4.5 Article

QUANTITATIVE ANALYSIS OF THE EXPRESSION OF THE GLUTAMATE-ASPARTATE TRANSPORTER AND IDENTIFICATION OF FUNCTIONAL GLUTAMATE UPTAKE REVEAL A ROLE FOR COCHLEAR FIBROCYTES IN GLUTAMATE HOMEOSTASIS

期刊

NEUROSCIENCE
卷 162, 期 4, 页码 1307-1321

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2009.05.036

关键词

-

资金

  1. Deafness Research UK
  2. Royal Society University

向作者/读者索取更多资源

There are several subtypes of fibrocyte in the spiral ligament and spiral limbus of the cochlea that may contribute to fluid homeostasis. Immunocytochemical data suggest that these fibrocytes possess the glutamate-aspartate transporter, GLAST, as do supporting cells around the hair cells. However, functional glutamate uptake has not been demonstrated in fibrocytes. We used confocal and post-embedding immunogold electron microscopy to confirm that GLAST is expressed in adult fibrocytes of CD-1 mice with a relative expression: spiral limbus fibrocytes>type II>V>IV>I spiral ligament fibrocytes. Because they were sparsely present in most samples, type III fibrocytes were assessed only in one sample where their GLAST levels were similar to type I. Type II, type V and spiral limbus fibrocytes have many fine cellular processes that increase their surface area, those of the latter two coming into direct contact with perilymph, and type V fibrocytes contain the most glutamate. These data imply that glutamate uptake occurs in the fibrocytes. We assessed uptake Of D-aspartate (a glutamate analogue) together with GLAST expression immunocytochemically and electrophysiologically. D-Aspartate accumulated into GLAST expressing fibrocytes in vitro and evoked currents blockable by the GLAST inhibitor D,L-threo-beta-benzyloxyaspartate (TBOA), similar to those of supporting cells around inner hair cells. Currents were strongest in spiral limbus fibrocytes, progressively lower in type V and type II fibrocytes, and were negligible in type I fibrocytes in accordance with the relative expression levels of GLAST. We conclude that in addition to their known homeostatic functions, fibrocytes, in particular spiral limbus, type II and type V fibrocytes play a role in glutamate homeostasis in the cochlea. (C) 2009 IBRO. Published by Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Medicine, Research & Experimental

The timing of auditory sensory deficits in Norrie disease has implications for intervention

Dale Bryant, Valda Pauzuolyte, Neil J. Ingham, Aara Patel, Waheeda Pagarkar, Lucy A. Anderson, Katie E. Smith, Dale A. Moulding, Yeh C. Leong, Daniyal J. Jafree, David A. Long, Amina Al-Yassin, Karen P. Steel, Daniel J. Jagger, Andrew Forge, Wolfgang Berger, Jane C. Sowden, Maria Bitner-Glindzicz

Summary: This study reveals the sequence of physiological changes leading to hearing loss in Norrie disease and suggests early intervention is necessary to prevent hearing loss.

JCI INSIGHT (2022)

Article Biochemistry & Molecular Biology

Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease

Marilena Elpidorou, James A. Poulter, Katarzyna Szymanska, Wia Baron, Katrin Junger, Karsten Boldt, Marius Ueffing, Lydia Green, John H. Livingston, Eammon G. Sheridan, Colin A. Johnson

Summary: This study found that a mutation in the MAL gene can cause a hypomyelinating leukodystrophy similar to Pelizaeus-Merzbacher disease. The mutant MAL gene affects the distribution of PLP1, leading to abnormal development of cerebral white matter.

