Tracheal motile cilia in mice require CAMSAP3 for formation of central microtubule pair and coordinated beating
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T. Shibata | M. Takeichi | Masamitsu Sato | T. Fujimori | K. Misaki | S. Yonemura | M. Toya | Yasutaka Kakui | Takahiro Ide | Takaki Yamamoto | H. Saito | Fumiko Matsukawa-Usami | Toshiya Kimura | Kenta Onoue | S. Okayama | Yurina Soba
[1] T. Abe,et al. Cyst formation in proximal renal tubules caused by dysfunction of the microtubule minus-end regulator CAMSAP3 , 2021, Scientific Reports.
[2] M. Takeichi,et al. Intercellular and intracellular cilia orientation is coordinated by CELSR1 and CAMSAP3 in oviduct multi-ciliated cells , 2021, Journal of Cell Science.
[3] M. Kawasaki,et al. CAMSAP3 is required for mTORC1-dependent ependymal cell growth and lateral ventricle shaping in mouse brains , 2020, Development.
[4] M. Cheatham,et al. CAMSAP3 facilitates basal body polarity and the formation of the central pair of microtubules in motile cilia , 2020, Proceedings of the National Academy of Sciences.
[5] Xiumin Yan,et al. Wdr47 Controls Neuronal Polarization through the Camsap Family Microtubule Minus-End-Binding Proteins. , 2020, Cell reports.
[6] D. Agard,et al. Electron cryotomography of intact motile cilia defines the basal body to axoneme transition , 2019, The Journal of cell biology.
[7] Adam C. Martin,et al. Microtubules promote intercellular contractile force transmission during tissue folding , 2019, The Journal of cell biology.
[8] A. Sagasti,et al. Patronin-mediated minus end growth is required for dendritic microtubule polarity , 2019, The Journal of cell biology.
[9] F. Yu,et al. Patronin governs minus-end-out orientation of dendritic microtubules to promote dendrite pruning in Drosophila , 2019, eLife.
[10] K. Gull,et al. Basalin is an evolutionarily unconstrained protein revealed via a conserved role in flagellum basal plate function , 2019, eLife.
[11] Xiumin Yan,et al. Rsph9 is critical for ciliary radial spoke assembly and central pair microtubule stability , 2018, Biology of the cell.
[12] T. Abe,et al. CAMSAP3 maintains neuronal polarity through regulation of microtubule stability , 2018, Proceedings of the National Academy of Sciences.
[13] Anna Akhmanova,et al. Control of endothelial cell polarity and sprouting angiogenesis by non-centrosomal microtubules , 2018, eLife.
[14] Yu-Chiun Wang,et al. A homeostatic apical microtubule network shortens cells for epithelial folding via a basal polarity shift , 2017, Nature Cell Biology.
[15] S. Dell,et al. Primary ciliary dyskinesia: mechanisms and management , 2017, The application of clinical genetics.
[16] L. Pelletier,et al. The Ciliary Transition Zone: Finding the Pieces and Assembling the Gate , 2017, Molecules and cells.
[17] S. Tsukita,et al. Three-dimensional Organization of Layered Apical Cytoskeletal Networks Associated with Mouse Airway Tissue Development , 2017, Scientific Reports.
[18] Elizabeth F. Smith,et al. The Central Apparatus of Cilia and Eukaryotic Flagella. , 2017, Cold Spring Harbor perspectives in biology.
[19] Maud Martin,et al. Control of apico–basal epithelial polarity by the microtubule minus-end-binding protein CAMSAP3 and spectraplakin ACF7 , 2016, Journal of Cell Science.
[20] K. Gull,et al. Cilium transition zone proteome reveals compartmentalization and differential dynamics of ciliopathy complexes , 2016, Proceedings of the National Academy of Sciences.
[21] D. St Johnston,et al. Patronin/Shot Cortical Foci Assemble the Noncentrosomal Microtubule Array that Specifies the Drosophila Anterior-Posterior Axis , 2016, Developmental cell.
[22] M. Kawasaki,et al. CAMSAP3 orients the apical-to-basal polarity of microtubule arrays in epithelial cells , 2015, Proceedings of the National Academy of Sciences.
[23] Duanduan Chen,et al. Absence of Radial Spokes in Mouse Node Cilia Is Required for Rotational Movement but Confers Ultrastructural Instability as a Trade-Off. , 2015, Developmental cell.
[24] R. Crystal,et al. Cilia dysfunction in lung disease. , 2015, Annual review of physiology.
[25] T. Uemura,et al. Celsr1 is required for the generation of polarity at multiple levels of the mouse oviduct , 2014, Development.
[26] K. Oegema,et al. The microtubule minus-end-binding protein patronin/PTRN-1 is required for axon regeneration in C. elegans. , 2014, Cell reports.
[27] Michael C. Burke,et al. Chibby promotes ciliary vesicle formation and basal body docking during airway cell differentiation , 2014, The Journal of cell biology.
[28] J. Wallingford,et al. Multiciliated Cells , 2014, Current Biology.
[29] D. Clare,et al. Basal foot MTOC organizes pillar MTs required for coordination of beating cilia , 2014, Nature Communications.
[30] Eugene A. Katrukha,et al. Microtubule Minus-End Binding Protein CAMSAP2 Controls Axon Specification and Dendrite Development , 2014, Neuron.
