Ischaemic heart disease evokes a complex immune response. However, tools to track the systemic behaviour and dynamics of leukocytes non-invasively in vivo are lacking. Here, we present a multimodal hot-spot imaging approach using an innovative high-density lipoprotein-derived nanotracer with a perfluoro-crown ether payload ((19)F-HDL) to allow myeloid cell tracking by (19)F magnetic resonance imaging. The (19)F-HDL nanotracer can additionally be labelled with zirconium-89 and fluorophores to detect myeloid cells by in vivo positron emission tomography imaging and optical modalities, respectively. Using our nanotracer in atherosclerotic mice with myocardial infarction, we observed rapid myeloid cell egress from the spleen and bone marrow by in vivo (19)F-HDL magnetic resonance imaging. Concurrently, using ex vivo techniques, we showed that circulating pro-inflammatory myeloid cells accumulated in atherosclerotic plaques and at the myocardial infarct site. Our multimodality imaging approach is a valuable addition to the immunology toolbox, enabling the study of complex myeloid cell behaviour dynamically.
Probing myeloid cell dynamics in ischaemic heart disease by nanotracer hot-spot imaging.
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作者:Senders Max L, Meerwaldt Anu E, van Leent Mandy M T, Sanchez-Gaytan Brenda L, van de Voort Jan C, Toner Yohana C, Maier Alexander, Klein Emma D, Sullivan Nathaniel A T, Sofias Alexandros Marios, Groenen Hannah, Faries Christopher, Oosterwijk Roderick S, van Leeuwen Esther M, Fay Francois, Chepurko Elena, Reiner Thomas, Duivenvoorden Raphael, Zangi Lior, Dijkhuizen Rick M, Hak Sjoerd, Swirski Filip K, Nahrendorf Matthias, Pérez-Medina Carlos, Teunissen Abraham J P, Fayad Zahi A, Calcagno Claudia, Strijkers Gustav J, Mulder Willem J M
| 期刊: | Nature Nanotechnology | 影响因子: | 34.900 |
| 时间: | 2020 | 起止号: | 2020 May;15(5):398-405 |
| doi: | 10.1038/s41565-020-0642-4 | ||
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