EUROPEAN JOURNAL OF HUMAN GENETICS (2022)

Article Oncology

Activation of autophagy reverses progressive and deleterious protein aggregation in PRPF31 patient-induced pluripotent stem cell-derived retinal pigment epithelium cells

Maria Georgiou, Chunbo Yang, Robert Atkinson, Kuan-Ting Pan, Adriana Buskin, Marina Moya Molina, Joseph Collin, Jumana Al-Aama, Franziska Goertler, Sebastian E. J. Ludwig, Tracey Davey, Reinhard Luhrmann, Sushma Nagaraja-Grellscheid, Colin A. Johnson, Robin Ali, Lyle Armstrong, Viktor Korolchuk, Henning Urlaub, Sina Mozaffari-Jovin, Majlinda Lako

Summary: Mutations in PRPF31, a core protein of the spliceosomal tri-snRNP complex, cause autosomal-dominant retinitis pigmentosa (adRP). This study used iPSC technology to generate retinal organoids and RPE models from PRPF31-adRP patients, and found that RNA splicing, autophagy and lysosome, and visual cycle pathways were significantly affected. The accumulation of cytoplasmic aggregates and impaired waste disposal mechanisms were also observed in patient-derived cells. Activation of the autophagy pathway reduced the aggregates and improved cell survival.

CLINICAL AND TRANSLATIONAL MEDICINE (2022)

Article Genetics & Heredity

Uncovering the burden of hidden ciliopathies in the 100 000 Genomes Project: a reverse phenotyping approach

Sunayna Best, Jing Yu, Jenny Lord, Matthew Roche, Christopher Mark Watson, Roel P. J. Bevers, Alex Stuckey, Savita Madhusudhan, Rosalyn Jewell, Sanjay M. Sisodiya, Siying Lin, Stephen Turner, Hannah Robinson, Joseph S. Leslie, Emma Baple, Carmel Toomes, Chris Inglehearn, Gabrielle Wheway, Colin A. Johnson

Summary: Reverse phenotyping improves the rate of successful molecular diagnosis for patients with primary ciliopathies. Previous analyses may have missed these diagnoses due to incomplete clinical data, highlighting the importance of better phenotyping for accurate diagnosis and improved patient outcomes.

JOURNAL OF MEDICAL GENETICS (2022)

Article Clinical Neurology

Inhibition of YAP/TAZ-driven TEAD activity prevents growth of NF2-null schwannoma and meningioma

Liyam Laraba, Lily Hillson, Julio Grimm de Guibert, Amy Hewitt, Maisie R. Jaques, Tracy T. Tang, Leonard Post, Emanuela Ercolano, Ganesha Rai, Shyh-Ming Yang, Daniel J. Jagger, Waldemar Woznica, Philip Edwards, Aditya G. Shivane, C. Oliver Hanemann, David B. Parkinson

Summary: The study reports new roles for the Hippo signalling pathway in NF2-null meningioma and schwannoma, and identifies the cancer stem cell marker ALDH1A1 as a target of Hippo signalling. The novel TEAD inhibitor used in the study effectively blocks the growth of these tumour types, providing potential clinical applications.
Article Audiology & Speech-Language Pathology

Structural changes in the human stria vascularis induced by aminoglycosides and loop diuretics

Anthony Wright, Andrew Forge, Daniel J. Jagger

Summary: The human stria vascularis was examined in individuals who had received loop diuretics, aminoglycoside antibiotics, or a combination of the two. Structural changes were observed in the stria vascularis, which were similar to those seen in animal models. The study highlights the importance of using animal models to predict human ototoxicity.

HEARING RESEARCH (2022)

Article Engineering, Biomedical

From mesenchymal niches to engineered in vitro model systems: Exploring and exploiting biomechanical regulation of vertebrate hedgehog signalling

Fatmah I. Ghuloum, Colin A. Johnson, Natalia A. Riobo-Del Galdo, Mahetab H. Amer

Summary: This review provides an overview of the role of Hedgehog signalling and mechanobiology in bone development and regeneration, highlighting the importance of Hedgehog signalling pathway response to mechanical cues in bone marrow-derived mesenchymal stromal cells and osteogenesis. Different tissue engineering strategies are proposed to apply the knowledge of 3D material-cell interactions in the modulation of Hedgehog signalling for research applications.

