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Automatic morphological subtyping reveals new roles of caspases in mitochondrial dynamics
Morphological dynamics of mitochondria is associated with key cellular processes related to aging and neuronal degenerative diseases, but the lack of standard quantification of mitochondrial morphology impedes systematic investigation. This paper presents an automated system for the quantification a...
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Published in: | PLoS computational biology 2011-10, Vol.7 (10), p.e1002212-e1002212 |
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creator | Peng, Jyh-Ying Lin, Chung-Chih Chen, Yen-Jen Kao, Lung-Sen Liu, Young-Chau Chou, Chung-Chien Huang, Yi-Hung Chang, Fang-Rong Wu, Yang-Chang Tsai, Yuh-Show Hsu, Chun-Nan |
description | Morphological dynamics of mitochondria is associated with key cellular processes related to aging and neuronal degenerative diseases, but the lack of standard quantification of mitochondrial morphology impedes systematic investigation. This paper presents an automated system for the quantification and classification of mitochondrial morphology. We discovered six morphological subtypes of mitochondria for objective quantification of mitochondrial morphology. These six subtypes are small globules, swollen globules, straight tubules, twisted tubules, branched tubules and loops. The subtyping was derived by applying consensus clustering to a huge collection of more than 200 thousand mitochondrial images extracted from 1422 micrographs of Chinese hamster ovary (CHO) cells treated with different drugs, and was validated by evidence of functional similarity reported in the literature. Quantitative statistics of subtype compositions in cells is useful for correlating drug response and mitochondrial dynamics. Combining the quantitative results with our biochemical studies about the effects of squamocin on CHO cells reveals new roles of Caspases in the regulatory mechanisms of mitochondrial dynamics. This system is not only of value to the mitochondrial field, but also applicable to the investigation of other subcellular organelle morphology. |
doi_str_mv | 10.1371/journal.pcbi.1002212 |
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This paper presents an automated system for the quantification and classification of mitochondrial morphology. We discovered six morphological subtypes of mitochondria for objective quantification of mitochondrial morphology. These six subtypes are small globules, swollen globules, straight tubules, twisted tubules, branched tubules and loops. The subtyping was derived by applying consensus clustering to a huge collection of more than 200 thousand mitochondrial images extracted from 1422 micrographs of Chinese hamster ovary (CHO) cells treated with different drugs, and was validated by evidence of functional similarity reported in the literature. Quantitative statistics of subtype compositions in cells is useful for correlating drug response and mitochondrial dynamics. Combining the quantitative results with our biochemical studies about the effects of squamocin on CHO cells reveals new roles of Caspases in the regulatory mechanisms of mitochondrial dynamics. This system is not only of value to the mitochondrial field, but also applicable to the investigation of other subcellular organelle morphology.</description><identifier>ISSN: 1553-7358</identifier><identifier>ISSN: 1553-734X</identifier><identifier>EISSN: 1553-7358</identifier><identifier>DOI: 10.1371/journal.pcbi.1002212</identifier><identifier>PMID: 21998575</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Aging ; Animals ; Apoptosis ; Automation ; Biology ; Caspase Inhibitors ; Caspases - metabolism ; Cellular biology ; Cellular signal transduction ; CHO Cells ; Classification ; Computational Biology ; Computer Science ; Cricetinae ; Cricetulus ; Cysteine Proteinase Inhibitors - pharmacology ; Degeneration ; Dimethyl Sulfoxide - pharmacology ; Experiments ; Furans - pharmacology ; Genetic aspects ; Lactones - pharmacology ; Mitochondria ; Mitochondria - classification ; Mitochondria - drug effects ; Mitochondria - enzymology ; Mitochondria - ultrastructure ; Mitochondrial DNA ; Models, Biological ; Nervous system ; Oligopeptides - pharmacology ; Pattern Recognition, Automated - statistics & numerical data ; Physiological aspects ; Proteins ; Studies</subject><ispartof>PLoS computational biology, 2011-10, Vol.7 (10), p.e1002212-e1002212</ispartof><rights>COPYRIGHT 2011 Public Library of Science</rights><rights>Peng et al. 2011</rights><rights>2011 Peng et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Peng J-Y, Lin C-C, Chen Y-J, Kao L-S, Liu Y-C, et al. (2011) Automatic Morphological Subtyping Reveals New Roles of Caspases in Mitochondrial Dynamics. PLoS Comput Biol 7(10): e1002212. doi:10.1371/journal.pcbi.1002212</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c698t-ff88bbd8911222da8159290032c17a063b0baa691a6a72b9591eb2cc5d470e8e3</citedby><cites>FETCH-LOGICAL-c698t-ff88bbd8911222da8159290032c17a063b0baa691a6a72b9591eb2cc5d470e8e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3188504/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3188504/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,37013,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21998575$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Covert, Markus W.</contributor><creatorcontrib>Peng, Jyh-Ying</creatorcontrib><creatorcontrib>Lin, Chung-Chih</creatorcontrib><creatorcontrib>Chen, Yen-Jen</creatorcontrib><creatorcontrib>Kao, Lung-Sen</creatorcontrib><creatorcontrib>Liu, Young-Chau</creatorcontrib><creatorcontrib>Chou, Chung-Chien</creatorcontrib><creatorcontrib>Huang, Yi-Hung</creatorcontrib><creatorcontrib>Chang, Fang-Rong</creatorcontrib><creatorcontrib>Wu, Yang-Chang</creatorcontrib><creatorcontrib>Tsai, Yuh-Show</creatorcontrib><creatorcontrib>Hsu, Chun-Nan</creatorcontrib><title>Automatic morphological subtyping reveals new roles of caspases in mitochondrial dynamics</title><title>PLoS computational biology</title><addtitle>PLoS Comput Biol</addtitle><description>Morphological dynamics of mitochondria is associated with key cellular processes related to aging and neuronal degenerative diseases, but the lack of standard quantification of mitochondrial morphology impedes systematic investigation. 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This system is not only of value to the mitochondrial field, but also applicable to the investigation of other subcellular organelle morphology.</description><subject>Aging</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Automation</subject><subject>Biology</subject><subject>Caspase Inhibitors</subject><subject>Caspases - metabolism</subject><subject>Cellular biology</subject><subject>Cellular signal transduction</subject><subject>CHO Cells</subject><subject>Classification</subject><subject>Computational Biology</subject><subject>Computer Science</subject><subject>Cricetinae</subject><subject>Cricetulus</subject><subject>Cysteine Proteinase Inhibitors - pharmacology</subject><subject>Degeneration</subject><subject>Dimethyl Sulfoxide - pharmacology</subject><subject>Experiments</subject><subject>Furans - pharmacology</subject><subject>Genetic aspects</subject><subject>Lactones - pharmacology</subject><subject>Mitochondria</subject><subject>Mitochondria - classification</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - enzymology</subject><subject>Mitochondria - ultrastructure</subject><subject>Mitochondrial DNA</subject><subject>Models, Biological</subject><subject>Nervous system</subject><subject>Oligopeptides - pharmacology</subject><subject>Pattern Recognition, Automated - statistics & numerical data</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>Studies</subject><issn>1553-7358</issn><issn>1553-734X</issn><issn>1553-7358</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNqVkk2P0zAQhiMEYpeFf4AgEgfEocUfceJckKoVH5VWIPFx4GSNHSd1ldhZO1nov2dKu6utxAX54NH4eV-PZibLnlOypLyib7dhjh765Wi0W1JCGKPsQXZOheCLigv58F58lj1JaUsIhnX5ODtjtK6lqMR59nM1T2GAyZl8CHHchD50zkCfp1lPu9H5Lo_2xkKfcm9_5TH0NuWhzQ2kERLGzueDm4LZBN9Eh8Jm52FwJj3NHrUos8-O90X248P775efFldfPq4vV1cLU9ZyWrStlFo3sqaUMdaApKJmNZbKDK2AlFwTDVDWFEqomK5FTa1mxoimqIiVll9kLw--Yx-SOnYlKcrxyFLQCon1gWgCbNUY3QBxpwI49TcRYqcgYgd6q4SktGCtqUwFBTCK_tqW0gpNQBSCode742-zHmxjrJ8i9Cempy_ebVQXbhQWIwUp0OD10SCG69mmSQ0uGdv34G2Yk5I4GCIo50i-OpAdYGXOtwENzZ5WK1YxXhac7Ata_oPC01icQvC2dZg_Ebw5ESAz2d9TB3NKav3t63-wn0_Z4sCaGFKKtr1rCiVqv7G3s1H7jVXHjUXZi_sNvRPdrij_A5Hg5-k</recordid><startdate>20111001</startdate><enddate>20111001</enddate><creator>Peng, Jyh-Ying</creator><creator>Lin, Chung-Chih</creator><creator>Chen, Yen-Jen</creator><creator>Kao, Lung-Sen</creator><creator>Liu, Young-Chau</creator><creator>Chou, Chung-Chien</creator><creator>Huang, Yi-Hung</creator><creator>Chang, Fang-Rong</creator><creator>Wu, Yang-Chang</creator><creator>Tsai, Yuh-Show</creator><creator>Hsu, Chun-Nan</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISN</scope><scope>ISR</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20111001</creationdate><title>Automatic morphological subtyping reveals new roles of caspases in mitochondrial dynamics</title><author>Peng, Jyh-Ying ; Lin, Chung-Chih ; Chen, Yen-Jen ; Kao, Lung-Sen ; Liu, Young-Chau ; Chou, Chung-Chien ; Huang, Yi-Hung ; Chang, Fang-Rong ; Wu, Yang-Chang ; Tsai, Yuh-Show ; Hsu, Chun-Nan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c698t-ff88bbd8911222da8159290032c17a063b0baa691a6a72b9591eb2cc5d470e8e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Aging</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Automation</topic><topic>Biology</topic><topic>Caspase Inhibitors</topic><topic>Caspases - metabolism</topic><topic>Cellular biology</topic><topic>Cellular signal transduction</topic><topic>CHO Cells</topic><topic>Classification</topic><topic>Computational Biology</topic><topic>Computer Science</topic><topic>Cricetinae</topic><topic>Cricetulus</topic><topic>Cysteine Proteinase Inhibitors - pharmacology</topic><topic>Degeneration</topic><topic>Dimethyl Sulfoxide - pharmacology</topic><topic>Experiments</topic><topic>Furans - pharmacology</topic><topic>Genetic aspects</topic><topic>Lactones - pharmacology</topic><topic>Mitochondria</topic><topic>Mitochondria - classification</topic><topic>Mitochondria - drug effects</topic><topic>Mitochondria - enzymology</topic><topic>Mitochondria - ultrastructure</topic><topic>Mitochondrial DNA</topic><topic>Models, Biological</topic><topic>Nervous system</topic><topic>Oligopeptides - pharmacology</topic><topic>Pattern Recognition, Automated - statistics & numerical data</topic><topic>Physiological aspects</topic><topic>Proteins</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peng, Jyh-Ying</creatorcontrib><creatorcontrib>Lin, Chung-Chih</creatorcontrib><creatorcontrib>Chen, Yen-Jen</creatorcontrib><creatorcontrib>Kao, Lung-Sen</creatorcontrib><creatorcontrib>Liu, Young-Chau</creatorcontrib><creatorcontrib>Chou, Chung-Chien</creatorcontrib><creatorcontrib>Huang, Yi-Hung</creatorcontrib><creatorcontrib>Chang, Fang-Rong</creatorcontrib><creatorcontrib>Wu, Yang-Chang</creatorcontrib><creatorcontrib>Tsai, Yuh-Show</creatorcontrib><creatorcontrib>Hsu, Chun-Nan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>PLoS computational biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peng, Jyh-Ying</au><au>Lin, Chung-Chih</au><au>Chen, Yen-Jen</au><au>Kao, Lung-Sen</au><au>Liu, Young-Chau</au><au>Chou, Chung-Chien</au><au>Huang, Yi-Hung</au><au>Chang, Fang-Rong</au><au>Wu, Yang-Chang</au><au>Tsai, Yuh-Show</au><au>Hsu, Chun-Nan</au><au>Covert, Markus W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Automatic morphological subtyping reveals new roles of caspases in mitochondrial dynamics</atitle><jtitle>PLoS computational biology</jtitle><addtitle>PLoS Comput Biol</addtitle><date>2011-10-01</date><risdate>2011</risdate><volume>7</volume><issue>10</issue><spage>e1002212</spage><epage>e1002212</epage><pages>e1002212-e1002212</pages><issn>1553-7358</issn><issn>1553-734X</issn><eissn>1553-7358</eissn><abstract>Morphological dynamics of mitochondria is associated with key cellular processes related to aging and neuronal degenerative diseases, but the lack of standard quantification of mitochondrial morphology impedes systematic investigation. This paper presents an automated system for the quantification and classification of mitochondrial morphology. We discovered six morphological subtypes of mitochondria for objective quantification of mitochondrial morphology. These six subtypes are small globules, swollen globules, straight tubules, twisted tubules, branched tubules and loops. The subtyping was derived by applying consensus clustering to a huge collection of more than 200 thousand mitochondrial images extracted from 1422 micrographs of Chinese hamster ovary (CHO) cells treated with different drugs, and was validated by evidence of functional similarity reported in the literature. Quantitative statistics of subtype compositions in cells is useful for correlating drug response and mitochondrial dynamics. Combining the quantitative results with our biochemical studies about the effects of squamocin on CHO cells reveals new roles of Caspases in the regulatory mechanisms of mitochondrial dynamics. This system is not only of value to the mitochondrial field, but also applicable to the investigation of other subcellular organelle morphology.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>21998575</pmid><doi>10.1371/journal.pcbi.1002212</doi><oa>free_for_read</oa></addata></record> |
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subjects | Aging Animals Apoptosis Automation Biology Caspase Inhibitors Caspases - metabolism Cellular biology Cellular signal transduction CHO Cells Classification Computational Biology Computer Science Cricetinae Cricetulus Cysteine Proteinase Inhibitors - pharmacology Degeneration Dimethyl Sulfoxide - pharmacology Experiments Furans - pharmacology Genetic aspects Lactones - pharmacology Mitochondria Mitochondria - classification Mitochondria - drug effects Mitochondria - enzymology Mitochondria - ultrastructure Mitochondrial DNA Models, Biological Nervous system Oligopeptides - pharmacology Pattern Recognition, Automated - statistics & numerical data Physiological aspects Proteins Studies |
title | Automatic morphological subtyping reveals new roles of caspases in mitochondrial dynamics |
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