[31] P. Luther,et al. Characterizing the ultrastructure of primary ciliary dyskinesia transposition defect using electron tomography , 2014, Cytoskeleton.
[32] Melissa C. Hendershott,et al. Regulation of microtubule minus-end dynamics by CAMSAPs and Patronin , 2014, Proceedings of the National Academy of Sciences.
[33] M. Goodman,et al. PTRN-1, a microtubule minus end-binding CAMSAP homolog, promotes microtubule function in Caenorhabditis elegans neurons , 2014, eLife.
[34] C. Hoogenraad,et al. Microtubule minus-end stabilization by polymerization-driven CAMSAP deposition. , 2014, Developmental cell.
[35] J. McIntosh,et al. Modes of flagellar assembly in Chlamydomonas reinhardtii and Trypanosoma brucei , 2014, eLife.
[36] S. Tsukita,et al. Two appendages homologous between basal bodies and centrioles are formed using distinct Odf2 domains , 2013, The Journal of cell biology.
[37] P. Chuang,et al. Fused (Stk36) is a ciliary protein required for central pair assembly and motile cilia orientation in the mammalian oviduct , 2013, Developmental dynamics : an official publication of the American Association of Anatomists.
[38] P. Bignone,et al. A conserved sequence in calmodulin regulated spectrin-associated protein 1 links its interaction with spectrin and calmodulin to neurite outgrowth , 2013, Journal of neurochemistry.
[39] B. Housset,et al. Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects. , 2013, American journal of human genetics.
[40] M. Takeichi,et al. Nezha/CAMSAP3 and CAMSAP2 cooperate in epithelial-specific organization of noncentrosomal microtubules , 2012, Proceedings of the National Academy of Sciences.
[41] B. Durand,et al. Drosophila chibby is required for basal body formation and ciliogenesis but not for Wg signaling , 2012, The Journal of cell biology.
[42] J. Shah,et al. The ciliary transition zone: from morphology and molecules to medicine. , 2012, Trends in cell biology.
[43] T. Noda,et al. Coordinated Ciliary Beating Requires Odf2-Mediated Polarization of Basal Bodies via Basal Feet , 2012, Cell.
[44] Lance Lee. Mechanisms of mammalian ciliary motility: Insights from primary ciliary dyskinesia genetics. , 2011, Gene.
[45] Sarah S. Goodwin,et al. Patronin Regulates the Microtubule Network by Protecting Microtubule Minus Ends , 2010, Cell.
[46] K. Sawamoto,et al. Coupling between hydrodynamic forces and planar cell polarity orients mammalian motile cilia , 2010, Nature Cell Biology.
[47] P. Bignone,et al. The CKK domain (DUF1781) binds microtubules and defines the CAMSAP/ssp4 family of animal proteins. , 2009, Molecular biology and evolution.
[48] Jau-Nian Chen,et al. Fused has evolved divergent roles in vertebrate Hedgehog signalling and motile ciliogenesis , 2009, Nature.
[49] M. Takeichi,et al. Anchorage of Microtubule Minus Ends to Adherens Junctions Regulates Epithelial Cell-Cell Contacts , 2008, Cell.
[50] M. Sanderson,et al. Mutations in Hydin impair ciliary motility in mice , 2008, The Journal of cell biology.
[51] K. Gull,et al. The hydrocephalus inducing gene product, Hydin, positions axonemal central pair microtubules , 2007, BMC Biology.
[52] P. Satir,et al. Overview of structure and function of mammalian cilia. , 2007, Annual review of physiology.
[53] S. Hell,et al. 2,2′‐Thiodiethanol: A new water soluble mounting medium for high resolution optical microscopy , 2007, Microscopy research and technique.
[54] Keith Gull,et al. Centriole/basal body morphogenesis and migration during ciliogenesis in animal cells , 2006, Journal of Cell Science.
[55] Joseph G. Gleeson,et al. Transgenic Mouse Line with Green-fluorescent Protein-labeled Centrin 2 allows Visualization of the Centrosome in Living Cells , 2004, Transgenic Research.
[56] C. O’Callaghan,et al. Central microtubular agenesis causing primary ciliary dyskinesia. , 2004, American journal of respiratory and critical care medicine.
[57] F. Rodríguez de Castro,et al. Absence of Central Microtubules and Transposition in the Ciliary Apparatus of Three Siblings , 2000, Respiration.
[58] A. Bretscher,et al. Ezrin is concentrated in the apical microvilli of a wide variety of epithelial cells whereas moesin is found primarily in endothelial cells. , 1993, Journal of cell science.
[59] C. Kung,et al. Ultrastructure of the proximal region of somatic cilia in Paramecium tetraurelia , 1978, The Journal of cell biology.
[60] N. Gilula,et al. THE CILIARY NECKLACE , 1972, The Journal of cell biology.
[61] J. Tucker. Development and deployment of cilia, basal bodies, and other microtubular organelles in the cortex of the ciliate Nassula. , 1971, Journal of cell science.
[62] Pinfen Yang,et al. The radial spokes and central apparatus: mechano-chemical transducers that regulate flagellar motility. , 2004, Cell motility and the cytoskeleton.
[63] T. Aoki,et al. Localization of gamma-tubulin to the basal foot associated with the basal body extending a cilium. , 2000, The Histochemical journal.
[64] J. McIntosh,et al. Polarity of some motility-related microtubules. , 1981, Proceedings of the National Academy of Sciences of the United States of America.