نتایج جستجو برای: microtubule

تعداد نتایج: 31980  

2014
Tatjana Kleele Petar Marinković Philip R. Williams Sina Stern Emily E. Weigand Peter Engerer Ronald Naumann Jana Hartmann Rosa M. Karl Frank Bradke Derron Bishop Jochen Herms Arthur Konnerth Martin Kerschensteiner Leanne Godinho Thomas Misgeld

Microtubule dynamics in neurons play critical roles in physiology, injury and disease and determine microtubule orientation, the cell biological correlate of neurite polarization. Several microtubule binding proteins, including end-binding protein 3 (EB3), specifically bind to the growing plus tip of microtubules. In the past, fluorescently tagged end-binding proteins have revealed microtubule ...

Journal: :Developmental cell 2015
Raiko Stephan Bernd Goellner Eliza Moreno C Andrew Frank Tabea Hugenschmidt Christel Genoud Hermann Aberle Jan Pielage

The dimensions of axons and synaptic terminals determine cell-intrinsic properties of neurons; however, the cellular mechanisms selectively controlling establishment and maintenance of neuronal compartments remain poorly understood. Here, we show that two giant Drosophila Ankyrin2 isoforms, Ank2-L and Ank2-XL, and the MAP1B homolog Futsch form a membrane-associated microtubule-organizing comple...

2017
Amayra Hernández-Vega Marcus Braun Lara Scharrel Marcus Jahnel Susanne Wegmann Bradley T. Hyman Simon Alberti Stefan Diez Anthony A. Hyman

Non-centrosomal microtubule bundles play important roles in cellular organization and function. Although many diverse proteins are known that can bundle microtubules, biochemical mechanisms by which cells could locally control the nucleation and formation of microtubule bundles are understudied. Here, we demonstrate that the concentration of tubulin into a condensed, liquid-like compartment com...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2011
Sebastian P Maurer Peter Bieling Julia Cope Andreas Hoenger Thomas Surrey

Microtubule plus-end-tracking proteins (+TIPs) localize to growing microtubule plus ends to regulate a multitude of essential microtubule functions. End-binding proteins (EBs) form the core of this network by recognizing a distinct structural feature transiently existing in an extended region at growing microtubule ends and by recruiting other +TIPs to this region. The nature of the conformatio...

Journal: :Development 2017
Emmanuelle Gigant Marine Stefanutti Kimberley Laband Agata Gluszek-Kustusz Frances Edwards Benjamin Lacroix Gilliane Maton Julie C Canman Julie P I Welburn Julien Dumont

In most species, oocytes lack centrosomes. Accurate meiotic spindle assembly and chromosome segregation - essential to prevent miscarriage or developmental defects - thus occur through atypical mechanisms that are not well characterized. Using quantitative in vitro and in vivo functional assays in the C. elegans oocyte, we provide novel evidence that the kinesin-13 KLP-7 promotes destabilizatio...

2014
Bin Wang Yan-Hua Rao Makoto Inoue Rui Hao Chun-Hsiang Lai David Chen Stacey. L McDonald Moon-Chang Choi Qiu Wang Mari Shinohara Tso-Pang Yao

Reversible acetylation of α-tubulin is an evolutionarily conserved modification in microtubule networks. Despite its prevalence, the physiological function and regulation of microtubule acetylation remain poorly understood. Here we report that macrophages challenged by bacterial lipopolysaccharides (LPS) undergo extensive microtubule acetylation. Suppression of LPS-induced microtubule acetylati...

Journal: :Cell 2006
Iain M. Cheeseman Joshua S. Chappie Elizabeth M. Wilson-Kubalek Arshad Desai

The microtubule-binding interface of the kinetochore is of central importance in chromosome segregation. Although kinetochore components that stabilize, translocate on, and affect the polymerization state of microtubules have been identified, none have proven essential for kinetochore-microtubule interactions. Here, we examined the conserved KNL-1/Mis12 complex/Ndc80 complex (KMN) network, whic...

Journal: :Ageing and neurodegenerative diseases 2022

Alzheimer’s disease (AD) is a progressive neurodegenerative disorder characterized by two pathological hallmark lesions: extracellular plaques composed of ?-amyloid (A?) peptide and intracellular neurofibrillary tangles made up highly phosphorylated tau protein. Over the past decades, most disease-modifying therapies against AD have been developed mainly on basis amyloid cascade hypothesis with...

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