Simple and highly specific targeting of resident microglia with adeno-associated virus

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 <i>IBA1</i> (<i>hIBA1</i>) promoter. This targeting approach is applicable to both resting and reactive microglia. When combining the short <i>hIBA1</i> promoter with the target sequence of <i>miR124</i>, 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.

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Publication Details

Journal
iScience
Published
2024-08-12
DOI
https://doi.org/10.1016/j.isci.2024.110706
Citations
17
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
4.21

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Simple and highly specific targeting of resident microglia with adeno-associated virus

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article

Simple and highly specific targeting of resident microglia with adeno-associated virus

Chun‐Li Zhang, Sergio Cananzi, Leilei Wang, Tianjin Shen, Carolina Serrano
article en
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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 <i>IBA1</i> (<i>hIBA1</i>) promoter. This targeting approach is applicable to both resting and reactive microglia. When combining the short <i>hIBA1</i> promoter with the target sequence of <i>miR124</i>, 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.

iScienceVol. 27(9)
The University of Texas Southwestern Medical Center (US)
Texas Alzheimer's Research and Care Consortium, National Institutes of Health, University of Texas Health Science Center at San Antonio
Openalex Percentile: Top 5%
Neuroinflammation and Neurodegeneration Mechanisms
4.21
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