Optical micromanipulation of nanoparticles and cells inside living zebrafish

Nature Communications

Volumn 7, Issue , 2016, Pages

  Johansen, Patrick Lie ^a   Fenaroli, Federico ^a   Evensen, Lasse ^a   Griffiths, Gareth ^a   Koster, Gerbrand ^a,b  

^a UNIVERSITY OF OSLO   (Norway)

^b Inven2 AS   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

NANOPARTICLE; NANOTUBE;

ADHESION; BIOACCUMULATION; BIOTECHNOLOGY; CANCER; CELLS AND CELL COMPONENTS; CYPRINID; EMBRYO; MEMBRANE; NANOPARTICLE; OPTICAL PROPERTY;

ANIMAL CELL; ARTICLE; CELL ADHESION; CELL INTERACTION; CELL MEMBRANE; CONTROLLED STUDY; EMBRYO; ENDOTHELIUM; MACROPHAGE; MICROMANIPULATION; NEOPLASM; NONHUMAN; OPTICAL TWEEZERS; ZEBRA FISH; ANIMAL; CHEMISTRY; ERYTHROCYTE; METABOLISM; MICROINJECTION; PROCEDURES; TRANSGENIC ANIMAL;

DANIO RERIO;

ANIMALS; ANIMALS, GENETICALLY MODIFIED; ERYTHROCYTES; MACROPHAGES; MICROINJECTIONS; MICROMANIPULATION; NANOPARTICLES; NANOTUBES; OPTICAL TWEEZERS; ZEBRAFISH;

EID: 84961743064     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms10974     Document Type: Article

References (34)

