Literature DB >> 17344411

Microtubule-induced cortical cell polarity.

Sarah E Siegrist1, Chris Q Doe.   

Abstract

Most cells are polarized. Embryonic and stem cells can use their polarity to generate cell diversity by asymmetric cell division, whereas differentiated cells use their polarity to execute specific functions. For example, fibroblasts form an actin-rich leading edge required for cell migration, neurons form distinctive axonal and dendritic compartments important for directional signaling, and epithelial cells have apical and basolateral cortical domains necessary for maintaining tissue impermeability. It is well established that actin and actin-associated proteins are essential for generating molecular and morphological cell polarity, but only recently has it become accepted that microtubules can induce and/or maintain polarity. One common feature among different cell types is that microtubules can establish the position of cortical polarity, but are not required for cortical polarity per se. In this review, we discuss how different cell types utilize microtubules and microtubule-associated signaling pathways to generate cortical cell polarity, highlight common mechanisms, and discuss open questions for directing future research.

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Year:  2007        PMID: 17344411     DOI: 10.1101/gad.1511207

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  106 in total

1.  GSK3 controls axon growth via CLASP-mediated regulation of growth cone microtubules.

Authors:  Eun-Mi Hur; Byoung Dae Lee; Seong-Jin Kim; Wen-Lin Xu; Feng-Quan Zhou
Journal:  Genes Dev       Date:  2011-09-15       Impact factor: 11.361

2.  Conversion of the enzyme guanylate kinase into a mitotic-spindle orienting protein by a single mutation that inhibits GMP-induced closing.

Authors:  Christopher A Johnston; Dustin S Whitney; Brian F Volkman; Chris Q Doe; Kenneth E Prehoda
Journal:  Proc Natl Acad Sci U S A       Date:  2011-10-11       Impact factor: 11.205

3.  Cortical domain correction repositions the polarity boundary to match the cytokinesis furrow in C. elegans embryos.

Authors:  Christian Schenk; Henrik Bringmann; Anthony A Hyman; Carrie R Cowan
Journal:  Development       Date:  2010-05       Impact factor: 6.868

4.  Collective cell motion in endothelial monolayers.

Authors:  A Szabó; R Unnep; E Méhes; W O Twal; W S Argraves; Y Cao; A Czirók
Journal:  Phys Biol       Date:  2010-11-12       Impact factor: 2.583

5.  KIF17 regulates RhoA-dependent actin remodeling at epithelial cell-cell adhesions.

Authors:  Bipul R Acharya; Cedric Espenel; Fotine Libanje; Joel Raingeaud; Jessica Morgan; Fanny Jaulin; Geri Kreitzer
Journal:  J Cell Sci       Date:  2016-01-12       Impact factor: 5.285

6.  Establishing new sites of polarization by microtubules.

Authors:  Nicolas Minc; Scott V Bratman; Roshni Basu; Fred Chang
Journal:  Curr Biol       Date:  2009-01-15       Impact factor: 10.834

7.  Hepatoma-derived growth factor-related protein-3 interacts with microtubules and promotes neurite outgrowth in mouse cortical neurons.

Authors:  Heba M El-Tahir; Mekky M Abouzied; Rainer Gallitzendoerfer; Volkmar Gieselmann; Sebastian Franken
Journal:  J Biol Chem       Date:  2009-02-23       Impact factor: 5.157

8.  Dynamic microtubules and endomembrane cycling contribute to polarity establishment and early development of Ectocarpus mitospores.

Authors:  Jeffrey J Green; Diégo Cordero Cervantes; Nick T Peters; Kyle O Logan; Darryl L Kropf
Journal:  Protoplasma       Date:  2013-01-16       Impact factor: 3.356

9.  Control of endothelial cell polarity and sprouting angiogenesis by non-centrosomal microtubules.

Authors:  Maud Martin; Alexandra Veloso; Jingchao Wu; Eugene A Katrukha; Anna Akhmanova
Journal:  Elife       Date:  2018-03-16       Impact factor: 8.140

Review 10.  Random versus directionally persistent cell migration.

Authors:  Ryan J Petrie; Andrew D Doyle; Kenneth M Yamada
Journal:  Nat Rev Mol Cell Biol       Date:  2009-07-15       Impact factor: 94.444

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