Journal of Innovative Optical Health Sciences, Volume. 14, Issue 6, 2150017(2021)
Fusion of clathrin and caveolae endocytic vesicles revealed by line-switching dual-color STED microscopy
[1] [1] G. J. Doherty, H. T. McMahon, "Mechanisms of Endocytosis," Annu. Rev. Biochem. 78, 857–902 (2009).
[2] [2] J. L. Goldstein, R. G. W. Anderson, M. S. Brown, "Coated pits, coated vesicles, and receptor-mediated endocytosis," Nature 279, 679–685 (1979).
[3] [3] R. C. Aguilar, B. Wendland, "Endocytosis of membrane receptors: Two pathways are better than one," Proc. Natl. Acad. Sci. USA 102, 2679–2680 (2005).
[4] [4] K. Sandvig, M. L. Torgersen, H. A. Raa, B. Van Deurs, "Clathrin-independent endocytosis: From nonexisting to an extreme degree of complexity," Histochem. Cell Biol. 129, 267–276 (2008).
[5] [5] T. A. Klar, S. Jakobs, M. Dyba, A. Egner, S. W. Hell, "Fluorescence microscopy with diffraction resolution barrier broken by stimulated emission," Proc. Natl. Acad. Sci. USA 97, 8206–8210 (2000).
[6] [6] S. W. Hell, "Far-field optical nanoscopy," Science 316, 1153–1158 (2007).
[7] [7] S. W. Hell, S. J. Sahl, M. Bates, X. Zhuang, R. Heintzmann, M. J. Booth, J. Bewersdorf, G. Shtengel, H. Hess, P. Tinnefeld, A. Honigmann, S. Jakobs, I. Testa, L. Cognet, B. Lounis, H. Ewers, S. J. Davis, C. Eggeling, D. Klenerman, K. I. Willig, G. Vicidomini, M. Castello, A. Diaspro, T. Cordes, "The 2015 super-resolution microscopy roadmap," J. Phys. D, Appl. Phys. 48, 443001 (2015).
[8] [8] B. Hein, K. I. Willig, S. W. Hell, "Stimulated emission depletion (STED) nanoscopy of a fluorescent protein-labeled organelle inside a living cell," Proc. Natl. Acad. Sci. USA 105, 14271–14276 (2008).
[9] [9] V. Westphal, S. O. Rizzoli, M. A. Lauterbach, D. Kamin, R. Jahn, S. W. Hell, "Video-rate far-field optical nanoscopy dissects synaptic vesicle movement," Science 320, 246–249 (2008).
[10] [10] G. Donnert, J. Keller, C. A. Wurm, S. O. Rizzoli, V. Westphal, A. Schoenle, R. Jahn, S. Jakobs, C. Eggeling, S. W. Hell, "Two-color far-field fluorescence nanoscopy," Biophys. J. 92, L67–L69 (2007).
[11] [11] R. Schmidt, C. A. Wurm, S. Jakobs, J. Engelhardt, A. Egner, S. W. Hell, "Spherical nanosized focal spot unravels the interior of cells," Nat. Methods 5, 539– 544 (2008).
[12] [12] D. Neumann, J. Buckers, L. Kastrup, S. W. Hell, S. Jakobs, "Two-color STED microscopy reveals different degrees of colocalization between hexokinase-I and the three human VDAC isoforms," PMC Biophys. 3, 4–4 (2010).
[13] [13] D. C. Jans, C. A. Wurm, D. Riedel, D. Wenzel, F. Stagge, M. Deckers, P. Rehling, S. Jakobs, "STED super-resolution microscopy reveals an array of MINOS clusters along human mitochondria," Proc. Natl. Acad. Sci. USA 110, 8936–8941 (2013).
[14] [14] F. Goettfert, C. A. Wurm, V. Mueller, S. Berning, V. C. Cordes, A. Honigmann, S. W. Hell, "Coaligned dual-channel STED nanoscopy and molecular diffusion analysis at 20 nm resolution," Biophys. J. 105, L1–L3 (2013).
[15] [15] G. Donnert, J. Keller, R. Medda, M. A. Andrei, S. O. Rizzoli, R. Luehrmann, R. Jahn, C. Eggeling, S. W. Hell, "Macromolecular-scale resolution in biological fluorescence microscopy," Proc. Natl. Acad. Sci. USA 103, 11440–11445 (2006).
[16] [16] G. Donnert, C. Eggeling, S. W. Hell, "Major signal increase in fluorescence microscopy through darkstate relaxation," Nat. Methods 4, 81–86 (2007).
[17] [17] P. A. Pellett, X. Sun, T. J. Gould, J. E. Rothman, M.-Q. Xu, I. R. Correa, Jr., J. Bewersdorf, "Twocolor STED microscopy in living cells," Biomed. Opt. Express 2, 2364–2371 (2011).
