Flagellar oscillation: a commentary on proposed mechanisms
Eukaryotic flagella and cilia have a remarkably uniform internal ‘engine’ known as the ‘9+2’ axoneme. With few exceptions, the function of cilia and flagella is to beat rhythmically and set up relative motion between themselves and the liquid that surrounds them. The molecular basis of axonemal move...
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description | Eukaryotic flagella and cilia have a remarkably uniform internal ‘engine’ known as the ‘9+2’ axoneme. With few exceptions, the function of cilia and flagella is to beat rhythmically and set up relative motion between themselves and the liquid that surrounds them. The molecular basis of axonemal movement is understood in considerable detail, with the exception of the mechanism that provides its rhythmical or oscillatory quality. Some kind of repetitive ‘switching’ event is assumed to occur; there are several proposals regarding the nature of the ‘switch’ and how it might operate. Herein I first summarise all the factors known to influence the rate of the oscillation (the beating frequency). Many of these factors exert their effect through modulating the mean sliding velocity between the nine doublet microtubules of the axoneme, this velocity being the determinant of bend growth rate and bend propagation rate. Then I explain six proposed mechanisms for flagellar oscillation and review the evidence on which they are based. Finally, I attempt to derive an economical synthesis, drawing for preference on experimental research that has been minimally disruptive of the intricate structure of the axoneme. The ‘provisional synthesis' is that flagellar oscillation emerges from an effect of passive sliding direction on the dynein arms. Sliding in one direction facilitates force‐generating cycles and dynein‐to‐dynein synchronisation along a doublet; sliding in the other direction is inhibitory. The direction of the initial passive sliding normally oscillates because it is controlled hydrodynamically through the alternating direction of the propulsive thrust. However, in the absence of such regulation, there can be a perpetual, mechanical self‐triggering through a reversal of sliding direction due to the recoil of elastic structures that deform as a response to the prior active sliding. This provisional synthesis may be a useful basis for further examination of the problem. |
doi_str_mv | 10.1111/j.1469-185X.2009.00110.x |
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With few exceptions, the function of cilia and flagella is to beat rhythmically and set up relative motion between themselves and the liquid that surrounds them. The molecular basis of axonemal movement is understood in considerable detail, with the exception of the mechanism that provides its rhythmical or oscillatory quality. Some kind of repetitive ‘switching’ event is assumed to occur; there are several proposals regarding the nature of the ‘switch’ and how it might operate. Herein I first summarise all the factors known to influence the rate of the oscillation (the beating frequency). Many of these factors exert their effect through modulating the mean sliding velocity between the nine doublet microtubules of the axoneme, this velocity being the determinant of bend growth rate and bend propagation rate. Then I explain six proposed mechanisms for flagellar oscillation and review the evidence on which they are based. Finally, I attempt to derive an economical synthesis, drawing for preference on experimental research that has been minimally disruptive of the intricate structure of the axoneme. The ‘provisional synthesis' is that flagellar oscillation emerges from an effect of passive sliding direction on the dynein arms. Sliding in one direction facilitates force‐generating cycles and dynein‐to‐dynein synchronisation along a doublet; sliding in the other direction is inhibitory. The direction of the initial passive sliding normally oscillates because it is controlled hydrodynamically through the alternating direction of the propulsive thrust. However, in the absence of such regulation, there can be a perpetual, mechanical self‐triggering through a reversal of sliding direction due to the recoil of elastic structures that deform as a response to the prior active sliding. 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Journal compilation © 2009 Cambridge Philosophical Society</rights><rights>Copyright Cambridge University Press Aug 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4980-1f7d52215ca37fff371209775f7be721ad5890dbbeb159832d2b273907c22e8c3</citedby><cites>FETCH-LOGICAL-c4980-1f7d52215ca37fff371209775f7be721ad5890dbbeb159832d2b273907c22e8c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1469-185X.2009.00110.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1469-185X.2009.00110.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20002389$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Woolley, David M.</creatorcontrib><title>Flagellar oscillation: a commentary on proposed mechanisms</title><title>Biological reviews of the Cambridge Philosophical Society</title><addtitle>Biol Rev Camb Philos Soc</addtitle><description>Eukaryotic flagella and cilia have a remarkably uniform internal ‘engine’ known as the ‘9+2’ axoneme. With few exceptions, the function of cilia and flagella is to beat rhythmically and set up relative motion between themselves and the liquid that surrounds them. The molecular basis of axonemal movement is understood in considerable detail, with the exception of the mechanism that provides its rhythmical or oscillatory quality. Some kind of repetitive ‘switching’ event is assumed to occur; there are several proposals regarding the nature of the ‘switch’ and how it might operate. Herein I first summarise all the factors known to influence the rate of the oscillation (the beating frequency). Many of these factors exert their effect through modulating the mean sliding velocity between the nine doublet microtubules of the axoneme, this velocity being the determinant of bend growth rate and bend propagation rate. Then I explain six proposed mechanisms for flagellar oscillation and review the evidence on which they are