{"citation":{"ieee":"F. Kage et al., “FMNL formins boost lamellipodial force generation,” Nature Communications, vol. 8. Nature Publishing Group, 2017.","mla":"Kage, Frieda, et al. “FMNL Formins Boost Lamellipodial Force Generation.” Nature Communications, vol. 8, 14832, Nature Publishing Group, 2017, doi:10.1038/ncomms14832.","short":"F. Kage, M. Winterhoff, V. Dimchev, J. Müller, T. Thalheim, A. Freise, S. Brühmann, J. Kollasser, J. Block, G.A. Dimchev, M. Geyer, H. Schnittler, C. Brakebusch, T. Stradal, M. Carlier, M.K. Sixt, J. Käs, J. Faix, K. Rottner, Nature Communications 8 (2017).","ama":"Kage F, Winterhoff M, Dimchev V, et al. FMNL formins boost lamellipodial force generation. Nature Communications. 2017;8. doi:10.1038/ncomms14832","ista":"Kage F, Winterhoff M, Dimchev V, Müller J, Thalheim T, Freise A, Brühmann S, Kollasser J, Block J, Dimchev GA, Geyer M, Schnittler H, Brakebusch C, Stradal T, Carlier M, Sixt MK, Käs J, Faix J, Rottner K. 2017. FMNL formins boost lamellipodial force generation. Nature Communications. 8, 14832.","apa":"Kage, F., Winterhoff, M., Dimchev, V., Müller, J., Thalheim, T., Freise, A., … Rottner, K. (2017). FMNL formins boost lamellipodial force generation. Nature Communications. Nature Publishing Group. https://doi.org/10.1038/ncomms14832","chicago":"Kage, Frieda, Moritz Winterhoff, Vanessa Dimchev, Jan Müller, Tobias Thalheim, Anika Freise, Stefan Brühmann, et al. “FMNL Formins Boost Lamellipodial Force Generation.” Nature Communications. Nature Publishing Group, 2017. https://doi.org/10.1038/ncomms14832."},"pubrep_id":"902","language":[{"iso":"eng"}],"article_number":"14832","_id":"659","doi":"10.1038/ncomms14832","publication":"Nature Communications","has_accepted_license":"1","author":[{"last_name":"Kage","first_name":"Frieda","full_name":"Kage, Frieda"},{"full_name":"Winterhoff, Moritz","last_name":"Winterhoff","first_name":"Moritz"},{"full_name":"Dimchev, Vanessa","last_name":"Dimchev","first_name":"Vanessa"},{"first_name":"Jan","last_name":"Müller","id":"AD07FDB4-0F61-11EA-8158-C4CC64CEAA8D","full_name":"Müller, Jan"},{"full_name":"Thalheim, Tobias","last_name":"Thalheim","first_name":"Tobias"},{"full_name":"Freise, Anika","first_name":"Anika","last_name":"Freise"},{"full_name":"Brühmann, Stefan","first_name":"Stefan","last_name":"Brühmann"},{"full_name":"Kollasser, Jana","last_name":"Kollasser","first_name":"Jana"},{"full_name":"Block, Jennifer","first_name":"Jennifer","last_name":"Block"},{"first_name":"Georgi A","last_name":"Dimchev","full_name":"Dimchev, Georgi A"},{"last_name":"Geyer","first_name":"Matthias","full_name":"Geyer, Matthias"},{"full_name":"Schnittler, Hams","first_name":"Hams","last_name":"Schnittler"},{"last_name":"Brakebusch","first_name":"Cord","full_name":"Brakebusch, Cord"},{"full_name":"Stradal, Theresia","last_name":"Stradal","first_name":"Theresia"},{"first_name":"Marie","last_name":"Carlier","full_name":"Carlier, Marie"},{"orcid":"0000-0002-6620-9179","last_name":"Sixt","first_name":"Michael K","id":"41E9FBEA-F248-11E8-B48F-1D18A9856A87","full_name":"Sixt, Michael K"},{"last_name":"Käs","first_name":"Josef","full_name":"Käs, Josef"},{"full_name":"Faix, Jan","last_name":"Faix","first_name":"Jan"},{"first_name":"Klemens","last_name":"Rottner","full_name":"Rottner, Klemens"}],"publication_identifier":{"issn":["20411723"]},"file_date_updated":"2020-07-14T12:47:34Z","ddc":["570"],"intvolume":" 8","publist_id":"7075","volume":8,"year":"2017","publication_status":"published","date_published":"2017-03-22T00:00:00Z","department":[{"_id":"MiSi"}],"abstract":[{"lang":"eng","text":"Migration frequently involves Rac-mediated protrusion of lamellipodia, formed by Arp2/3 complex-dependent branching thought to be crucial for force generation and stability of these networks. The formins FMNL2 and FMNL3 are Cdc42 effectors targeting to the lamellipodium tip and shown here to nucleate and elongate actin filaments with complementary activities in vitro. In migrating B16-F1 melanoma cells, both formins contribute to the velocity of lamellipodium protrusion. Loss of FMNL2/3 function in melanoma cells and fibroblasts reduces lamellipodial width, actin filament density and -bundling, without changing patterns of Arp2/3 complex incorporation. Strikingly, in melanoma cells, FMNL2/3 gene inactivation almost completely abolishes protrusion forces exerted by lamellipodia and modifies their ultrastructural organization. Consistently, CRISPR/Cas-mediated depletion of FMNL2/3 in fibroblasts reduces both migration and capability of cells to move against viscous media. Together, we conclude that force generation in lamellipodia strongly depends on FMNL formin activity, operating in addition to Arp2/3 complex-dependent filament branching."}],"file":[{"relation":"main_file","checksum":"dae30190291c3630e8102d8714a8d23e","content_type":"application/pdf","file_name":"IST-2017-902-v1+1_Kage_et_al-2017-Nature_Communications.pdf","access_level":"open_access","creator":"system","date_updated":"2020-07-14T12:47:34Z","file_id":"5072","date_created":"2018-12-12T10:14:21Z","file_size":9523746}],"license":"https://creativecommons.org/licenses/by/4.0/","type":"journal_article","day":"22","month":"03","article_processing_charge":"No","tmp":{"image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode"},"date_updated":"2021-01-12T08:08:06Z","title":"FMNL formins boost lamellipodial force generation","quality_controlled":"1","status":"public","oa":1,"oa_version":"Published Version","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","date_created":"2018-12-11T11:47:46Z","publisher":"Nature Publishing Group","scopus_import":1}