Simple and Highly Specific Targeting of Resident Microglia with Adeno-Associated Virus.
Carolina SerranoSergio CananziTianjin ShenLei-Lei WangChun-Li ZhangPublished in: bioRxiv : the preprint server for biology (2023)
Microglia, as the immune cells of the central nervous system (CNS), play dynamic roles in both health 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 IBA1 ( hIBA1 ) promoter. This targeting approach is applicable to both resting and reactive microglia. When combining the short hIBA1 promoter with the target sequence of miR124, up to 95% of transduced cells are identified as microglia. Such a simple and highly specific microglia-targeting strategy may be further optimized for research and therapeutics.
Keyphrases
- inflammatory response
- neuropathic pain
- cancer therapy
- cell proliferation
- gene therapy
- endothelial cells
- dna methylation
- healthcare
- gene expression
- small molecule
- spinal cord injury
- transcription factor
- induced apoptosis
- spinal cord
- blood brain barrier
- risk assessment
- heart rate
- cell free
- heart rate variability
- cerebrospinal fluid