1. Pober, J. S., Sessa, W. C. Evolving functions of endothelial cells in inflammation. Nat. Rev. Immunol. 7, 803-815 (2007).
2. Ashkin, A., Dziedzic, J. M. Optical trapping and manipulation of viruses and bacteria. Science 235, 1517-1520 (1987).
3. Bendix, P. M., Jauffred, L., Norregaard, K., Oddershede, L. B. Optical trapping of nanoparticles and quantum dots. IEEE J. Sel. Top. Quantum Electron. 20, 15-26 (2014).
4. Blehm, B. H., Schroer, T. A., Trybus, K. M., Chemla, Y. R., Selvin, P. R. In vivo optical trapping indicates kinesin's stall force is reduced by dynein during intracellular transport. Proc. Natl Acad. Sci. USA 110, 3381-3386 (2013).
5. Hendricks, A. G., Holzbaur, E. L., Goldman, Y. E. Force measurements on cargoes in living cells reveal collective dynamics of microtubule motors. Proc. Natl Acad. Sci. USA 109, 18447-18452 (2012).
6. Oddershede, L. B. Force probing of individual molecules inside the living cell is now a reality. Nat. Chem. Biol. 8, 879-886 (2012).
7. Hansen, P. M., Oddershede, L. B. Optical trapping inside living organisms. Proc. SPIE 5930, 1-9 (2005).
8. Zhong, M. C., Wei, X. B., Zhou, J. H., Wang, Z. Q., Li, Y. M. Trapping red blood cells in living animals using optical tweezers. Nat. Commun. 4, 1768 (2013).
9. Liu, S., Leach, S. D. Zebrafish models for cancer. Annu. Rev. Pathol. Mech. Dis. 6, 71-93 (2011).
10. Lieschke, G. J., Currie, P. D. Animal models of human disease: zebrafish swim into view. Nat. Rev. Genet. 8, 353-367 (2007).
11. Evensen, L. et al. Zebrafish as a model system for characterization of nanoparticles against cancer. Nanoscale 8, 862-877 (2015).
12. Fenaroli, F. et al. Nanoparticles as drug delivery system against tuberculosis in zebrafish embryos: direct visualization and treatment. ACS Nano 8, 7014-7026 (2014).
13. Kamaly, N., Xiao, Z., Valencia, P. M., Radovic-Moreno, A. F., Farokhzad, O. C. Targeted polymeric therapeutic nanoparticles: design, development and clinical translation. Chem. Soc. Rev. 41, 2971-3010 (2012).
14. Fieramonti, L. et al. Quantitative measurement of blood velocity in zebrafish with optical vector field tomography. J Biophoton. 8, 52-59 (2015).
15. Koster, G., Cacciuto, A., Derenyi, I., Frenkel, D., Dogterom, M. Force barriers for membrane tube formation. Phys. Rev. Lett. 94, 068101 (2005).
16. Visscher, K., Gross, S. P., Block, S. M. Construction of multiple-beam optical traps with nanometer-resolution position sensing. IEEE J. Sel. Top. Quantum Electron. 2, 1066-1076 (1996).
17. Rohrbach, A. Stiffness of optical traps: quantitative agreement between experiment and electromagnetic theory. Phys. Rev. Lett. 95, 168102 (2005).
18. Cosma, C. L., Swaim, L. E., Volkman, H., Ramakrishnan, L., Davis, J. M. Zebrafish and frog models of Mycobacterium marinum infection. Curr. Protoc. Microbiol. Chapter 10, Unit 10B.2 (2006).
19. Zon, L. I. Developmental biology of hematopoiesis. Blood 86, 2876-2891 (1995).
20. Oyama, K. et al. Directional bleb formation in spherical cells under temperature gradient. Biophys. J. 109, 355-364 (2015).
21. Sorre, B. et al. Curvature-driven lipid sorting needs proximity to a demixing point and is aided by proteins. Proc. Natl Acad. Sci. USA 106, 5622-5626 (2009).
22. Ellett, F., Pase, L., Hayman, J. W., Andrianopoulos, A., Lieschke, G. J. mpeg1 promoter transgenes direct macrophage-lineage expression in zebrafish. Blood 117, e49-e56 (2011).
23. Lawson, N. D., Weinstein, B. M. In vivo imaging of embryonic vascular development using transgenic zebrafish. Dev. Biol. 248, 307-318 (2002).
24. Desjardins, M., Griffiths, G. Phagocytosis: latex leads the way. Curr. Opin. Cell Biol. 15, 498-503 (2003).
25. Chaudhuri, O., Parekh, S. H., Lam, W. A., Fletcher, D. A. Combined atomic force microscopy and side-view optical imaging for mechanical studies of cells. Nat. Methods 6, 383-387 (2009).
26. Davis, D. M., Sowinski, S. Membrane nanotubes: dynamic long-distance connections between animal cells. Nat. Rev. Mol. Cell Biol. 9, 431-436 (2008).
27. Derényi, I. et al. in Controlled nanoscale motion Vol. 711 Lecture Notes in Physics. (eds Linke, H., Månsson, A.) Ch. 7 141-159 (Springer Berlin Heidelberg, 2007).
28. Pontes, B. et al. Membrane elastic properties and cell function. PLoS ONE 8, e67708 (2013).
29. Xu, D., Esko, J. D. Demystifying heparan sulfate-protein interactions. Annu. Rev. Biochem. 83, 129-157 (2014).
30. Ramakrishnan, L. Looking within the zebrafish to understand the tuberculous granuloma. Adv. Exp. Med. Biol. 783, 251-266 (2013).
31. Herbomel, P., Thisse, B., Thisse, C. Ontogeny and behaviour of early macrophages in the zebrafish embryo. Development 126, 3735-3745 (1999).
32. Cordero-Maldonado, M. L. et al. Optimization and pharmacological validation of a leukocyte migration assay in zebrafish larvae for the rapid in vivo bioactivity analysis of anti-inflammatory secondary metabolites. PLoS ONE 8, e75404 (2013).
33. Kress, H. et al. Cell stimulation with optically manipulated microsources. Nat. Methods 6, 905-909 (2009).
34. Karlsson, J., von Hofsten, J., Olsson, P.-E. Generating transparent zebrafish: a refined method to improve detection of gene expression during embryonic development. Mar. Biotechnol. 3, 522-527 (2001).