Cargando…
Transplanting Rac1-silenced bone marrow mesenchymal stem cells promote neurological function recovery in TBI mice
Bone marrow mesenchymal stem cells (BMMSCs)-based therapy has emerged as a promising novel therapy for Traumatic Brain Injury (TBI). However, the therapeutic quantity of viable implanted BMMSCs necessary to initiate efficacy is still undetermined. Increased oxidative stress following TBI, which lead...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880331/ https://www.ncbi.nlm.nih.gov/pubmed/33411679 http://dx.doi.org/10.18632/aging.202334 |
_version_ | 1783650680817319936 |
---|---|
author | Huang, Dongdong Siaw-Debrah, Felix Wang, Hua Ye, Sheng Wang, Kankai Wu, Ke Zhang, Ying Wang, Hao Yao, Chaojie Chen, Jiayu Yan, Lin Zhang, Chun-Li Zhuge, Qichuan Yang, Jianjing |
author_facet | Huang, Dongdong Siaw-Debrah, Felix Wang, Hua Ye, Sheng Wang, Kankai Wu, Ke Zhang, Ying Wang, Hao Yao, Chaojie Chen, Jiayu Yan, Lin Zhang, Chun-Li Zhuge, Qichuan Yang, Jianjing |
author_sort | Huang, Dongdong |
collection | PubMed |
description | Bone marrow mesenchymal stem cells (BMMSCs)-based therapy has emerged as a promising novel therapy for Traumatic Brain Injury (TBI). However, the therapeutic quantity of viable implanted BMMSCs necessary to initiate efficacy is still undetermined. Increased oxidative stress following TBI, which leads to the activation of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase signaling pathway, has been implicated in accounting for the diminished graft survival and therapeutic effect. To prove this assertion, we silenced the expression of NADPH subunits (p22-phox, p47-phox, and p67-phox) and small GTPase Rac1 in BMMSCs using shRNA. Our results showed that silencing these proteins significantly reduced oxidative stress and cell death/apoptosis, and promoted implanted BMMSCs proliferation after TBI. The most significant result was however seen with Rac1 silencing, which demonstrated decreased expression of apoptotic proteins, enhanced in vitro survival ratio, reduction in TBI lesional volume and significant improvement in neurological function post shRac1-BMMSCs transplantation. Additionally, two RNA-seq hub genes (VEGFA and MMP-2) were identified to play critical roles in shRac1-mediated cell survival. In summary, we propose that knockdown of Rac1 gene could significantly boost cell survival and promote the recovery of neurological functions after BMMSCs transplantation in TBI mice. |
format | Online Article Text |
id | pubmed-7880331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-78803312021-02-22 Transplanting Rac1-silenced bone marrow mesenchymal stem cells promote neurological function recovery in TBI mice Huang, Dongdong Siaw-Debrah, Felix Wang, Hua Ye, Sheng Wang, Kankai Wu, Ke Zhang, Ying Wang, Hao Yao, Chaojie Chen, Jiayu Yan, Lin Zhang, Chun-Li Zhuge, Qichuan Yang, Jianjing Aging (Albany NY) Research Paper Bone marrow mesenchymal stem cells (BMMSCs)-based therapy has emerged as a promising novel therapy for Traumatic Brain Injury (TBI). However, the therapeutic quantity of viable implanted BMMSCs necessary to initiate efficacy is still undetermined. Increased oxidative stress following TBI, which leads to the activation of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase signaling pathway, has been implicated in accounting for the diminished graft survival and therapeutic effect. To prove this assertion, we silenced the expression of NADPH subunits (p22-phox, p47-phox, and p67-phox) and small GTPase Rac1 in BMMSCs using shRNA. Our results showed that silencing these proteins significantly reduced oxidative stress and cell death/apoptosis, and promoted implanted BMMSCs proliferation after TBI. The most significant result was however seen with Rac1 silencing, which demonstrated decreased expression of apoptotic proteins, enhanced in vitro survival ratio, reduction in TBI lesional volume and significant improvement in neurological function post shRac1-BMMSCs transplantation. Additionally, two RNA-seq hub genes (VEGFA and MMP-2) were identified to play critical roles in shRac1-mediated cell survival. In summary, we propose that knockdown of Rac1 gene could significantly boost cell survival and promote the recovery of neurological functions after BMMSCs transplantation in TBI mice. Impact Journals 2020-12-19 /pmc/articles/PMC7880331/ /pubmed/33411679 http://dx.doi.org/10.18632/aging.202334 Text en Copyright: © 2020 Huang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Huang, Dongdong Siaw-Debrah, Felix Wang, Hua Ye, Sheng Wang, Kankai Wu, Ke Zhang, Ying Wang, Hao Yao, Chaojie Chen, Jiayu Yan, Lin Zhang, Chun-Li Zhuge, Qichuan Yang, Jianjing Transplanting Rac1-silenced bone marrow mesenchymal stem cells promote neurological function recovery in TBI mice |
title | Transplanting Rac1-silenced bone marrow mesenchymal stem cells promote neurological function recovery in TBI mice |
title_full | Transplanting Rac1-silenced bone marrow mesenchymal stem cells promote neurological function recovery in TBI mice |
title_fullStr | Transplanting Rac1-silenced bone marrow mesenchymal stem cells promote neurological function recovery in TBI mice |
title_full_unstemmed | Transplanting Rac1-silenced bone marrow mesenchymal stem cells promote neurological function recovery in TBI mice |
title_short | Transplanting Rac1-silenced bone marrow mesenchymal stem cells promote neurological function recovery in TBI mice |
title_sort | transplanting rac1-silenced bone marrow mesenchymal stem cells promote neurological function recovery in tbi mice |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880331/ https://www.ncbi.nlm.nih.gov/pubmed/33411679 http://dx.doi.org/10.18632/aging.202334 |
work_keys_str_mv | AT huangdongdong transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice AT siawdebrahfelix transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice AT wanghua transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice AT yesheng transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice AT wangkankai transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice AT wuke transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice AT zhangying transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice AT wanghao transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice AT yaochaojie transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice AT chenjiayu transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice AT yanlin transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice AT zhangchunli transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice AT zhugeqichuan transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice AT yangjianjing transplantingrac1silencedbonemarrowmesenchymalstemcellspromoteneurologicalfunctionrecoveryintbimice |