Aryal Muna, Fischer Krisztina, Gentile Caroline, Gitto Salvatore, Zhang Yong-Zhi, McDannold Nathan
Department of Radiology, Brigham & Women's Hospital, Harvard Medical School, Boston, United States of America.
Department of Neurobiology, Harvard College, Cambridge, United States of America.
PLoS One. 2017 Jan 3;12(1):e0166061. doi: 10.1371/journal.pone.0166061. eCollection 2017.
Many blood-borne substances attempting to pass through the luminal membrane of brain endothelial cells are acted upon by a variety of metabolizing enzymes or are actively expelled back into the capillary lumen by embedded efflux transporters, such as Permeability-glycoprotein (Pgp). Overexpression of this protein has also been linked to multidrug resistance in cancer cells. Previous studies have shown that focused ultrasound (FUS), when combined with a microbubble agent, has ability to temporarily disrupt blood-brain barrier (BBBD). In this work, we investigated whether modulation of Pgp expression is part of the FUS-induced effects. We found that ultrasound can temporarily suppress Pgp expression. When BBBD was produced at 0.55 MPa, Pgp was suppressed up to 48 hours and restored by 72 hours. At 0.81 MPa, suppression can last 72 hours or longer. These findings support the idea that microbubble-enhanced FUS disrupts the functional components of the BBB through suppression of drug efflux.
许多试图穿过脑内皮细胞腔面膜的血源物质会受到多种代谢酶的作用,或者被嵌入的外排转运蛋白(如通透糖蛋白,Pgp)主动排回毛细血管腔。这种蛋白的过表达也与癌细胞的多药耐药性有关。先前的研究表明,聚焦超声(FUS)与微泡剂联合使用时,有能力暂时破坏血脑屏障(BBBD)。在这项工作中,我们研究了Pgp表达的调节是否是FUS诱导效应的一部分。我们发现超声可以暂时抑制Pgp表达。当在0.55兆帕产生BBBD时,Pgp被抑制长达48小时,并在72小时恢复。在0.81兆帕时,抑制可持续72小时或更长时间。这些发现支持了微泡增强FUS通过抑制药物外排来破坏血脑屏障功能成分的观点。