Thuringer Dominique, Solary Eric, Garrido Carmen
INSERM U1231, Université de Bourgogne Franche ComtéDijon, France.
INSERM U1170, Institut Gustave RoussyVillejuif, France.
Front Mol Neurosci. 2017 Aug 4;10:246. doi: 10.3389/fnmol.2017.00246. eCollection 2017.
Brain microvascular endothelial cells (BMECs) separate the peripheral blood from the brain. These cells, which are surrounded by basal lamina, pericytes and glial cells, are highly interconnected through tight and gap junctions. Their permeability properties restrict the transfer of potentially useful therapeutic agents. In such a hermetic system, the gap junctional exchange of small molecules between cerebral endothelial and non-endothelial cells is crucial for maintaining tissue homeostasis. MicroRNA were shown to cross gap junction channels, thereby modulating gene expression and function of the recipient cell. It was also shown that, when altered, BMEC could be regenerated by endothelial cells derived from pluripotent stem cells. Here, we discuss the transfer of microRNA through gap junctions between BMEC, the regeneration of BMEC from induced pluripotent stem cells that could be engineered to express specific microRNA, and how such an innovative approach could benefit to the treatment of glioblastoma and other neurological diseases.
脑微血管内皮细胞(BMECs)将外周血与脑分隔开来。这些细胞被基膜、周细胞和神经胶质细胞所包围,通过紧密连接和缝隙连接高度相互连接。它们的通透性特性限制了潜在有用治疗剂的转运。在这样一个封闭系统中,脑内皮细胞与非内皮细胞之间小分子的缝隙连接交换对于维持组织内环境稳定至关重要。已表明微小RNA可穿过缝隙连接通道,从而调节受体细胞的基因表达和功能。还表明,当BMEC发生改变时,可由多能干细胞衍生的内皮细胞使其再生。在此,我们讨论微小RNA通过BMEC之间的缝隙连接的转运、可被工程化以表达特定微小RNA的诱导多能干细胞对BMEC的再生,以及这种创新方法如何有益于胶质母细胞瘤和其他神经疾病的治疗。