نتایج جستجو برای: stereocilia

تعداد نتایج: 641  

Journal: :PLoS ONE 2008
Sokol V. Todi Elena Sivan-Loukianova Julie S. Jacobs Daniel P. Kiehart Daniel F. Eberl

BACKGROUND Myosin VIIA (MyoVIIA) is an unconventional myosin necessary for vertebrate audition [1]-[5]. Human auditory transduction occurs in sensory hair cells with a staircase-like arrangement of apical protrusions called stereocilia. In these hair cells, MyoVIIA maintains stereocilia organization [6]. Severe mutations in the Drosophila MyoVIIA orthologue, crinkled (ck), are semi-lethal [7] a...

Journal: :Journal of molecular biology 2006
D Yan F Li M L Hall C Sage W-H Hu Cosmas Giallourakis G Upadhyay X M Ouyang L L Du John R Bethea Z Y Chen V Yajnik X Z Liu

The driving forces for the regulation of cell morphology are the Rho family GTPases that coordinate the assembly of the actin cytoskeleton. This dynamic feature is a result of tight coupling between the cytoskeleton and signal transduction and is facilitated by actin-binding proteins (ABPs). Mutations in the actin bundling and PDZ domain-containing protein harmonin are the causes of Usher syndr...

2015
Qian Wu Guo-Peng Wang Jing Xie Jing-Ying Guo Shu-Sheng Gong Jonathan I. Matsui

Tumor necrosis factor (TNF)-α is a cytokine involved in acute inflammatory phase reactions, and is the primary upstream mediator in the cochlear inflammatory response. Treatment of the organ of Corti with TNF-α can induce hair cell damage. However, the resulting morphological changes have not been systematically examined. In the present study, cochlear organotypic cultures from neonatal mice we...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2012
Richard J Goodyear Sherri M Jones Louise Sharifi Andy Forge Guy P Richardson

Recent studies have shown that mutations in PTPRQ, a gene encoding a receptor-like inositol lipid phosphatase, cause recessive, nonsyndromic, hereditary hearing loss with associated vestibular dysfunction. Although null mutations in Ptprq cause the loss of high-frequency auditory hair cells and deafness in mice, a loss of vestibular hair cells and overt behavioral defects characteristic of vest...

Journal: :Current Biology 2012
Raymond C. Merritt Uri Manor Felipe T. Salles M'hamed Grati Andrea C. Dose William C. Unrath Omar A. Quintero Christopher M. Yengo Bechara Kachar

Myosin IIIA (MYO3A) targets actin protrusion tips using a motility mechanism dependent on both motor and tail actin-binding activity [1]. We show that myosin IIIB (MYO3B) lacks tail actin-binding activity and is unable to target COS7 cell filopodia tips, yet is somehow able to target stereocilia tips. Strikingly, when MYO3B is coexpressed with espin-1 (ESPN1), a MYO3A cargo protein endogenously...

2016
Katsuki Niwa Kunio Mizutari Toshiyasu Matsui Takaomi Kurioka Takeshi Matsunobu Satoko Kawauchi Yasushi Satoh Shunichi Sato Akihiro Shiotani Yasushi Kobayashi

The ear is the organ that is most sensitive to blast overpressure, and ear damage is most frequently seen after blast exposure. Blast overpressure to the ear results in sensorineural hearing loss, which is untreatable and is often associated with a decline in the quality of life. In this study, we used a rat model to demonstrate the pathophysiological and structural changes in the inner ear tha...

Journal: :Human molecular genetics 2003
I Jill Karolyi Frank J Probst Lisa Beyer Hana Odeh Gary Dootz Kelly B Cha Donna M Martin Karen B Avraham David Kohrman David F Dolan Yehoash Raphael Sally A Camper

The unconventional myosin genes Myo15, Myo6 and Myo7a are essential for hearing in both humans and mice. Despite the expression of each gene in multiple organs, mutations result in identifiable phenotypes only in auditory or ocular sensory organs. The pirouette (pi) mouse also exhibits deafness and an inner ear pathology resembling that of Myo15 mutant mice and thus may be functionally related ...

Journal: :Journal of cell science 2014
Takehiko Ueyama Hirofumi Sakaguchi Takashi Nakamura Akihiro Goto Shigefumi Morioka Aya Shimizu Kazuki Nakao Yoshitaka Hishikawa Yuzuru Ninoyu Hidetoshi Kassai Shiro Suetsugu Takehiko Koji Bernd Fritzsch Shigenobu Yonemura Yasuo Hisa Michiyuki Matsuda Atsu Aiba Naoaki Saito

Cdc42 is a key regulator of dynamic actin organization. However, little is known about how Cdc42-dependent actin regulation influences steady-state actin structures in differentiated epithelia. We employed inner ear hair-cell-specific conditional knockout to analyze the role of Cdc42 in hair cells possessing highly elaborate stable actin protrusions (stereocilia). Hair cells of Atoh1-Cre;Cdc42(...

Journal: :The Journal of Cell Biology 1991
D Drenckhahn K Engel D Höfer C Merte L Tilney M Tilney

The apex of hair cells of the chicken auditory organ contains three different kinds of assemblies of actin filaments in close spatial proximity. These are (a) paracrystals of actin filaments with identical polarity in stereocilia, (b) a dense gellike meshwork of actin filaments forming the cuticular plate, and (c) a bundle of parallel actin filaments with mixed polarities that constitute the ci...

2008
Hwanglyong Kim Meejung Ahn Changjong Moon Seungjoon Kim Youngheun Jee Hong-Gu Joo Taekyun Shin

Galectin-3, a member of the beta-galactoside-binding protein family, has been implicated in mammalian sperm maturation. We examined galectin-3 expression in the testis and epididymis of sexually mature and immature bulls. Western blot analysis showed varying levels of galectin-3 in the bull testis and epididymis, and galectin-3 immunoreactivity was higher in the mature testis and epididymis tha...

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