[18] [18] J. Bueckers, D. Wildanger, G. Vicidomini, L. Kastrup, S. W. Hell, "Simultaneous multi-lifetime multi-color STED imaging for colocalization analyses," Opt. Express 19, 3130–3143 (2011).
[19] [19] K. S. Y. Liu, M. Siebert, S. Mertel, E. Knoche, S. Wegener, C. Wichmann, T. Matkovic, K. Muhammad, H. Depner, C. Mettke, J. Bueckers, S. W. Hell, M. Mueller, G. W. Davis, D. Schmitz, S. J. Sigrist, "RIM-binding protein, a central part of the active zone, is essential for neurotransmitter release," Science 334, 1565–1569 (2011).
[20] [20] J. Tonnesen, F. Nadrigny, K. I. Willig, R. Wedlich- Soeldner, U. V. Naegerl, "Two-color STED microscopy of living synapses using a single laser-beam pair," Biophys. J. 101, 2545–2552 (2011).
[21] [21] A. N. Butkevich, G. Y. Mitronova, S. C. Sidenstein, J. L. Klocke, D. Kamin, D. N. H. Meineke, E. D'Este, P.-T. Kraemer, J. G. Danzl, V. N. Belov, S. W. Hell, "Fluorescent rhodamines and fluorogenic carbopyronines for super-resolution STED microscopy in living cells," Angew. Chem. Int. Edit. 55, 3290–3294 (2016).
[22] [22] J. A. Torreno-Pina, C. Manzo, M. Salio, M. C. Aichinger, A. Oddone, M. Lakadamyali, D. Shepherd, G. S. Besra, V. Cerundolo, M. F. Garcia-Parajo, "The actin cytoskeleton modulates the activation of iNKT cells by segregating CD1d nanoclusters on antigenpresenting cells," Proc. Natl. Acad. Sci. USA 113, E772–E781 (2016).
[23] [23] J. Fischer, J. B. Mueller, A. S. Quick, J. Kaschke, C. Barner-Kowollik, M. Wegener, "Exploring the mechanisms in STED-enhanced direct laser writing," Adv. Opt. Mater. 3, 221–232 (2015).
[24] [24] D. Wildanger, E. Rittweger, L. Kastrup, S. W. Hell, "STED microscopy with a supercontinuum laser source," Opt. Express 16, 9614–9621 (2008).
[25] [25] D. Wildanger, R. Medda, L. Kastrup, S. W. Hell, "A compact STED microscope providing 3D nanoscale resolution," J. Microsc. (Oxford) 236, 35–43 (2009).
[26] [26] J. Yu, J. Yuan, X. Zhang, J. Liu, X. Fang, "Nanoscale imaging with an integrated system combining stimulated emission depletion microscope and atomic force microscope," Chin. Sci. Bull. 58, 4045–4050 (2013).
[27] [27] H. Ruan, J. Yu, J. Yuan, N. Li, X. Fang, "Nanoscale distribution of transforming growth factor receptor on post-Golgi vesicle revealed by super-resolution microscopy," Chem.-Asian J. 11, 3359–3364 (2016).
[28] [28] Y. Wu, H. Ruan, R. Zhao, Z. Dong, W. Li, X. Tang, J. Yuan, X. Fang, "Ultrastable fluorescent polymer dots for stimulated emission depletion bioimaging," Adv. Opt. Mater. 6, 1800333 (2018).
[29] [29] Y. Wu, H. Ruan, Z. Dong, R. Zhao, J. Yu, X. Tang, X. Kou, X. Zhang, M. Wu, F. Luo, J. Yuan, X. Fang, "Fluorescent polymer dot-based multicolor stimulated emission depletion nanoscopy with a single laser beam pair for cellular tracking," Anal. Chem. 92, 12088–12096 (2020).
[30] [30] C. Chen, "Clathrin meets caveolae: Fuse or not?," Sci. Bull. 60, 1787–1788 (2015).
[31] [31] K. He, X. Yan, N. Li, S. Dang, L. Xu, B. Zhao, Z. Li, Z. Lv, X. Fang, Y. Zhang, Y.-G. Chen, "Internalization of the TGF-beta type I receptor into caveolin-1 and EEA1 double-positive early endosomes," Cell Res. 25, 738–752 (2015).
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Hefei Ruan, Jianqiang Yu, Yayun Wu, Xiaojun Tang, Jinghe Yuan, Xiaohong Fang. Fusion of clathrin and caveolae endocytic vesicles revealed by line-switching dual-color STED microscopy[J]. Journal of Innovative Optical Health Sciences, 2021, 14(6): 2150017
Received: Apr. 26, 2021
Accepted: May. 28, 2021
Published Online: Dec. 6, 2021
The Author Email: Yuan Jinghe (jhyuan@iccas.ac.cn)