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Quantitative Analysis of Nuclear Lamins Imaged by Super-Resolution Light Microscopy

The nuclear lamina consists of a dense fibrous meshwork of nuclear lamins, Type V intermediate filaments, and is ~14 nm thick according to recent cryo-electron tomography studies. Recent advances in light microscopy have extended the resolution to a scale allowing for the fine structure of the lamin...

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Detalles Bibliográficos
Autores principales: Kittisopikul, Mark, Virtanen, Laura, Taimen, Pekka, Goldman, Robert D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524165/
https://www.ncbi.nlm.nih.gov/pubmed/31003483
http://dx.doi.org/10.3390/cells8040361
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author Kittisopikul, Mark
Virtanen, Laura
Taimen, Pekka
Goldman, Robert D.
author_facet Kittisopikul, Mark
Virtanen, Laura
Taimen, Pekka
Goldman, Robert D.
author_sort Kittisopikul, Mark
collection PubMed
description The nuclear lamina consists of a dense fibrous meshwork of nuclear lamins, Type V intermediate filaments, and is ~14 nm thick according to recent cryo-electron tomography studies. Recent advances in light microscopy have extended the resolution to a scale allowing for the fine structure of the lamina to be imaged in the context of the whole nucleus. We review quantitative approaches to analyze the imaging data of the nuclear lamina as acquired by structured illumination microscopy (SIM) and single molecule localization microscopy (SMLM), as well as the requisite cell preparation techniques. In particular, we discuss the application of steerable filters and graph-based methods to segment the structure of the four mammalian lamin isoforms (A, C, B1, and B2) and extract quantitative information.
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spelling pubmed-65241652019-06-03 Quantitative Analysis of Nuclear Lamins Imaged by Super-Resolution Light Microscopy Kittisopikul, Mark Virtanen, Laura Taimen, Pekka Goldman, Robert D. Cells Review The nuclear lamina consists of a dense fibrous meshwork of nuclear lamins, Type V intermediate filaments, and is ~14 nm thick according to recent cryo-electron tomography studies. Recent advances in light microscopy have extended the resolution to a scale allowing for the fine structure of the lamina to be imaged in the context of the whole nucleus. We review quantitative approaches to analyze the imaging data of the nuclear lamina as acquired by structured illumination microscopy (SIM) and single molecule localization microscopy (SMLM), as well as the requisite cell preparation techniques. In particular, we discuss the application of steerable filters and graph-based methods to segment the structure of the four mammalian lamin isoforms (A, C, B1, and B2) and extract quantitative information. MDPI 2019-04-18 /pmc/articles/PMC6524165/ /pubmed/31003483 http://dx.doi.org/10.3390/cells8040361 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Kittisopikul, Mark
Virtanen, Laura
Taimen, Pekka
Goldman, Robert D.
Quantitative Analysis of Nuclear Lamins Imaged by Super-Resolution Light Microscopy
title Quantitative Analysis of Nuclear Lamins Imaged by Super-Resolution Light Microscopy
title_full Quantitative Analysis of Nuclear Lamins Imaged by Super-Resolution Light Microscopy
title_fullStr Quantitative Analysis of Nuclear Lamins Imaged by Super-Resolution Light Microscopy
title_full_unstemmed Quantitative Analysis of Nuclear Lamins Imaged by Super-Resolution Light Microscopy
title_short Quantitative Analysis of Nuclear Lamins Imaged by Super-Resolution Light Microscopy
title_sort quantitative analysis of nuclear lamins imaged by super-resolution light microscopy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524165/
https://www.ncbi.nlm.nih.gov/pubmed/31003483
http://dx.doi.org/10.3390/cells8040361
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