| Literature DB >> 30735894 |
Hyeon Jin Jeong1, Ran Ji Yoo2, Jin Kwan Kim1, Min Hwan Kim2, Su Hong Park1, Haebin Kim1, Jae Wook Lim1, Sun Hee Do3, Kyo Chul Lee2, Yong Jin Lee4, Dong Wook Kim5.
Abstract
We introduce an efficient cell tracking imaging protocol using positron emission tomography (PET). Since macrophages are known to home and accumulate in tumor tissues and atherosclerotic plaque, we design a PET imaging protocol for macrophage cell tracking using aza-dibenzocyclooctyne-tethered PEGylated mesoporous silica nanoparticles (DBCO-MSNs) with the short half-life F-18-labeled azide-radiotracer via an in vivo strain-promoted alkyne azide cycloaddition (SPAAC) covalent labeling reaction inside macrophage cells in vivo. This PET imaging protocol for in vivo cell tracking successfully visualizes the migration of macrophage cells into the tumor site by the bioorthogonal SPAAC reaction of DBCO-MSNs with [18F]fluoropentaethylene glycolic azide ([18F]2) to form 18F-labeled aza-dibenzocycloocta-triazolic MSNs (18F-DBCOT-MSNs) inside RAW 264.7 cells. The tissue radioactivity distribution results were consistent with PET imaging findings. In addition, PET images of atherosclerosis in ApoE-/- mice fed a western diet for 30 weeks were obtained using the devised macrophage cell-tracking protocol.Entities:
Keywords: Bioothogonal labeling; Cell tracking; Fluorine-18; Macrophage cells; Mesoporous silica nanoparticles; PET molecular imaging
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Year: 2019 PMID: 30735894 DOI: 10.1016/j.biomaterials.2019.01.043
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479