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.
Authors
- Chun‐Li Zhang (ORCID: https://orcid.org/0000-0002-2639-4605)
- Sergio Cananzi (ORCID: https://orcid.org/0000-0001-6090-9652)
- Leilei Wang (ORCID: https://orcid.org/0000-0002-3559-043X)
- Tianjin Shen
- Carolina Serrano
Institutions
- The University of Texas Southwestern Medical Center (US)
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
Funders
- Texas Alzheimer's Research and Care Consortium
- National Institutes of Health
- University of Texas Health Science Center at San Antonio