Ultramicroscopy as a novel tool to unravel the tropism of AAV gene therapy vectors in the brain

• Verfasst von: Alves, Sandro [VerfasserIn]
• Verfasst von: Kalle, Christof von [VerfasserIn]
• Titel: Ultramicroscopy as a novel tool to unravel the tropism of AAV gene therapy vectors in the brain
• Verf.angabe: Sandro Alves, Julia Bode, Alexis-Pierre Bemelmans, Christof von Kalle, Nathalie Cartier and Björn Tews
• E-Jahr: 2016
• Jahr: 20 June 2016
• Umfang: 12 S.
• Fussnoten: Gesehen am 11.12.2018
• Titel Quelle: Enthalten in: Scientific reports
• Ort Quelle: [London] : Macmillan Publishers Limited, part of Springer Nature, 2011
• Jahr Quelle: 2016
• Band/Heft Quelle: 6(2016), Artikel-ID 28272
• ISSN Quelle: 2045-2322
• DOI: doi:10.1038/srep28272
• Datenträger: Online-Ressource
• Sprache: eng
• K10plus-PPN: 1585086290

Abstract

Recombinant adeno-associated viral (AAV) vectors have advanced to the vanguard of gene therapy. Numerous naturally occurring serotypes have been used to target cells in various tissues. There is a strong need for fast and dynamic methods which efficiently unravel viral tropism in whole organs. Ultramicroscopy (UM) is a novel fluorescence microscopy technique that images optically cleared undissected specimens, achieving good resolutions at high penetration depths while being non-destructive. UM was applied to obtain high-resolution 3D analysis of AAV transduction in adult mouse brains, especially in the hippocampus, a region of interest for Alzheimer’s disease therapy. We separately or simultaneously compared transduction efficacies for commonly used serotypes (AAV9 and AAVrh10) using fluorescent reporter expression. We provide a detailed comparative and quantitative analysis of the transduction profiles. UM allowed a rapid analysis of marker fluorescence expression in neurons with intact projections deep inside the brain, in defined anatomical structures. Major hippocampal neuronal transduction was observed with both vectors, with slightly better efficacy for AAV9 in UM. Glial response and synaptic marker expression did not change post transduction.We propose UM as a novel valuable complementary tool to efficiently and simultaneously unravel tropism of different viruses in a single non-dissected adult rodent brain.