化学
可视化
四面体
DNA
细胞生物学
炸薯条
炎症
计算生物学
纳米技术
生物物理学
结晶学
生物
生物化学
内科学
数据挖掘
工程类
医学
材料科学
计算机科学
电气工程
作者
Yi Xu,Shuainan Li,Chenguang Wang,Xiaoming Xie,Xianqiang Mi
标识
DOI:10.1021/acs.analchem.3c01804
摘要
The blood-brain barrier (BBB) is essential for maintaining central nervous system (CNS) stability, and neuroinflammation may cause the dysfunction of the BBB. MicroRNA-146a (miR-146a) is closely associated with neuroinflammation, which showed significant upregulation in response to lipopolysaccharide (LPS) induction. Elucidating the relationship between LPS-induced miR-146a expression and the BBB could decipher the mechanism of many neurological diseases. Here, we constructed an in vitro microfluidic human-BBB (μF-hBBB) chip consisting of human umbilical vein vascular endothelial cells (HUVECs) and human astrocyte (HAs) cells. A tetrahedral DNA framework (TDF-3MB) nanoprobe was used to label miR-146a in HUVECs on μF-hBBB chips before and after LPS induction, and the study revealed a significant increase in miR-146a expression after LPS induction. We believe that such a μF-hBBB chip is a promising in vitro platform for further use in understanding CNS diseases.
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