Ginsenoside CK cooperates with bone mesenchymal stem cells to enhance angiogenesis post‐stroke via GLUT1 and HIF‐1α/VEGF pathway

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Hauptverfasser: Xijun Chen, Wenqi Qian, Ying Zhang, Peiqi Zhao, Xiangxiang Lin, Su Yang, Qichuan Zhuge, Haoqi Ni
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Veröffentlicht: Wiley 2024
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author Xijun Chen
Wenqi Qian
Ying Zhang
Peiqi Zhao
Xiangxiang Lin
Su Yang
Qichuan Zhuge
Haoqi Ni
author_facet Xijun Chen
Wenqi Qian
Ying Zhang
Peiqi Zhao
Xiangxiang Lin
Su Yang
Qichuan Zhuge
Haoqi Ni
Xijun Chen
Wenqi Qian
Ying Zhang
Peiqi Zhao
Xiangxiang Lin
Su Yang
Qichuan Zhuge
Haoqi Ni
collection Wiley Open Access
contents Ginsenoside CK cooperates with bone mesenchymal stem cells to enhance angiogenesis post‐stroke via GLUT1 and HIF‐1α/VEGF pathway Xijun Chen Wenqi Qian Ying Zhang Peiqi Zhao Xiangxiang Lin Su Yang Qichuan Zhuge Haoqi Ni Phytotherapy Research AbstractThe transplantation of bone marrow mesenchymal stem cells (MSCs) in stroke is hindered by the restricted rates of survival and differentiation. Ginsenoside compound K (CK), is reported to have a neuroprotective effect and regulate energy metabolism. We applied CK to investigate if CK could promote the survival of MSCs and differentiation into brain microvascular endothelial‐like cells (BMECs), thereby alleviating stroke symptoms. Therefore, transwell and middle cerebral artery occlusion (MCAO) models were used to mimic oxygen and glucose deprivation (OGD) in vitro and in vivo, respectively. Our results demonstrated that CK had a good affinity for GLUT1, which increased the expression of GLUT1 and the production of ATP, facilitated the proliferation and migration of MSCs, and activated the HIF‐1α/VEGF signaling pathway to promote MSC differentiation. Moreover, CK cooperated with MSCs to protect BMECs, promote angiogenesis and vascular density, enhance neuronal and astrocytic proliferation, thereby reducing infarct volume and consequently improving neurobehavioral outcomes. These results suggest that the synergistic effects of CK and MSCs could potentially be a promising strategy for stroke. 10.1002/ptr.8235 http://onlinelibrary.wiley.com/termsAndConditions#vor
doi_str_mv 10.1002/ptr.8235
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institution Wiley Open Access
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publishDate 2024
publisher Wiley
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spellingShingle Ginsenoside CK cooperates with bone mesenchymal stem cells to enhance angiogenesis post‐stroke via GLUT1 and HIF‐1α/VEGF pathway
Xijun Chen
Wenqi Qian
Ying Zhang
Peiqi Zhao
Xiangxiang Lin
Su Yang
Qichuan Zhuge
Haoqi Ni
Phytotherapy Research
Ginsenoside CK cooperates with bone mesenchymal stem cells to enhance angiogenesis post‐stroke via GLUT1 and HIF‐1α/VEGF pathway Xijun Chen Wenqi Qian Ying Zhang Peiqi Zhao Xiangxiang Lin Su Yang Qichuan Zhuge Haoqi Ni Phytotherapy Research AbstractThe transplantation of bone marrow mesenchymal stem cells (MSCs) in stroke is hindered by the restricted rates of survival and differentiation. Ginsenoside compound K (CK), is reported to have a neuroprotective effect and regulate energy metabolism. We applied CK to investigate if CK could promote the survival of MSCs and differentiation into brain microvascular endothelial‐like cells (BMECs), thereby alleviating stroke symptoms. Therefore, transwell and middle cerebral artery occlusion (MCAO) models were used to mimic oxygen and glucose deprivation (OGD) in vitro and in vivo, respectively. Our results demonstrated that CK had a good affinity for GLUT1, which increased the expression of GLUT1 and the production of ATP, facilitated the proliferation and migration of MSCs, and activated the HIF‐1α/VEGF signaling pathway to promote MSC differentiation. Moreover, CK cooperated with MSCs to protect BMECs, promote angiogenesis and vascular density, enhance neuronal and astrocytic proliferation, thereby reducing infarct volume and consequently improving neurobehavioral outcomes. These results suggest that the synergistic effects of CK and MSCs could potentially be a promising strategy for stroke. 10.1002/ptr.8235 http://onlinelibrary.wiley.com/termsAndConditions#vor
title Ginsenoside CK cooperates with bone mesenchymal stem cells to enhance angiogenesis post‐stroke via GLUT1 and HIF‐1α/VEGF pathway
topic Phytotherapy Research
url https://onlinelibrary.wiley.com/doi/10.1002/ptr.8235