Estimating microtubule distributions from 2D immunofluorescence microscopy images reveals differences among human cultured cell lines.

Microtubules are filamentous structures that are involved in several important cellular processes, including cell division, cellular structure and mechanics, and intracellular transportation. Little is known about potential differences in microtubule distributions within and across cell lines. Here...

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Main Authors: Jieyue Li, Aabid Shariff, Mikaela Wiking, Emma Lundberg, Gustavo K Rohde, Robert F Murphy
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3508979?pdf=render
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spelling doaj-6789740c07f041599096f0cf1f8edbbf2020-11-25T01:53:29ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01711e5029210.1371/journal.pone.0050292Estimating microtubule distributions from 2D immunofluorescence microscopy images reveals differences among human cultured cell lines.Jieyue LiAabid ShariffMikaela WikingEmma LundbergGustavo K RohdeRobert F MurphyMicrotubules are filamentous structures that are involved in several important cellular processes, including cell division, cellular structure and mechanics, and intracellular transportation. Little is known about potential differences in microtubule distributions within and across cell lines. Here we describe a method to estimate information pertaining to 3D microtubule distributions from 2D fluorescence images. Our method allows for quantitative comparisons of microtubule distribution parameters (number of microtubules, mean length) between different cell lines. Among eleven cell lines compared, some showed differences that could be accounted for by differences in the total amount of tubulin per cell while others showed statistically significant differences in the balance between number and length of microtubules. We also observed that some cell lines that visually appear different in their microtubule distributions are quite similar when the model parameters are considered. The method is expected to be generally useful for comparing microtubule distributions between cell lines and for a given cell line after various perturbations. The results are also expected to enable analysis of the differences in gene expression underlying the observed differences in microtubule distributions among cell types.http://europepmc.org/articles/PMC3508979?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jieyue Li
Aabid Shariff
Mikaela Wiking
Emma Lundberg
Gustavo K Rohde
Robert F Murphy
spellingShingle Jieyue Li
Aabid Shariff
Mikaela Wiking
Emma Lundberg
Gustavo K Rohde
Robert F Murphy
Estimating microtubule distributions from 2D immunofluorescence microscopy images reveals differences among human cultured cell lines.
PLoS ONE
author_facet Jieyue Li
Aabid Shariff
Mikaela Wiking
Emma Lundberg
Gustavo K Rohde
Robert F Murphy
author_sort Jieyue Li
title Estimating microtubule distributions from 2D immunofluorescence microscopy images reveals differences among human cultured cell lines.
title_short Estimating microtubule distributions from 2D immunofluorescence microscopy images reveals differences among human cultured cell lines.
title_full Estimating microtubule distributions from 2D immunofluorescence microscopy images reveals differences among human cultured cell lines.
title_fullStr Estimating microtubule distributions from 2D immunofluorescence microscopy images reveals differences among human cultured cell lines.
title_full_unstemmed Estimating microtubule distributions from 2D immunofluorescence microscopy images reveals differences among human cultured cell lines.
title_sort estimating microtubule distributions from 2d immunofluorescence microscopy images reveals differences among human cultured cell lines.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Microtubules are filamentous structures that are involved in several important cellular processes, including cell division, cellular structure and mechanics, and intracellular transportation. Little is known about potential differences in microtubule distributions within and across cell lines. Here we describe a method to estimate information pertaining to 3D microtubule distributions from 2D fluorescence images. Our method allows for quantitative comparisons of microtubule distribution parameters (number of microtubules, mean length) between different cell lines. Among eleven cell lines compared, some showed differences that could be accounted for by differences in the total amount of tubulin per cell while others showed statistically significant differences in the balance between number and length of microtubules. We also observed that some cell lines that visually appear different in their microtubule distributions are quite similar when the model parameters are considered. The method is expected to be generally useful for comparing microtubule distributions between cell lines and for a given cell line after various perturbations. The results are also expected to enable analysis of the differences in gene expression underlying the observed differences in microtubule distributions among cell types.
url http://europepmc.org/articles/PMC3508979?pdf=render
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