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Targeting microglia with lentivirus and AAV: Recent advances and remaining challenges
Margaret E Maes1, Gloria Colombo1, Rouven Schulz1
1Institute of Science and Technology (IST) Austria, Am Campus 1, 3400 Klosterneuburg, Austria.
Abstract:
Microglia have emerged as a critical component of neurodegenerative diseases. Genetic manipulation of microglia can elucidate their functional impact in disease. In neuroscience, recombinant viruses such as lentiviruses and adeno-associated viruses (AAVs) have been successfully used to target various cell types in the brain, although effective transduction of microglia is rare. In this review, we provide a short background of lentiviruses and AAVs, and strategies for designing recombinant viral vectors. Then, we will summarize recent literature on successful microglial transductions in vitro and in vivo, and discuss the current challenges. Finally, we provide guidelines for reporting the efficiency and specificity of viral targeting in microglia, which will enable the microglial research community to assess and improve methodologies for future studies.
Insights
This review explores using viral vectors like lentiviruses and adeno-associated viruses (AAVs) for genetic manipulation of microglia, crucial cells in neurodegenerative diseases. It highlights challenges and offers guidelines for improving microglial transduction efficiency and specificity.
Area of Science:
- Neuroscience
- Immunology
- Genetics
Background:
- Microglia play a key role in neurodegenerative diseases.
- Genetic manipulation of microglia is essential for understanding their function.
- Current viral vector strategies for targeting brain cells, including microglia, face challenges in efficiency and specificity.
Purpose of the Study:
- To review the use of lentiviruses and adeno-associated viruses (AAVs) for microglial transduction.
- To summarize recent advancements and challenges in targeting microglia with viral vectors.
- To provide guidelines for reporting microglial transduction efficiency and specificity.
Main Methods:
- Review of existing literature on viral vector design and application in neuroscience.
- Analysis of studies reporting in vitro and in vivo microglial transduction.
- Development of reporting guidelines for microglial targeting methodologies.
Main Results:
- Lentiviruses and AAVs show potential for microglial gene delivery, but effective transduction remains challenging.
- Recent studies demonstrate progress in overcoming barriers to microglial targeting.
- There is a need for standardized reporting of transduction efficiency and specificity.
Conclusions:
- Optimizing viral vectors for microglial transduction is critical for advancing neurodegenerative disease research.
- Standardized reporting will facilitate the assessment and improvement of microglial targeting techniques.
- This review provides a framework for future research in microglial gene therapy and functional studies.
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