The role of actin and myosin in PtK2 spindle length changes induced by laser microbeam irradiations across the spindle

dc.contributor.authorForer, Arthur
dc.contributor.authorBerns, Michael
dc.contributor.authorShah, Jagesh
dc.contributor.authorLiaw, Lih-Huei
dc.contributor.authorGomez, Veronica
dc.contributor.authorBaker, Norman
dc.contributor.authorSheykhani, Rozhan
dc.date.accessioned2021-02-22T18:00:04Z
dc.date.available2021-02-22T18:00:04Z
dc.date.issued2013-05
dc.description.abstractThis study investigates spindle biomechanical properties to better understand how spindles function. In this report, laser microbeam cutting across mitotic spindles resulted in movement of spindle poles toward the spindle equator. The pole on the cut side moved first, the other pole moved later, resulting in a shorter but symmetric spindle. Intervening spindle microtubules bent and buckled during the equatorial movement of the poles. Because of this and because there were no detectable microtubules within the ablation zone, other cytoskeletal elements would seem to be involved in the equatorial movement of the poles. One possibility is actin and myosin since pharmacological poisoning of the actin-myosin system altered the equatorial movements of both irradiated and un-irradiated poles. Immunofluorescence microscopy confirmed that actin, myosin and mono-phosphorylated myosin are associated with spindle fibres and showed that some actin and mono-phosphorylated myosin remained in the irradiated regions. Overall, our experiments suggest that actin, myosin and microtubules interact to control spindle length. We suggest that actin and myosin, possibly in conjunction with the spindle matrix, cause the irradiated pole to move toward the equator and that cross-talk between the two half spindles causes the un-irradiated pole to move toward the equator until a balanced length is obtained.en_US
dc.identifier.citationCytoskeleton (Hoboken). 2013 May;70(5):241-59.en_US
dc.identifier.issn1949-3584
dc.identifier.urihttps://doi.org/10.1002/cm.21104en_US
dc.identifier.urihttp://hdl.handle.net/10315/38108
dc.language.isoenen_US
dc.publisherWileyen_US
dc.rightsWiley This is the peer reviewed version of the following article: [Cytoskeleton (Hoboken). 2013 May;70(5):241-59.], which has been published in final form at [https://doi.org/10.1002/cm.21104]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.en_US
dc.rightsAttribution-NoDerivatives 4.0 International*
dc.rights.articlehttps://pubmed.ncbi.nlm.nih.gov/23475753/en_US
dc.rights.journalhttps://www.ncbi.nlm.nih.gov/en_US
dc.rights.publisherhttps://onlinelibrary.wiley.com/en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nd/4.0/*
dc.subjectspindle organizationen_US
dc.subjectactomyosinen_US
dc.subjectmono-phosphorylated myosinen_US
dc.subjectmicrotubule ablationen_US
dc.subjectspindle matrixen_US
dc.titleThe role of actin and myosin in PtK2 spindle length changes induced by laser microbeam irradiations across the spindleen_US
dc.title.alternativeActin and myosin in spindle length controlen_US
dc.typeArticleen_US

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