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Gap junction-mediated cell-cell interaction between transplanted mesenchymal stem cells and vascular endothelium in stroke.
Kikuchi-Taura, Akie; Okinaka, Yuka; Saino, Orie; Takeuchi, Yukiko; Ogawa, Yuko; Kimura, Takafumi; Gul, Sheraz; Claussen, Carsten; Boltze, Johannes; Taguchi, Akihiko.
  • Kikuchi-Taura A; Department of Regenerative Medicine Research, Foundation for Biomedical Research and Innovation at Kobe, Hyogo, Japan.
  • Okinaka Y; Department of Regenerative Medicine Research, Foundation for Biomedical Research and Innovation at Kobe, Hyogo, Japan.
  • Saino O; Department of Regenerative Medicine Research, Foundation for Biomedical Research and Innovation at Kobe, Hyogo, Japan.
  • Takeuchi Y; Department of Regenerative Medicine Research, Foundation for Biomedical Research and Innovation at Kobe, Hyogo, Japan.
  • Ogawa Y; Department of Regenerative Medicine Research, Foundation for Biomedical Research and Innovation at Kobe, Hyogo, Japan.
  • Kimura T; Japanese Red Cross Kinki Block Blood Center, Osaka, Japan.
  • Gul S; Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Hamburg, Germany.
  • Claussen C; Fraunhofer Cluster of Excellence for Immune-Mediated Diseases CIMD, Hamburg, Germany.
  • Boltze J; Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Hamburg, Germany.
  • Taguchi A; Fraunhofer Cluster of Excellence for Immune-Mediated Diseases CIMD, Hamburg, Germany.
Stem Cells ; 39(7): 904-912, 2021 07.
Article in English | MEDLINE | ID: covidwho-1126519
ABSTRACT
We have shown previously that transplanted bone marrow mononuclear cells (BM-MNC), which are a cell fraction rich in hematopoietic stem cells, can activate cerebral endothelial cells via gap junction-mediated cell-cell interaction. In the present study, we investigated such cell-cell interaction between mesenchymal stem cells (MSC) and cerebral endothelial cells. In contrast to BM-MNC, for MSC we observed suppression of vascular endothelial growth factor uptake into endothelial cells and transfer of glucose from endothelial cells to MSC in vitro. The transfer of such a small molecule from MSC to vascular endothelium was subsequently confirmed in vivo and was followed by suppressed activation of macrophage/microglia in stroke mice. The suppressive effect was absent by blockade of gap junction at MSC. Furthermore, gap junction-mediated cell-cell interaction was observed between circulating white blood cells and MSC. Our findings indicate that gap junction-mediated cell-cell interaction is one of the major pathways for MSC-mediated suppression of inflammation in the brain following stroke and provides a novel strategy to maintain the blood-brain barrier in injured brain. Furthermore, our current results have the potential to provide a novel insight for other ongoing clinical trials that make use of MSC transplantation aiming to suppress excess inflammation, as well as other diseases such as COVID-19 (coronavirus disease 2019).
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Cell Communication / Gap Junctions / Stroke / Mesenchymal Stem Cell Transplantation / Mesenchymal Stem Cells / Human Umbilical Vein Endothelial Cells Type of study: Prognostic study Limits: Animals / Humans Language: English Journal: Stem Cells Year: 2021 Document Type: Article Affiliation country: Stem.3360

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Cell Communication / Gap Junctions / Stroke / Mesenchymal Stem Cell Transplantation / Mesenchymal Stem Cells / Human Umbilical Vein Endothelial Cells Type of study: Prognostic study Limits: Animals / Humans Language: English Journal: Stem Cells Year: 2021 Document Type: Article Affiliation country: Stem.3360