Constitutive Expression of Adiponectin in Endothelial Progenitor Cells Protects a Rat Model of Cerebral Ischemia
Endothelial progenitor cells (EPCs), as precursors to endothelial cells, play a significant part in the process of endogenous blood vessel repair and maintenance of endothelial integrity. Adiponectin (APN) is an adipocyte-specific adipocytokine. In this study, we aim to test whether we transplant a...
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Published in | Journal of neural transplantation & plasticity Vol. 2017; no. 2017; pp. 1 - 8 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cairo, Egypt
Hindawi Publishing Corporation
01.01.2017
Hindawi John Wiley & Sons, Inc Wiley |
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Abstract | Endothelial progenitor cells (EPCs), as precursors to endothelial cells, play a significant part in the process of endogenous blood vessel repair and maintenance of endothelial integrity. Adiponectin (APN) is an adipocyte-specific adipocytokine. In this study, we aim to test whether we transplant a combined graft of EPCs transfected with the adiponectin gene into a rat model of cerebral ischemia could improve functional recovery after middle cerebral artery occlusion (MCAO). Sprague-Dawley (SD) rats were randomly divided into a MCAO control group, a MCAO EPC treatment group, and a MCAO LV-APN-EPC treatment group. A focal cerebral ischemia and reperfusion model was induced by the intraluminal suture method. After 2 h of reperfusion, EPCs were transplanted by injection through the tail vein. A rotarod test was conducted to assess behavioral function before MCAO and on days 1, 7, and 14 after MCAO. After 14 d, TTC staining, CD31 immunofluorescence, and TUNEL staining were used to evaluate infarct volume, microvessel density, and cell apoptosis. Results revealed that behavioral function, infarct area percentage, microvessel density, and cell apoptosis rates were more favorable in the LV-APN-EPC treatment group than in the EPC treatment group. These data suggested that gene-modified cell therapy may be a useful approach for the treatment of ischemic stroke. |
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AbstractList | Endothelial progenitor cells (EPCs), as precursors to endothelial cells, play a significant part in the process of endogenous blood vessel repair and maintenance of endothelial integrity. Adiponectin (APN) is an adipocyte-specific adipocytokine. In this study, we aim to test whether we transplant a combined graft of EPCs transfected with the adiponectin gene into a rat model of cerebral ischemia could improve functional recovery after middle cerebral artery occlusion (MCAO). Sprague-Dawley (SD) rats were randomly divided into a MCAO control group, a MCAO EPC treatment group, and a MCAO LV-APN-EPC treatment group. A focal cerebral ischemia and reperfusion model was induced by the intraluminal suture method. After 2 h of reperfusion, EPCs were transplanted by injection through the tail vein. A rotarod test was conducted to assess behavioral function before MCAO and on days 1, 7, and 14 after MCAO. After 14 d, TTC staining, CD31 immunofluorescence, and TUNEL staining were used to evaluate infarct volume, microvessel density, and cell apoptosis. Results revealed that behavioral function, infarct area percentage, microvessel density, and cell apoptosis rates were more favorable in the LV-APN-EPC treatment group than in the EPC treatment group. These data suggested that gene-modified cell therapy may be a useful approach for the treatment of ischemic stroke. Endothelial progenitor cells (EPCs), as precursors to endothelial cells, play a significant part in the process of endogenous blood vessel repair and maintenance of endothelial integrity. Adiponectin (APN) is an adipocyte-specific adipocytokine. In this study, we aim to test whether we transplant a combined graft of EPCs transfected with the adiponectin gene into a rat model of cerebral ischemia could improve functional recovery after middle cerebral artery occlusion (MCAO). Sprague-Dawley (SD) rats were randomly divided into a MCAO control group, a MCAO EPC treatment group, and a MCAO LV-APN-EPC treatment group. A focal cerebral ischemia and reperfusion model was induced by the intraluminal suture method. After 2 h of reperfusion, EPCs were transplanted by injection through the tail vein. A rotarod test was conducted to assess behavioral function before MCAO and on days 1, 7, and 14 after MCAO. After 14 d, TTC staining, CD31 immunofluorescence, and TUNEL staining were used to evaluate infarct