based. Finally, I attempt to derive an economical synthesis, drawing for preference on experimental research that has been minimally disruptive of the intricate structure of the axoneme. The ‘provisional synthesis' is that flagellar oscillation emerges from an effect of passive sliding direction on the dynein arms. Sliding in one direction facilitates force‐generating cycles and dynein‐to‐dynein synchronisation along a doublet; sliding in the other direction is inhibitory. The direction of the initial passive sliding normally oscillates because it is controlled hydrodynamically through the alternating direction of the propulsive thrust. However, in the absence of such regulation, there can be a perpetual, mechanical self‐triggering through a reversal of sliding direction due to the recoil of elastic structures that deform as a response to the prior active sliding. This provisional synthesis may be a useful basis for further examination of the problem.</description><subject>Animals</subject><subject>axoneme</subject><subject>Biology</subject><subject>Biomechanical Phenomena</subject><subject>Cell Movement</subject><subject>Cilia - physiology</subject><subject>cilium</subject><subject>dynein</subject><subject>Dyneins - metabolism</subject><subject>Energy Metabolism</subject><subject>Eukaryotes</subject><subject>Flagella - physiology</subject><subject>flagellum</subject><subject>Molecules</subject><subject>oscillation</subject><subject>Velocity</subject><issn>1464-7931</issn><issn>1469-185X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtPwzAQhC0E4lH4CyjiwinFjziOKy5QKCCVIlB53FaO40BKEpe4Fe2_x6HQAyd88Ur7zWh2EAoI7hL_TiZdEsUyJAl_6VKMZRdj4neLDbS7Xmx-z1EoJCM7aM-5iYeiOGbbaMdrMGWJ3EW9QaleTVmqJrBOF36YFbbuBSrQtqpMPVPNMrB1MG3s1DqTBZXRb6ouXOX20VauSmcOfv4OehxcjvvX4fDu6qZ_Ngx1JBMcklxknFLCtWIiz3MmCMVSCJ6L1AhKVMYTibM0NSnhMmE0oykVTGKhKTWJZh10vPL1GT7mxs2gKpxuM9fGzh2IKJEMyyj25NEfcmLnTe3DQYwF5ZhG3EPJCtKNda4xOUybovJnAsHQtgsTaEuEtkRo24XvdmHhpYc__vO0Mtla-FunB05XwGdRmuW_jeH84ckPXh6u5IWbmcVarpp3iAUTHJ5HVzAay_g-uh3ABfsCqh2WDQ</recordid><startdate>201008</startdate><enddate>201008</enddate><creator>Woolley, David M.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><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>7QG</scope><scope>7SN</scope><scope>7SS</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>201008</creationdate><title>Flagellar oscillation: a commentary on proposed mechanisms</title><author>Woolley, David M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4980-1f7d52215ca37fff371209775f7be721ad5890dbbeb159832d2b273907c22e8c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>axoneme</topic><topic>Biology</topic><topic>Biomechanical Phenomena</topic><topic>Cell Movement</topic><topic>Cilia - physiology</topic><topic>cilium</topic><topic>dynein</topic><topic>Dyneins - metabolism</topic><topic>Energy Metabolism</topic><topic>Eukaryotes</topic><topic>Flagella - physiology</topic><topic>flagellum</topic><topic>Molecules</topic><topic>oscillation</topic><topic>Velocity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Woolley, David M.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Biological reviews of the Cambridge Philosophical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Woolley, David M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Flagellar oscillation: a commentary on proposed mechanisms</atitle><jtitle>Biological reviews of the Cambridge Philosophical Society</jtitle><addtitle>Biol Rev Camb Philos Soc</addtitle><date>2010-08</date><risdate>2010</risdate><volume>85</volume><issue>3</issue><spage>453</spage><epage>470</epage><pages>453-470</pages><issn>1464-7931</issn><eissn>1469-185X</eissn><coden>BRCPAH</coden><abstract>Eukaryotic flagella and cilia have a remarkably uniform internal ‘engine’ known as the ‘9+2’ axoneme. With few exceptions, the function of cilia and flagella is to beat rhythmically and set up relative motion between themselves and the liquid that surrounds them. The molecular basis of axonemal movement is understood in considerable detail, with the exception of the mechanism that provides its rhythmical or oscillatory quality. Some kind of repetitive ‘switching’ event is assumed to occur; there are several proposals regarding the nature of the ‘switch’ and how it might operate. Herein I first summarise all the factors known to influence the rate of the oscillation (the beating frequency). Many of these factors exert their effect through modulating the mean sliding velocity between the nine doublet microtubules of the axoneme, this velocity being the determinant of bend growth rate and bend propagation rate. Then I explain six proposed mechanisms for flagellar oscillation and review the evidence on which they are based. Finally, I attempt to derive an economical synthesis, drawing for preference on experimental research that has been minimally disruptive of the intricate structure of the axoneme. The ‘provisional synthesis' is that flagellar oscillation emerges from an effect of passive sliding direction on the dynein arms. Sliding in one direction facilitates force‐generating cycles and dynein‐to‐dynein synchronisation along a doublet; sliding in the other direction is inhibitory. The direction of the initial passive sliding normally oscillates because it is controlled hydrodynamically through the alternating direction of the propulsive thrust. However, in the absence of such regulation, there can be a perpetual, mechanical self‐triggering through a reversal of sliding direction due to the recoil of elastic structures that deform as a response to the prior active sliding. This provisional synthesis may be a useful basis for further examination of the problem.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>20002389</pmid><doi>10.1111/j.1469-185X.2009.00110.x</doi><tpages>18</tpages></addata></record> |
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subjects | Animals axoneme Biology Biomechanical Phenomena Cell Movement Cilia - physiology cilium dynein Dyneins - metabolism Energy Metabolism Eukaryotes Flagella - physiology flagellum Molecules oscillation Velocity |
title | Flagellar oscillation: a commentary on proposed mechanisms |
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