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DOI 10.1021/acsnano.5c21042

Медицинская библиотека · ACS nano · 2026

Trans-Endothelial Trafficking in Zebrafish: Nanobio Interactions of Polyethylene Glycol-Based Nanoparticles in Live Vasculature.

Lim Ye-Wheen, Bell Craig A, Fletcher Nicholas L, Condon Nicholas D, Akhter Dewan T, Rae James, Ferguson Charles, Martel Nick, Humphries James, Lo Harriet P, Wu Yeping, Houston Zachary H, Lagendijk Anne K, Hall Thomas E, Thurecht Kristofer J, Parton Robert G

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Аннотация

Trans-endothelial transport of nanoparticles remains poorly characterized in live organisms. The zebrafish is a well-established model for direct in vivo imaging; however, standardized controls have not been consistently applied across studies. Here, we developed a standardized protocol to assess nanoparticle trans-endothelial trafficking in live zebrafish. We identified 2000 kDa dextran as an optimal coinjection control for standardizing microinjections and quantifying nanoparticle transport in a systematic, unbiased manner. Using the standardized protocol, we profiled early physiological trans-endothelial transport pathways in zebrafish embryos using dextran solutes as extravasation markers, showing that steady-state solute extravasation is characterized by paracellular routes selective for solutes <15 nm in diameter, dynamin-mediated endocytosis, and low basal macropinocytosis. We assessed the extravasation of 3, 7, 32, 47, 81, and 109 nm polyethylene glycol (PEG)-based nanoparticles using this protocol. Using a pretreatment protocol with chemical inhibitors, we demonstrate that <7 nm PEG-based hyperbranched polymer (HBP) nanoparticles undergo rapid paracellular extravasation, 32 to 81 nm PEG-based micelles adopt dynamin-dependent and macropinocytic trafficking over paracellular transport, and 109 nm PEG-based micelles extravasate primarily via macropinocytic trafficking. We characterized the emergence of vascular caveolae up to 17 days postfertilization with a cavin1b knock-in zebrafish line. Using cavin1a/cavin1b double knockout zebrafish and tumor-bearing Cavin1 null mice, we showed that caveolae do not contribute to the transvascular transport of these PEG-based nanoparticles. This work demonstrates the rigor of the standardized protocol for assessing trans-endothelial transport in the live zebrafish and provides fundamental cell biology insight into the in vivo behavior of PEG-based nanoparticles.

Для цитирования: Lim Ye-Wheen, Bell Craig A, Fletcher Nicholas L, Condon Nicholas D, Akhter Dewan T, Rae James, Ferguson Charles, Martel Nick, Humphries James, Lo Harriet P, Wu Yeping, Houston Zachary H, Lagendijk Anne K, Hall Thomas E, Thurecht Kristofer J, Parton Robert G. Trans-Endothelial Trafficking in Zebrafish: Nanobio Interactions of Polyethylene Glycol-Based Nanoparticles in Live Vasculature.. ACS nano. 2026. DOI: 10.1021/acsnano.5c21042.

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