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Genetic Engineering of Primary Mouse Intestinal Organoids Using Magnetic Nanoparticle Transduction Viral Vectors for Frozen Sectioning
Published on: May 10, 2019
Intracellular Delivery of Micron-Sized Magnetic Particles through a Virus Infection Pathway
Xiayi Feng1,2, Ding Gao1, Yipeng Jing3,4
1State Key Laboratory of Virology, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan 430071, PR China.
Abstract:
Micron-sized magnetic particles (M-MPs) have low toxicity, strong magnetic signals, and long-term retention capability, which are significant advantages for their application in biomedical imaging. Unfortunately, M-MPs are only internalized by few cell types, such as macrophages and phagocytes, and because of this lack of active intracellular delivery, their applications are restricted. The emergence of self-assembled virus-like particles (VLPs) offers a viable approach to drive M-MPs into cells, although the specific mechanism has not been revealed. In this study, we investigated in detail the intracellular pathway of M-MPs mediated by VLPs using a fluorescence co-localization method. The results indicated that the intracellular movement of M-MPs was consistent with the virus infection pathway, specifically caveolae-dependent endocytosis, transportation through microtubules, and accumulation in the endoplasmic reticulum. This study provides experimental support for the active transport of M-MPs into other cell types, thereby further extending their applications.
Insights
Virus-like particles (VLPs) enable micron-sized magnetic particles (M-MPs) to enter cells via a pathway mimicking viral infection. This breakthrough expands M-MP applications in biomedical imaging beyond traditional uptake cells.
Area of Science:
- Biomedical Imaging
- Nanotechnology
- Cell Biology
Background:
- Micron-sized magnetic particles (M-MPs) offer advantages like low toxicity and strong signals for biomedical imaging.
- Current limitations include restricted cellular uptake, primarily by macrophages and phagocytes, hindering broader applications.
- Virus-like particles (VLPs) present a potential solution for active intracellular delivery of M-MPs.
Purpose of the Study:
- To elucidate the intracellular pathway of M-MPs when delivered by VLPs.
- To investigate the mechanism of VLP-mediated M-MP internalization and transport.
- To provide evidence for active M-MP transport into non-phagocytic cells.
Main Methods:
- Utilized fluorescence co-localization techniques to track M-MP movement within cells.
- Analyzed the intracellular trafficking pathway of M-MPs mediated by VLPs.
- Compared M-MP pathway with known viral infection routes.
Main Results:
- VLP-mediated M-MP internalization followed a pathway characteristic of viral infection.
- The pathway involved caveolae-dependent endocytosis.
- Observed microtubule-dependent transport and accumulation in the endoplasmic reticulum.
Conclusions:
- VLPs facilitate active intracellular delivery of M-MPs into various cell types.
- The mechanism involves a virus-like endocytic pathway.
- This finding significantly broadens the potential applications of M-MPs in biomedical imaging and beyond.
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