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Noninvasive focal transgene delivery with viral neuronal tracers in the marmoset monkey.
Parks, T Vincenza; Szczupak, Diego; Choi, Sang-Ho; Schaeffer, David J.
Affiliation
  • Parks TV; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Szczupak D; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Choi SH; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Schaeffer DJ; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA. Electronic address: dschaeff@pitt.edu.
Cell Rep Methods ; 4(2): 100709, 2024 Feb 26.
Article in En | MEDLINE | ID: mdl-38359822
ABSTRACT
We establish a reliable method for selectively delivering adeno-associated viral vectors (AAVs) across the blood-brain barrier (BBB) in the marmoset without the need for neurosurgical injection. We focally perturbed the BBB (∼1 × 2 mm) in area 8aD of the frontal cortex in four adult marmoset monkeys using low-intensity transcranial focused ultrasound aided by microbubbles. Within an hour of opening the BBB, either AAV2 or AAV9 was delivered systemically via tail-vein injection. In all four marmosets, fluorescence-encoded neurons were observed at the site of BBB perturbation, with AAV2 showing a sparse distribution of transduced neurons when compared to AAV9. The results are compared to direct intracortical injections of anterograde tracers into area 8aD and similar (albeit sparser) long-range connectivity was observed. With evidence of transduced neurons specific to the region of BBB opening as well as long-distance tracing, we establish a framework for focal noninvasive transgene delivery to the marmoset brain.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain / Callithrix Limits: Animals Language: En Journal: Cell Rep Methods Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain / Callithrix Limits: Animals Language: En Journal: Cell Rep Methods Year: 2024 Document type: Article Affiliation country: Country of publication: