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The Three-Dimensional Culture System with Matrigel and Neurotrophic Factors Preserves the Structure and Function of Spiral Ganglion Neuron In Vitro

Whole organ culture of the spiral ganglion region is a resourceful model system facilitating manipulation and analysis of live sprial ganglion neurons (SGNs). Three-dimensional (3D) cultures have been demonstrated to have many biomedical applications, but the effect of 3D culture in maintaining the...

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Autores principales: Sun, Gaoying, Liu, Wenwen, Fan, Zhaomin, Zhang, Daogong, Han, Yuechen, Xu, Lei, Qi, Jieyu, Zhang, Shasha, Gao, Bradley T., Bai, Xiaohui, Li, Jianfeng, Chai, Renjie, Wang, Haibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736769/
https://www.ncbi.nlm.nih.gov/pubmed/27057364
http://dx.doi.org/10.1155/2016/4280407
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author Sun, Gaoying
Liu, Wenwen
Fan, Zhaomin
Zhang, Daogong
Han, Yuechen
Xu, Lei
Qi, Jieyu
Zhang, Shasha
Gao, Bradley T.
Bai, Xiaohui
Li, Jianfeng
Chai, Renjie
Wang, Haibo
author_facet Sun, Gaoying
Liu, Wenwen
Fan, Zhaomin
Zhang, Daogong
Han, Yuechen
Xu, Lei
Qi, Jieyu
Zhang, Shasha
Gao, Bradley T.
Bai, Xiaohui
Li, Jianfeng
Chai, Renjie
Wang, Haibo
author_sort Sun, Gaoying
collection PubMed
description Whole organ culture of the spiral ganglion region is a resourceful model system facilitating manipulation and analysis of live sprial ganglion neurons (SGNs). Three-dimensional (3D) cultures have been demonstrated to have many biomedical applications, but the effect of 3D culture in maintaining the SGNs structure and function in explant culture remains uninvestigated. In this study, we used the matrigel to encapsulate the spiral ganglion region isolated from neonatal mice. First, we optimized the matrigel concentration for the 3D culture system and found the 3D culture system protected the SGNs against apoptosis, preserved the structure of spiral ganglion region, and promoted the sprouting and outgrowth of SGNs neurites. Next, we found the 3D culture system promoted growth cone growth as evidenced by a higher average number and a longer average length of filopodia and a larger growth cone area. 3D culture system also significantly elevated the synapse density of SGNs. Last, we found that the 3D culture system combined with neurotrophic factors had accumulated effects in promoting the neurites outgrowth compared with 3D culture or NFs treatment only groups. Together, we conclude that the 3D culture system preserves the structure and function of SGN in explant culture.
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spelling pubmed-47367692016-04-07 The Three-Dimensional Culture System with Matrigel and Neurotrophic Factors Preserves the Structure and Function of Spiral Ganglion Neuron In Vitro Sun, Gaoying Liu, Wenwen Fan, Zhaomin Zhang, Daogong Han, Yuechen Xu, Lei Qi, Jieyu Zhang, Shasha Gao, Bradley T. Bai, Xiaohui Li, Jianfeng Chai, Renjie Wang, Haibo Neural Plast Research Article Whole organ culture of the spiral ganglion region is a resourceful model system facilitating manipulation and analysis of live sprial ganglion neurons (SGNs). Three-dimensional (3D) cultures have been demonstrated to have many biomedical applications, but the effect of 3D culture in maintaining the SGNs structure and function in explant culture remains uninvestigated. In this study, we used the matrigel to encapsulate the spiral ganglion region isolated from neonatal mice. First, we optimized the matrigel concentration for the 3D culture system and found the 3D culture system protected the SGNs against apoptosis, preserved the structure of spiral ganglion region, and promoted the sprouting and outgrowth of SGNs neurites. Next, we found the 3D culture system promoted growth cone growth as evidenced by a higher average number and a longer average length of filopodia and a larger growth cone area. 3D culture system also significantly elevated the synapse density of SGNs. Last, we found that the 3D culture system combined with neurotrophic factors had accumulated effects in promoting the neurites outgrowth compared with 3D culture or NFs treatment only groups. Together, we conclude that the 3D culture system preserves the structure and function of SGN in explant culture. Hindawi Publishing Corporation 2016 2016-01-06 /pmc/articles/PMC4736769/ /pubmed/27057364 http://dx.doi.org/10.1155/2016/4280407 Text en Copyright © 2016 Gaoying Sun et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sun, Gaoying
Liu, Wenwen
Fan, Zhaomin
Zhang, Daogong
Han, Yuechen
Xu, Lei
Qi, Jieyu
Zhang, Shasha
Gao, Bradley T.
Bai, Xiaohui
Li, Jianfeng
Chai, Renjie
Wang, Haibo
The Three-Dimensional Culture System with Matrigel and Neurotrophic Factors Preserves the Structure and Function of Spiral Ganglion Neuron In Vitro
title The Three-Dimensional Culture System with Matrigel and Neurotrophic Factors Preserves the Structure and Function of Spiral Ganglion Neuron In Vitro
title_full The Three-Dimensional Culture System with Matrigel and Neurotrophic Factors Preserves the Structure and Function of Spiral Ganglion Neuron In Vitro
title_fullStr The Three-Dimensional Culture System with Matrigel and Neurotrophic Factors Preserves the Structure and Function of Spiral Ganglion Neuron In Vitro
title_full_unstemmed The Three-Dimensional Culture System with Matrigel and Neurotrophic Factors Preserves the Structure and Function of Spiral Ganglion Neuron In Vitro
title_short The Three-Dimensional Culture System with Matrigel and Neurotrophic Factors Preserves the Structure and Function of Spiral Ganglion Neuron In Vitro
title_sort three-dimensional culture system with matrigel and neurotrophic factors preserves the structure and function of spiral ganglion neuron in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736769/
https://www.ncbi.nlm.nih.gov/pubmed/27057364
http://dx.doi.org/10.1155/2016/4280407
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