Robo4 inhibits gamma radiation-induced permeability of a murine microvascular endothelial cell by regulating the junctions

Cellular & Molecular Biology Letters

Research Letter

Alhaji Osman Smith¹  Yizhou Wang¹  Lingyu Zeng¹  Haiyang Wang¹  Kailin Xu¹  Jianlin Qiao¹  Yue Li¹  Yuwei Du¹  Yurong Bao¹  Guozhang Wang²  Seyram Yao Adzraku²  Wen Ju²  Can Cao² 

[1]Blood Diseases Institute, Xuzhou Medical University, 221002, Xuzhou, China

[2]Key Laboratory of Bone Marrow Stem Cell, 221002, Xuzhou, Jiangsu, China

[3]Department of Hematology, The Affiliated Hospital of Xuzhou Medical University, 221002, Xuzhou, China

[4]Blood Diseases Institute, Xuzhou Medical University, 221002, Xuzhou, China

[5]Key Laboratory of Bone Marrow Stem Cell, 221002, Xuzhou, Jiangsu, China

[6]Department of Hematology, The Affiliated Hospital of Xuzhou Medical University, 221002, Xuzhou, China

[7]Xuzhou Ruihu Health Management Consulting Co., Ltd, 221002, Xuzhou, China

关键词: Robo4;    Microvascular endothelial cells;    Endothelial junctions;    Irradiation;    Permeability;   

DOI  :  10.1186/s11658-022-00413-w

 received in 2022-09-09, accepted in 2022-12-19,  发布年份 2022

来源: Springer

【 摘 要 】

BackgroundHematopoietic stem cell transplantation involves irradiation preconditioning which causes bone marrow endothelial cell dysfunction. While much emphasis is on the reconstitution of hematopoietic stem cells in the bone marrow microenvironment, endothelial cell preservation is indispensable to overcome the preconditioning damages. This study aims to ascertain the role of Roundabout 4 (Robo4) in regulating irradiation-induced damage to the endothelium.MethodsMicrovascular endothelial cells were treated with γ-radiation to establish an endothelial cell injury model. Robo4 expression in the endothelial cells was manipulated employing lentiviral-mediated RNAi and gene overexpression technology before irradiation treatment. The permeability of endothelial cells was measured using qPCR, immunocytochemistry, and immunoblotting to analyze the effect on the expression and distribution of junctional molecules, adherens junctions, tight junctions, and gap junctions. Using Transwell endothelial monolayer staining, FITC-Dextran permeability, and gap junction-mediated intercellular communication (GJIC) assays, we determined the changes in endothelial functions after Robo4 gene manipulation and irradiation. Moreover, we measured the proportion of CD31 expression in endothelial cells by flow cytometry. We analyzed variations between two or multiple groups using Student’s t-tests and ANOVA.ResultsIonizing radiation upregulates Robo4 expression but disrupts endothelial junctional molecules. Robo4 deletion causes further degradation of endothelial junctions hence increasing the permeability of the endothelial cell monolayer. Robo4 knockdown in microvascular endothelial cells increases the degradation and delocalization of ZO-1, PECAM-1, occludin, and claudin-5 molecules after irradiation. Conversely, connexin 43 expression increases after silencing Robo4 in endothelial cells to induce permeability but are readily destroyed when exposed to 10 Gy of gamma radiation. Also, Robo4 knockdown enhances Y731-VE-cadherin phosphorylation leading to the depletion and destabilization of VE-cadherin at the endothelial junctions following irradiation. However, Robo4 overexpression mitigates irradiation-induced degradation of tight junctional proteins and stabilizes claudin-5 and ZO-1 distribution. Finally, the enhanced expression of Robo4 ameliorates the irradiation-induced depletion of VE-cadherin and connexin 43, improves the integrity of microvascular endothelial cell junctions, and decreases permeability.ConclusionThis study reveals that Robo4 maintains microvascular integrity after radiation preconditioning treatment by regulating endothelial permeability and protecting endothelial functions. Our results also provided a potential mechanism to repair the bone marrow vascular niche after irradiation by modulating Robo4 expression.

【 授权许可】

CC BY   
© The Author(s) 2023

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