Endogenous microRNA regulation suppresses transgene expression in hematopoietic lineages and enables stable gene transfer
Abstract
MicroRNAs (miRNAs) are small noncoding RNAs that regulate gene expression by repressing translation of target cellular transcripts. Increasing evidence indicates that miRNAs have distinct expression profiles and play crucial roles in numerous cellular processes, although the extent of miRNA regulation is not well known. By challenging mice with lentiviral vectors encoding target sequences of endogenous miRNAs, we show the efficiency of miRNAs in sharply segregating gene expression among different tissues. Transgene expression from vectors incorporating target sequences for mir-142-3p was effectively suppressed in intravascular and extravascular hematopoietic lineages, whereas expression was maintained in nonhematopoietic cells. This expression profile, which could not be attained until now, enabled stable gene transfer in immunocompetent mice, thus overcoming a major hurdle to successful gene therapy. Our results provide novel in situ evidence of miRNA regulation and demonstrate a new paradigm in vector design with applications for genetic engineering and therapeutic gene transfer.
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Four tandem complementary copies of the hematopoietic-specific miR-142-3p sequence inserted downstream of a GFP reporter significantly prevented transgene expression in hematopoietic cells, even after superinfection with 30 copies of viruses.
“For example, four tandem complimentary copies of the hematopoietic-specific miR-142-3p sequence were inserted into the downstream of a green fluorescent protein (GFP) reporter. It significantly prevented transgene expression in hematopoietic cells, even after the cells were superinfected with 30 copies of viruses [31].”
From Designing and optimizing AAV-mediated gene therapy for neurodegenerative diseases: from bench to bedside (2024) · cites this paper as [31]
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References 31 · Cited by 484
- Authors
- Brown, B. D., Venneri, M. A., Zingale, A., Sergi, L. S., & Naldini, L.
- Affiliations
- The San Raffaele Telethon Institute for Gene Therapy (IT)
- Vita-Salute San Raffaele University (IT)
- Corresponding author
- Naldini, Luigi
- Venue
- Nature Medicine
- Published
- 2006-04-23
- Volume
- 12
- Issue
- 5
- Pages
- 585-591
- ISSN
- 1078-8956 (ISSN-L)
- 1546-170X
- OpenAlex
- W2171985637
- Cited by
- 484
- References
- 31
- Citations by year
- 2026: 15 · 2025: 9 · 2024: 7 · 2023: 12 · 2022: 17 · 2021: 17 · 2020: 15 · 2019: 15 · 2018: 22 · 2017: 22 · 2016: 18 · 2015: 34 · 2014: 32 · 2013: 46 · 2012: 33
- FWCI
- 17.27
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Medicine (publishedVersion)
- PubMed (publishedVersion)
- IRIS Research product catalog (Sapienza University of Rome) (submittedVersion)
- Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Keywords
- microRNA regulation, miR-142-3p, lentiviral vectors, hematopoietic lineage, stable gene transfer, gene therapy, vector design, tissue-specific gene expression, immunocompetent mice
- MeSH terms
- Animals, Gene Expression Regulation, Genetic Vectors, Hematopoietic Stem Cells, Liver, Mice, Inbred BALB C, Mice, Nude, Mice, Transgenic, Spleen, Lentivirus, Gene Transfer Techniques, Cell Lineage, Transgenes, MicroRNAs, Mice
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