33490057
http://dx.doi.org/10.3389/fbioe.2020.621777
work_keys_str_mv AT shaoxueying maturationofneuralcellsleadstoenhancedaxonextracellularmatrixadhesionandalteredinjuryresponse
AT sørensenmajahøjvang maturationofneuralcellsleadstoenhancedaxonextracellularmatrixadhesionandalteredinjuryresponse
AT fangchao maturationofneuralcellsleadstoenhancedaxonextracellularmatrixadhesionandalteredinjuryresponse
AT changraymondchuenchung maturationofneuralcellsleadstoenhancedaxonextracellularmatrixadhesionandalteredinjuryresponse
AT chuzhiqin maturationofneuralcellsleadstoenhancedaxonextracellularmatrixadhesionandalteredinjuryresponse
AT linyuan maturationofneuralcellsleadstoenhancedaxonextracellularmatrixadhesionandalteredinjuryresponse