MATERIALS TODAY BIO (2022)

Article Multidisciplinary Sciences

The SHDRA syndrome-associated gene TMEM260 encodes a protein-specific O-mannosyltransferase

Ida Signe Bohse Larsen, Lorenzo Povolo, Luping Zhou, Weihua Tian, Kasper Johansen Mygind, John Hintze, Chen Jiang, Verity Hartill, Katrina Prescott, Colin A. Johnson, Sureni V. Mullegama, Allyn McConkie-Rosell, Marie McDonald, Lars Hansen, Sergey Y. Vakhrushev, Katrine T. Schjoldager, Henrik Clausen, Thomas Worzfeld, Hiren J. Joshi, Adnan Halim

Summary: Mutations in the TMEM260 gene cause heart defects and renal anomalies syndrome. The TMEM260 gene encodes an ER-located protein O-mannosyltransferase that selectively glycosylates IPT domains. Disease-causing TMEM260 mutations impair O-mannosylation of IPT domains and result in receptor matura-tion defects and abnormal growth of 3D cell models.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2023)

Article Genetics & Heredity

Racgap1 knockdown results in cells with multiple cilia due to cytokinesis failure

Basudha Basu, Alice V. R. Lake, Becky China, Katarzyna Szymanska, Gabrielle Wheway, Sandra Bell, Ewan Morrison, Jacquelyn Bond, Colin A. Johnson

Summary: This study re-analyzed a genetic screen to identify the mechanisms behind aberrant formation of supernumerary primary cilia in mammalian cells. RACGAP1 was identified as the strongest candidate hit. The results showed that cytokinesis failure led to the formation of supernumerary cilia, and this has functional implications in diseases marked by centrosomal amplification.

ANNALS OF HUMAN GENETICS (2023)

Article Neurosciences

Age-related changes in P2Y receptor signalling in mouse cochlear supporting cells

Sarah A. Hool, Jing-Yi Jeng, Daniel J. Jagger, Walter Marcotti, Federico Ceriani

Summary: This study investigated the changes in metabolism-related purinergic receptors in the supporting cells of the cochlea during aging. It was found that the expression of P2Y(2) and P2Y(4) receptors increased in the aged cochlea, leading to larger calcium responses and calcium oscillations. These findings may contribute to a better understanding of age-related hearing loss.

JOURNAL OF PHYSIOLOGY-LONDON (2023)

Article Materials Science, Biomaterials

Towards modular engineering of cell signalling: Topographically-textured microparticles induce osteogenesis via activation of canonical hedgehog signalling

Fatmah I. Ghuloum, Lee A. Stevens, Colin A. Johnson, Natalia A. Riobo-Del Galdo, Mahetab H. Amer

Summary: This study proposes a mechanism linking the activation of Hedgehog signalling to the osteoinductive effect of surface-engineered, topographically-textured polymeric microparticles. The researchers found that the topographical microenvironment plays a role in modulating Hedgehog signalling and inducing osteogenesis in mesenchymal stem cells. This study highlights the potential for tailoring substrate topographical design to offer cell-instructive 3D microenvironments.

BIOMATERIALS ADVANCES (2023)

Meeting Abstract Ophthalmology

Activation of autophagy reverses progressive and deleterious protein aggregation in PRPF31 patient induced pluripotent stem cells (iPSCs)-derived retinal pigment epithelium (RPE) cells

Maria Georgiou, Chunbo Yang, Robert Atkinson, Kuan-Ting Pan, Adriana Buskin, Marina Moya Molina, Joseph Collin, Sebastian E. J. Ludwig, Sushma Nagaraja-Grellscheid, Colin Johnson, Robin Ali, Lyle Armstrong, Viktor Korolchuk, Henning Urlaub, Sina Mozaffari-Jovin, Majlinda Lako

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2022)

Meeting Abstract Ophthalmology

Elucidating the Mechanism of PRPF-linked Retinitis Pigmentosa

Rob Atkinson, Chunbo Yang, Katarzyna Szymanska, Maria Georgiou, Chia Beh, Joseph Collin, Marina Moya Molina, Ross Laws, Sina Mozaffari-Jovin, Colin Johnson, Majlinda Lako

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2022)

Article Biochemistry & Molecular Biology

Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia

Evangelia S. Panagiotou, Narcis Fernandez-Fuentes, Layal Abi Farraj, Martin McKibbin, Nursel H. Elcioglu, Hussain Jafri, Eren Cerman, David A. Parry, Clare V. Logan, Colin A. Johnson, Chris F. Inglehearn, Carmel Toomes, Manir Ali

Summary: This study aimed to investigate the molecular basis of recessively inherited congenital cataract, microcornea, and corneal opacification. Through analysis using methods such as autozygosity mapping and whole-exome sequencing, mutations in the SIX6 gene were found to be associated with the occurrence of ocular diseases.

