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Intravenous rAAV9 Produces Time-Resolved Parenchymal Labeling Downstream of the Vasculature in Adult Mice

  • Alejandro Soto-Avellaneda
  • , Anton D. Pugel
  • , Jocelyn R. Holmes
  • , Alyssa M. Hicks
  • , Sara Z. Alsaifi
  • , Gyandarshika Koirala
  • , Alexandra E. Oxford
  • , Brad E. Morrison
  • Boise State University

Research output: Contribution to journalArticlepeer-review

Abstract

Intravenous delivery of recombinant adeno-associated virus serotype 9 can lead to reporter activation in cell types beyond the vasculature, but the routes enabling downstream parenchymal labeling remain unclear. Here, we provide a systematic, time-resolved map of parenchymal labeling after a single intravenous dose of rAAV9 encoding Cre recombinase under a ubiquitous promoter in healthy adult Ai9 reporter mice. Following retro-orbital administration, we quantified tdTomato-positive labeling across 25 targets at multiple time points over six months and observed durable reporter activation in several nonvascular parenchymal populations relevant to systemic gene-delivery applications. We also identify a set of parenchymal cell types that are consistently labeled in both this vascularly initiated reporter system and our prior adult VE-cadherin-driven reporter paradigm, supporting a connection to vascular exposure without asserting lineage relationships. These results nominate mechanistic routes for future disambiguation, including viral transcytosis across endothelium, endothelial cell transdifferentiation and extracellular-vesicle-mediated transfer. The dataset and methods provide a reference framework for investigators optimizing systemic delivery and interpreting downstream labeling in vivo.

Original languageEnglish
Article number421
JournalBiology
Volume15
Issue number5
DOIs
StatePublished - Mar 2026

Keywords

  • Ai9 reporter
  • CRE recombinase
  • biodistribution
  • intravenous delivery
  • parenchyma
  • recombinant AAV9
  • systemic gene delivery
  • tdTomato
  • vasculature

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