volume, microvessel density, and cell apoptosis. Results revealed that behavioral function, infarct area percentage, microvessel density, and cell apoptosis rates were more favorable in the LV-APN-EPC treatment group than in the EPC treatment group. These data suggested that gene-modified cell therapy may be a useful approach for the treatment of ischemic stroke.Endothelial progenitor cells (EPCs), as precursors to endothelial cells, play a significant part in the process of endogenous blood vessel repair and maintenance of endothelial integrity. Adiponectin (APN) is an adipocyte-specific adipocytokine. In this study, we aim to test whether we transplant a combined graft of EPCs transfected with the adiponectin gene into a rat model of cerebral ischemia could improve functional recovery after middle cerebral artery occlusion (MCAO). Sprague-Dawley (SD) rats were randomly divided into a MCAO control group, a MCAO EPC treatment group, and a MCAO LV-APN-EPC treatment group. A focal cerebral ischemia and reperfusion model was induced by the intraluminal suture method. After 2 h of reperfusion, EPCs were transplanted by injection through the tail vein. A rotarod test was conducted to assess behavioral function before MCAO and on days 1, 7, and 14 after MCAO. After 14 d, TTC staining, CD31 immunofluorescence, and TUNEL staining were used to evaluate infarct volume, microvessel density, and cell apoptosis. Results revealed that behavioral function, infarct area percentage, microvessel density, and cell apoptosis rates were more favorable in the LV-APN-EPC treatment group than in the EPC treatment group. These data suggested that gene-modified cell therapy may be a useful approach for the treatment of ischemic stroke. |
Audience | Academic |
Author | Yu, Qing Wang, Meiyao Xie, Xiaorui Zhang, Renwei Li, Yan Liu, Yumin Feng, Hongliang |
AuthorAffiliation | 2 Department of Neurology, Xiangyang Central Hospital, Xiangyang 441000, China 1 Department of Neurology, Zhongnan Hospital of Wuhan University, Wuhan 430071, China |
AuthorAffiliation_xml | – name: 2 Department of Neurology, Xiangyang Central Hospital, Xiangyang 441000, China – name: 1 Department of Neurology, Zhongnan Hospital of Wuhan University, Wuhan 430071, China |
Author_xml | – sequence: 1 fullname: Liu, Yumin – sequence: 2 fullname: Wang, Meiyao – sequence: 3 fullname: Feng, Hongliang – sequence: 4 fullname: Yu, Qing – sequence: 5 fullname: Xie, Xiaorui – sequence: 6 fullname: Zhang, Renwei – sequence: 7 fullname: Li, Yan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29201467$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1152_ajpcell_00200_2018 crossref_primary_10_2174_1574888X15666200331135227 crossref_primary_10_3390_biomedicines10102616 crossref_primary_10_1155_2020_1273198 crossref_primary_10_3389_fneur_2021_630681 crossref_primary_10_31744_einstein_journal_2020RW5160 |
Cites_doi | 10.2337/db16-er10b 10.1126/science.275.5302.964 10.1016/j.jneumeth.2008.06.018 10.1016/s0022-510x(00)00268-9 10.1371/journal.pone.0136819 10.1161/STR.0000000000000024 10.1371/journal.pone.0050105 10.1038/ajh.2008.278 10.1016/j.pneurobio.2007.08.001 10.1016/j.febslet.2009.07.011 10.1038/7434 10.1161/01.cir.103.5.634 10.1038/jcbfm.1990.47 10.1074/jbc.270.45.26746 10.1161/01.HYP.0000168923.92885.f7 10.2337/diabetes.53.1.195 10.2174/138161212799859657 10.1002/stem.219 10.1016/j.jvs.2009.05.049 10.1161/hh0302.104460 10.1038/386671a0 10.1161/01.RES.0000268193.46418.d1 10.1016/j.yjmcc.2011.03.008 10.1056/NEJMoa070240 10.1161/01.cir.0000039526.42991.93 10.12659/MSM.892299 10.1056/nejmc060685 10.1002/ana.21919 10.1074/jbc.M310389200 10.1161/01.str.20.1.84 |
ContentType | Journal Article |
Copyright | Copyright © 2017 Renwei Zhang et al. COPYRIGHT 2017 John Wiley & Sons, Inc. Copyright © 2017 Renwei Zhang et al. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Copyright © 2017 Renwei Zhang et al. 2017 |
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Snippet | Endothelial progenitor cells (EPCs), as precursors to endothelial cells, play a significant part in the process of endogenous blood vessel repair and... |
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SubjectTerms | Antibodies Bone marrow Carotid arteries Cerebral ischemia Endothelium Experiments Ischemia Laboratory animals Peptide hormones Physiological aspects Proteins Stroke Veins & arteries |
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Title | Constitutive Expression of Adiponectin in Endothelial Progenitor Cells Protects a Rat Model of Cerebral Ischemia |
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