Ultrasound-Mediated Blood-Brain Barrier Opening Improves Whole Brain Gene Delivery in Mice

Archive ouverte

Felix, Marie-Solenne | Borloz, Emilie | Metwally, Khaled | Dauba, Ambre | Larrat, Benoit | Matagne, Valerie | Ehinger, Yann | Villard, Laurent | Novell, Anthony | Mensah, Serge | Roux, Jean-Christophe

Edité par CCSD ; MDPI -

International audience. Gene therapy represents a powerful therapeutic tool to treat diseased tissues and provide a durable and effective correction. The central nervous system (CNS) is the target of many gene therapy protocols, but its high complexity makes it one of the most difficult organs to reach, in part due to the blood-brain barrier that protects it from external threats. Focused ultrasound (FUS) coupled with microbubbles appears as a technological breakthrough to deliver therapeutic agents into the CNS. While most studies focus on a specific targeted area of the brain, the present work proposes to permeabilize the entire brain for gene therapy in several pathologies. Our results show that, after i.v. administration and FUS sonication in a raster scan manner, a self-complementary AAV9-CMV-GFP vector strongly and safely infected the whole brain of mice. An increase in vector DNA (19.8 times), GFP mRNA (16.4 times), and GFP protein levels (17.4 times) was measured in whole brain extracts of FUS-treated GFP injected mice compared to non-FUS GFP injected mice. In addition to this increase in GFP levels, on average, a 7.3-fold increase of infected cells in the cortex, hippocampus, and striatum was observed. No side effects were detected in the brain of treated mice. The combining of FUS and AAV-based gene delivery represents a significant improvement in the treatment of neurological genetic diseases.

Suggestions

Du même auteur

Ultrasound-induced seizures in a mouse model of KCNQ2-NEO-DEE

Archive ouverte | Brun, Lucile | CCSD

International audience

State‐of‐the‐art therapies for Rett syndrome

Archive ouverte | Panayotis, Nicolas | CCSD

International audience. Rett syndrome (RTT) is an X-linked neurogenetic disorder caused by mutations of the MECP2 (methyl-CpG-binding protein 2) gene. Over two decades of work established MeCP2 as a protein with piv...

A new method to assess weight-bearing distribution after central nervous system lesions in rats

Archive ouverte | Pertici, Vincent | CCSD

International audience. The aim of the present study is to assess the relevance of weight-bearing distribution (DWB) measurement in freely moving rats after stroke and thoracic spinal cord injuries. Animals were div...

Chargement des enrichissements...