» Articles » PMID: 39297168

Simple and Highly Specific Targeting of Resident Microglia with Adeno-associated Virus

Overview
Journal iScience
Publisher Cell Press
Date 2024 Sep 19
PMID 39297168
Authors
Affiliations
Soon will be listed here.
Abstract

Microglia, as the immune cells of the central nervous system (CNS), play dynamic roles in both healthy and diseased conditions. The ability to genetically target microglia using viruses is crucial for understanding their functions and advancing microglia-based treatments. We here show that resident microglia can be simply and specifically targeted using adeno-associated virus (AAV) vectors containing a 466-bp DNA fragment from the human () promoter. This targeting approach is applicable to both resting and reactive microglia. When combining the short promoter with the target sequence of , up to 98% of transduced cells are identified as microglia. Such a simple and highly specific microglia-targeting strategy may be further optimized for research and therapeutics.

Citing Articles

Expression-based selection identifies a microglia-tropic AAV capsid for direct and CSF routes of administration in mice.

Santoscoy M, Espinoza P, Hanlon K, Yang L, Nieland L, Ng C bioRxiv. 2024; .

PMID: 39386560 PMC: 11463440. DOI: 10.1101/2024.09.25.614546.

References
1.
OCarroll S, Cook W, Young D . AAV Targeting of Glial Cell Types in the Central and Peripheral Nervous System and Relevance to Human Gene Therapy. Front Mol Neurosci. 2021; 13:618020. PMC: 7829478. DOI: 10.3389/fnmol.2020.618020. View

2.
Wu Y, Dissing-Olesen L, MacVicar B, Stevens B . Microglia: Dynamic Mediators of Synapse Development and Plasticity. Trends Immunol. 2015; 36(10):605-613. PMC: 4841266. DOI: 10.1016/j.it.2015.08.008. View

3.
Aschauer D, Kreuz S, Rumpel S . Analysis of transduction efficiency, tropism and axonal transport of AAV serotypes 1, 2, 5, 6, 8 and 9 in the mouse brain. PLoS One. 2013; 8(9):e76310. PMC: 3785459. DOI: 10.1371/journal.pone.0076310. View

4.
Cronin J, Zhang X, Reiser J . Altering the tropism of lentiviral vectors through pseudotyping. Curr Gene Ther. 2005; 5(4):387-98. PMC: 1368960. DOI: 10.2174/1566523054546224. View

5.
Tai W, Zhang C . In vivo cell fate reprogramming for spinal cord repair. Curr Opin Genet Dev. 2023; 82:102090. PMC: 11025462. DOI: 10.1016/j.gde.2023.102090. View