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携带自组装肽支架的人癫痫脑组织来源神经干细胞/前体细胞移植对大鼠脊髓损伤的改善作用。

Improvement of Rat Spinal Cord Injury Following Lentiviral Vector-Transduced Neural Stem/Progenitor Cells Derived from Human Epileptic Brain Tissue Transplantation with a Self-assembling Peptide Scaffold.

机构信息

Department of Pathobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.

Shefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran.

出版信息

Mol Neurobiol. 2021 Jun;58(6):2481-2493. doi: 10.1007/s12035-020-02279-5. Epub 2021 Jan 14.

DOI:10.1007/s12035-020-02279-5
PMID:33443682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8128971/
Abstract

Spinal cord injury (SCI) is a disabling neurological disorder that causes neural circuit dysfunction. Although various therapies have been applied to improve the neurological outcomes of SCI, little clinical progress has been achieved. Stem cell-based therapy aimed at restoring the lost cells and supporting micromilieu at the site of the injury has become a conceptually attractive option for tissue repair following SCI. Adult human neural stem/progenitor cells (hNS/PCs) were obtained from the epileptic human brain specimens. Induction of SCI was followed by the application of lentiviral vector-mediated green fluorescent protein-labeled hNS/PCs seeded in PuraMatrix peptide hydrogel (PM). The co-application of hNS/PCs and PM at the SCI injury site significantly enhanced cell survival and differentiation, reduced the lesion volume, and improved neurological functions compared to the control groups. Besides, the transplanted hNS/PCs seeded in PM revealed significantly higher migration abilities into the lesion site and the healthy host tissue as well as a greater differentiation into astrocytes and neurons in the vicinity of the lesion as well as in the host tissue. Our data suggest that the transplantation of hNS/PCs seeded in PM could be a promising approach to restore the damaged tissues and improve neurological functions after SCI.

摘要

脊髓损伤 (SCI) 是一种使人丧失能力的神经障碍,会导致神经回路功能障碍。尽管已经应用了各种疗法来改善 SCI 的神经预后,但临床进展甚微。基于干细胞的疗法旨在恢复受损部位丧失的细胞并支持微环境,已成为 SCI 后组织修复的一种具有吸引力的概念选择。从癫痫患者的大脑标本中获得成人人类神经干细胞/祖细胞 (hNS/PCs)。随后进行 SCI 诱导,然后将慢病毒载体介导的绿色荧光蛋白标记的 hNS/PCs 接种在 PuraMatrix 肽水凝胶 (PM) 中。与对照组相比,hNS/PC 与 PM 在 SCI 损伤部位的共同应用显著提高了细胞存活率和分化率,减少了损伤体积,并改善了神经功能。此外,接种在 PM 中的移植 hNS/PC 显示出向损伤部位和健康宿主组织的更高迁移能力,以及在损伤部位和宿主组织附近向星形胶质细胞和神经元的更大分化。我们的数据表明,PM 中接种的 hNS/PC 移植可能是一种很有前途的方法,可以在 SCI 后恢复受损组织并改善神经功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/4d799e5c314c/12035_2020_2279_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/1cdd8ec67884/12035_2020_2279_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/9028061439c9/12035_2020_2279_Fig2_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/30f763022504/12035_2020_2279_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/0265ec8f3ac1/12035_2020_2279_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/076de313d288/12035_2020_2279_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/c414779ce1d6/12035_2020_2279_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/05774a61ead4/12035_2020_2279_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/bb69a258cdd5/12035_2020_2279_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/4d799e5c314c/12035_2020_2279_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/1cdd8ec67884/12035_2020_2279_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/9028061439c9/12035_2020_2279_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/1bc2d4d1bbe2/12035_2020_2279_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/30f763022504/12035_2020_2279_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/0265ec8f3ac1/12035_2020_2279_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/076de313d288/12035_2020_2279_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/c414779ce1d6/12035_2020_2279_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/05774a61ead4/12035_2020_2279_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/bb69a258cdd5/12035_2020_2279_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8493/8128971/4d799e5c314c/12035_2020_2279_Fig10_HTML.jpg

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