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Revealing Nanoscale Morphology of the Primary Cilium Using Super-Resolution Fluorescence Microscopy

Super-resolution (SR) microscopy has been used to observe structural details beyond the diffraction limit of ∼250 nm in a variety of biological and materials systems. By combining this imaging technique with both computer-vision algorithms and topological methods, we reveal and quantify the nanoscal...

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Autores principales: Yoon, Joshua, Comerci, Colin J., Weiss, Lucien E., Milenkovic, Ljiljana, Stearns, Tim, Moerner, W.E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Biophysical Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349968/
https://www.ncbi.nlm.nih.gov/pubmed/30598282
http://dx.doi.org/10.1016/j.bpj.2018.11.3136
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author Yoon, Joshua
Comerci, Colin J.
Weiss, Lucien E.
Milenkovic, Ljiljana
Stearns, Tim
Moerner, W.E.
author_facet Yoon, Joshua
Comerci, Colin J.
Weiss, Lucien E.
Milenkovic, Ljiljana
Stearns, Tim
Moerner, W.E.
author_sort Yoon, Joshua
collection PubMed
description Super-resolution (SR) microscopy has been used to observe structural details beyond the diffraction limit of ∼250 nm in a variety of biological and materials systems. By combining this imaging technique with both computer-vision algorithms and topological methods, we reveal and quantify the nanoscale morphology of the primary cilium, a tiny tubular cellular structure (∼2–6 μm long and 200–300 nm in diameter). The cilium in mammalian cells protrudes out of the plasma membrane and is important in many signaling processes related to cellular differentiation and disease. After tagging individual ciliary transmembrane proteins, specifically Smoothened, with single fluorescent labels in fixed cells, we use three-dimensional (3D) single-molecule SR microscopy to determine their positions with a precision of 10–25 nm. We gain a dense, pointillistic reconstruction of the surfaces of many cilia, revealing large heterogeneity in membrane shape. A Poisson surface reconstruction algorithm generates a fine surface mesh, allowing us to characterize the presence of deformations by quantifying the surface curvature. Upon impairment of intracellular cargo transport machinery by genetic knockout or small-molecule treatment of cells, our quantitative curvature analysis shows significant morphological differences not visible by conventional fluorescence microscopy techniques. Furthermore, using a complementary SR technique, two-color, two-dimensional stimulated emission depletion microscopy, we find that the cytoskeleton in the cilium, the axoneme, also exhibits abnormal morphology in the mutant cells, similar to our 3D results on the Smoothened-measured ciliary surface. Our work combines 3D SR microscopy and computational tools to quantitatively characterize morphological changes of the primary cilium under different treatments and uses stimulated emission depletion to discover correlated changes in the underlying structure. This approach can be useful for studying other biological or nanoscale structures of interest.
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spelling pubmed-63499682020-01-22 Revealing Nanoscale Morphology of the Primary Cilium Using Super-Resolution Fluorescence Microscopy Yoon, Joshua Comerci, Colin J. Weiss, Lucien E. Milenkovic, Ljiljana Stearns, Tim Moerner, W.E. Biophys J Articles Super-resolution (SR) microscopy has been used to observe structural details beyond the diffraction limit of ∼250 nm in a variety of biological and materials systems. By combining this imaging technique with both computer-vision algorithms and topological methods, we reveal and quantify the nanoscale morphology of the primary cilium, a tiny tubular cellular structure (∼2–6 μm long and 200–300 nm in diameter). The cilium in mammalian cells protrudes out of the plasma membrane and is important in many signaling processes related to cellular differentiation and disease. After tagging individual ciliary transmembrane proteins, specifically Smoothened, with single fluorescent labels in fixed cells, we use three-dimensional (3D) single-molecule SR microscopy to determine their positions with a precision of 10–25 nm. We gain a dense, pointillistic reconstruction of the surfaces of many cilia, revealing large heterogeneity in membrane shape. A Poisson surface reconstruction algorithm generates a fine surface mesh, allowing us to characterize the presence of deformations by quantifying the surface curvature. Upon impairment of intracellular cargo transport machinery by genetic knockout or small-molecule treatment of cells, our quantitative curvature analysis shows significant morphological differences not visible by conventional fluorescence microscopy techniques. Furthermore, using a complementary SR technique, two-color, two-dimensional stimulated emission depletion microscopy, we find that the cytoskeleton in the cilium, the axoneme, also exhibits abnormal morphology in the mutant cells, similar to our 3D results on the Smoothened-measured ciliary surface. Our work combines 3D SR microscopy and computational tools to quantitatively characterize morphological changes of the primary cilium under different treatments and uses stimulated emission depletion to discover correlated changes in the underlying structure. This approach can be useful for studying other biological or nanoscale structures of interest. The Biophysical Society 2019-01-22 2018-12-07 /pmc/articles/PMC6349968/ /pubmed/30598282 http://dx.doi.org/10.1016/j.bpj.2018.11.3136 Text en © 2018 Biophysical Society. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles
Yoon, Joshua
Comerci, Colin J.
Weiss, Lucien E.
Milenkovic, Ljiljana
Stearns, Tim
Moerner, W.E.
Revealing Nanoscale Morphology of the Primary Cilium Using Super-Resolution Fluorescence Microscopy
title Revealing Nanoscale Morphology of the Primary Cilium Using Super-Resolution Fluorescence Microscopy
title_full Revealing Nanoscale Morphology of the Primary Cilium Using Super-Resolution Fluorescence Microscopy
title_fullStr Revealing Nanoscale Morphology of the Primary Cilium Using Super-Resolution Fluorescence Microscopy
title_full_unstemmed Revealing Nanoscale Morphology of the Primary Cilium Using Super-Resolution Fluorescence Microscopy
title_short Revealing Nanoscale Morphology of the Primary Cilium Using Super-Resolution Fluorescence Microscopy
title_sort revealing nanoscale morphology of the primary cilium using super-resolution fluorescence microscopy
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349968/
https://www.ncbi.nlm.nih.gov/pubmed/30598282
http://dx.doi.org/10.1016/j.bpj.2018.11.3136
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