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3D spheroids of human placenta-derived mesenchymal stem cells attenuate spinal cord injury in mice

Mesenchymal stem cell (MSC) is an absorbing candidate for cell therapy in treating spinal cord injury (SCI) due to its great potential for multiple cell differentiation, mighty paracrine secretion as well as vigorous immunomodulatory effect, of which are beneficial to the improvement of functional r...

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Autores principales: Deng, Junhao, Li, Miao, Meng, Fanqi, Liu, Zhongyang, Wang, Song, Zhang, Yuan, Li, Ming, Li, Zhirui, Zhang, Licheng, Tang, Peifu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606575/
https://www.ncbi.nlm.nih.gov/pubmed/34803160
http://dx.doi.org/10.1038/s41419-021-04398-w
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author Deng, Junhao
Li, Miao
Meng, Fanqi
Liu, Zhongyang
Wang, Song
Zhang, Yuan
Li, Ming
Li, Zhirui
Zhang, Licheng
Tang, Peifu
author_facet Deng, Junhao
Li, Miao
Meng, Fanqi
Liu, Zhongyang
Wang, Song
Zhang, Yuan
Li, Ming
Li, Zhirui
Zhang, Licheng
Tang, Peifu
author_sort Deng, Junhao
collection PubMed
description Mesenchymal stem cell (MSC) is an absorbing candidate for cell therapy in treating spinal cord injury (SCI) due to its great potential for multiple cell differentiation, mighty paracrine secretion as well as vigorous immunomodulatory effect, of which are beneficial to the improvement of functional recovery post SCI. However, the therapeutic effects of MSC on SCI have been limited because of the gradual loss of MSC stemness in the process of expanding culture. Therefore, in this study, we aimed to maintain those beneficial properties of MSC via three-dimensional spheroid cell culture and then compared them with conventionally-cultured MSCs in the treatment of SCI both in vitro and in vivo with the aid of two-photon microscope. We found that 3D human placenta-derived MSCs (3D-HPMSCs) demonstrated a significant increase in secretion of anti-inflammatory factors and trophic factors like VEGF, PDGF, FGF via QPCR and Bio-Plex assays, and showed great potentials on angiogenesis and neurite morphogenesis when co-cultured with HUVECs or DRGs in vitro. After transplantation into the injured spinal cord, 3D-HPMSCs managed to survive for the entire experiment and retained their advantageous properties in secretion, and exhibited remarkable effects on neuroprotection by minimizing the lesion cavity, inhibiting the inflammation and astrogliosis, and promoting angiogenesis. Further investigation of axonal dieback via two-photon microscope indicated that 3D-HPMSCs could effectively alleviate axonal dieback post injury. Further, mice only treated with 3D-HPMSCs obtained substantial improvement of functional recovery on electrophysiology, BMS score, and Catwalk analysis. RNA sequencing suggested that the 3D-HPMSCs structure organization-related gene was significantly changed, which was likely to potentiate the angiogenesis and inflammation regulation after SCI. These results suggest that 3D-HPMSCs may hold great potential for the treatment of SCI.
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spelling pubmed-86065752021-12-03 3D spheroids of human placenta-derived mesenchymal stem cells attenuate spinal cord injury in mice Deng, Junhao Li, Miao Meng, Fanqi Liu, Zhongyang Wang, Song Zhang, Yuan Li, Ming Li, Zhirui Zhang, Licheng Tang, Peifu Cell Death Dis Article Mesenchymal stem cell (MSC) is an absorbing candidate for cell therapy in treating spinal cord injury (SCI) due to its great potential for multiple cell differentiation, mighty paracrine secretion as well as vigorous immunomodulatory effect, of which are beneficial to the improvement of functional recovery post SCI. However, the therapeutic effects of MSC on SCI have been limited because of the gradual loss of MSC stemness in the process of expanding culture. Therefore, in this study, we aimed to maintain those beneficial properties of MSC via three-dimensional spheroid cell culture and then compared them with conventionally-cultured MSCs in the treatment of SCI both in vitro and in vivo with the aid of two-photon microscope. We found that 3D human placenta-derived MSCs (3D-HPMSCs) demonstrated a significant increase in secretion of anti-inflammatory factors and trophic factors like VEGF, PDGF, FGF via QPCR and Bio-Plex assays, and showed great potentials on angiogenesis and neurite morphogenesis when co-cultured with HUVECs or DRGs in vitro. After transplantation into the injured spinal cord, 3D-HPMSCs managed to survive for the entire experiment and retained their advantageous properties in secretion, and exhibited remarkable effects on neuroprotection by minimizing the lesion cavity, inhibiting the inflammation and astrogliosis, and promoting angiogenesis. Further investigation of axonal dieback via two-photon microscope indicated that 3D-HPMSCs could effectively alleviate axonal dieback post injury. Further, mice only treated with 3D-HPMSCs obtained substantial improvement of functional recovery on electrophysiology, BMS score, and Catwalk analysis. RNA sequencing suggested that the 3D-HPMSCs structure organization-related gene was significantly changed, which was likely to potentiate the angiogenesis and inflammation regulation after SCI. These results suggest that 3D-HPMSCs may hold great potential for the treatment of SCI. Nature Publishing Group UK 2021-11-22 /pmc/articles/PMC8606575/ /pubmed/34803160 http://dx.doi.org/10.1038/s41419-021-04398-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Deng, Junhao
Li, Miao
Meng, Fanqi
Liu, Zhongyang
Wang, Song
Zhang, Yuan
Li, Ming
Li, Zhirui
Zhang, Licheng
Tang, Peifu
3D spheroids of human placenta-derived mesenchymal stem cells attenuate spinal cord injury in mice
title 3D spheroids of human placenta-derived mesenchymal stem cells attenuate spinal cord injury in mice
title_full 3D spheroids of human placenta-derived mesenchymal stem cells attenuate spinal cord injury in mice
title_fullStr 3D spheroids of human placenta-derived mesenchymal stem cells attenuate spinal cord injury in mice
title_full_unstemmed 3D spheroids of human placenta-derived mesenchymal stem cells attenuate spinal cord injury in mice
title_short 3D spheroids of human placenta-derived mesenchymal stem cells attenuate spinal cord injury in mice
title_sort 3d spheroids of human placenta-derived mesenchymal stem cells attenuate spinal cord injury in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606575/
https://www.ncbi.nlm.nih.gov/pubmed/34803160
http://dx.doi.org/10.1038/s41419-021-04398-w
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