Design and Fabrication of Nanofibrous Dura Mater with Antifibrosis and Neuroprotection Effects on SH-SY5Y Cells

The development and treatment of some diseases, such as large-area cerebral infarction, cerebral hemorrhage, brain tumor, and craniocerebral trauma, which may involve the injury of the dura mater, elicit the need to repair this membrane by dural grafts. However, common dural grafts tend to result in...

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Main Authors: Zhiyuan Zhao, Tong Wu, Yu Cui, Rui Zhao, Qi Wan, Rui Xu
Format: Article
Language:English
Published: MDPI AG 2022-05-01
Series:Polymers
Subjects:
Online Access:https://www.mdpi.com/2073-4360/14/9/1882
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author Zhiyuan Zhao
Tong Wu
Yu Cui
Rui Zhao
Qi Wan
Rui Xu
author_facet Zhiyuan Zhao
Tong Wu
Yu Cui
Rui Zhao
Qi Wan
Rui Xu
author_sort Zhiyuan Zhao
collection DOAJ
description The development and treatment of some diseases, such as large-area cerebral infarction, cerebral hemorrhage, brain tumor, and craniocerebral trauma, which may involve the injury of the dura mater, elicit the need to repair this membrane by dural grafts. However, common dural grafts tend to result in dural adhesions and scar tissue and have no further neuroprotective effects. In order to reduce or avoid the complications of dural repair, we used PLGA, tetramethylpyrazine, and chitosan as raw materials to prepare a nanofibrous dura mater (NDM) with excellent biocompatibility and adequate mechanical characteristics, which can play a neuroprotective role and have an antifibrotic effect. We fabricated PLGA NDM by electrospinning, and then chitosan was grafted on the nanofibrous dura mater by the EDC-NHS cross-linking method to obtain PLGA/CS NDM. Then, we also prepared PLGA/TMP/CS NDM by coaxial electrospinning. Our study shows that the PLGA/TMP/CS NDM can inhibit the excessive proliferation of fibroblasts, as well as provide a sustained protective effect on the SH-SY5Y cells treated with oxygen–glucose deprivation/reperfusion (OGD/R). In conclusion, our study may provide a new alternative to dural grafts in undesirable cases of dural injuries.
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spelling doaj.art-e145de36b49d4bf5a8c5e6e4673832a82023-11-23T09:07:39ZengMDPI AGPolymers2073-43602022-05-01149188210.3390/polym14091882Design and Fabrication of Nanofibrous Dura Mater with Antifibrosis and Neuroprotection Effects on SH-SY5Y CellsZhiyuan Zhao0Tong Wu1Yu Cui2Rui Zhao3Qi Wan4Rui Xu5Department of Interventional Radiology, The Affiliated Hospital of Qingdao University, Jiangsu Road 16, Qingdao 266000, ChinaInstitute of Neuroregeneration and Neurorehabilitation, Qingdao University, Qingdao 266071, ChinaInstitute of Neuroregeneration and Neurorehabilitation, Qingdao University, Qingdao 266071, ChinaDepartment of Interventional Radiology, The Affiliated Hospital of Qingdao University, Jiangsu Road 16, Qingdao 266000, ChinaInstitute of Neuroregeneration and Neurorehabilitation, Qingdao University, Qingdao 266071, ChinaDepartment of Interventional Radiology, The Affiliated Hospital of Qingdao University, Jiangsu Road 16, Qingdao 266000, ChinaThe development and treatment of some diseases, such as large-area cerebral infarction, cerebral hemorrhage, brain tumor, and craniocerebral trauma, which may involve the injury of the dura mater, elicit the need to repair this membrane by dural grafts. However, common dural grafts tend to result in dural adhesions and scar tissue and have no further neuroprotective effects. In order to reduce or avoid the complications of dural repair, we used PLGA, tetramethylpyrazine, and chitosan as raw materials to prepare a nanofibrous dura mater (NDM) with excellent biocompatibility and adequate mechanical characteristics, which can play a neuroprotective role and have an antifibrotic effect. We fabricated PLGA NDM by electrospinning, and then chitosan was grafted on the nanofibrous dura mater by the EDC-NHS cross-linking method to obtain PLGA/CS NDM. Then, we also prepared PLGA/TMP/CS NDM by coaxial electrospinning. Our study shows that the PLGA/TMP/CS NDM can inhibit the excessive proliferation of fibroblasts, as well as provide a sustained protective effect on the SH-SY5Y cells treated with oxygen–glucose deprivation/reperfusion (OGD/R). In conclusion, our study may provide a new alternative to dural grafts in undesirable cases of dural injuries.https://www.mdpi.com/2073-4360/14/9/1882nanofibrous dura materantifibrosisneuroprotectionPLGAtetramethylpyrazine
spellingShingle Zhiyuan Zhao
Tong Wu
Yu Cui
Rui Zhao
Qi Wan
Rui Xu
Design and Fabrication of Nanofibrous Dura Mater with Antifibrosis and Neuroprotection Effects on SH-SY5Y Cells
Polymers
nanofibrous dura mater
antifibrosis
neuroprotection
PLGA
tetramethylpyrazine
title Design and Fabrication of Nanofibrous Dura Mater with Antifibrosis and Neuroprotection Effects on SH-SY5Y Cells
title_full Design and Fabrication of Nanofibrous Dura Mater with Antifibrosis and Neuroprotection Effects on SH-SY5Y Cells
title_fullStr Design and Fabrication of Nanofibrous Dura Mater with Antifibrosis and Neuroprotection Effects on SH-SY5Y Cells
title_full_unstemmed Design and Fabrication of Nanofibrous Dura Mater with Antifibrosis and Neuroprotection Effects on SH-SY5Y Cells
title_short Design and Fabrication of Nanofibrous Dura Mater with Antifibrosis and Neuroprotection Effects on SH-SY5Y Cells
title_sort design and fabrication of nanofibrous dura mater with antifibrosis and neuroprotection effects on sh sy5y cells
topic nanofibrous dura mater
antifibrosis
neuroprotection
PLGA
tetramethylpyrazine
url https://www.mdpi.com/2073-4360/14/9/1882
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