MOLECULAR VISION (2022)

Article Pediatrics

Orthopaedic Aspects of SAMS Syndrome

Dirk E. Schrander, Heleen M. Staal, Colin A. Johnson, Alistair Calder, Neeti Ghali, Albert E. Chudley, Constance T. R. M. Stumpel

Summary: SAMS syndrome is an ultra-rare developmental disorder characterized by short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities. Only four affected individuals have been reported to date. The syndrome includes orthopaedic diagnoses such as scapulohumoral synostosis and bilateral congenital ventral dislocation of the hips. Therefore, SAMS syndrome should be considered as the primary diagnosis when bilateral congenital ventral dislocation of the hips and/or scapulohumoral synostosis are found or suspected.

JOURNAL OF PEDIATRIC GENETICS (2022)

Article Neurosciences

Human Placenta Derived Mesenchymal Stem Cells Transplantation Reducing Cellular Apoptosis in Hypoxic-Ischemic Neonatal Rats by Down-Regulating Semaphorin 3A/Neuropilin-1

Yang He, Jun Tang, Meng Zhang, Junjie Ying, Dezhi Mu

Summary: This study investigated the protective effects and mechanisms of human placenta derived mesenchymal stem cells (hPMSCs) transplantation in a rat model of hypoxic-ischemic encephalopathy (HIE). The results showed that hPMSCs transplantation reduced apoptosis and improved long-term neurological prognosis. Furthermore, the downregulation of Sema 3A/NRP-1 expression and activation of the PI3K/Akt/mTOR signaling pathway played a key role in the protective effects of hPMSCs.

NEUROSCIENCE (2024)

Article Neurosciences

Probing the Neurophysiology of Temporal Sensitivity in the Somatosensory System Using the Mismatch Negativity (MMN) Sensory Memory Paradigm

Emily L. Isenstein, Edward G. Freedman, Jiayi Xu, Ian A. DeAndrea-Lazarus, John J. Foxe

Summary: This study evaluated electrophysiological discrimination of parametric somatosensory stimuli in healthy young adults to understand how the brain processes the duration of tactile information. The results showed that participants did not electrophysiologically discriminate between 100 and 115 ms, but they exhibited distinct electrophysiological responses when the deviant stimuli were 130, 145, and 160 ms. These findings contribute to a better understanding of tactile sensitivity in different clinical conditions.

NEUROSCIENCE (2024)

Article Neurosciences

Enhancement of the Evoked Excitatory Transmission in the Nucleus Tractus Solitarius Neurons after Sustained Hypoxia in Mice Depends on A2A Receptors

Juliana R. Souza, Ludmila Lima-Silveira, Daniela Accorsi-Mendonca, Benedito H. Machado

Summary: This study demonstrates that A2A receptors play a crucial role in modulating synaptic transmission in the NTS neurons and are required for the enhancement of glutamatergic transmission observed under short-term sustained hypoxia conditions.

NEUROSCIENCE (2024)

Article Neurosciences

Correlation Between Cued Fear Memory Retrieval and Oscillatory Network Inhibition in the Amygdala Is Disrupted by Acute REM Sleep Deprivation

Miki Hashizume, Rina Ito, Rie Suge, Yasushi Hojo, Gen Murakami, Takayuki Murakoshi

Summary: The basolateral amygdaloid complex (BLA) is closely involved in the formation of emotional memories, including both aversive memory and contextual fear memory. Acute sleep deprivation (SD) disrupts the acquisition of tone-associated fear memory in juvenile rats, but has no significant effect on contextual fear memory. Slow network oscillation in the amygdala contributes to the formation of amygdala-dependent fear memory in relation to sleep.

NEUROSCIENCE (2024)

Article Neurosciences

Enhanced Gasdermin-E-mediated Pyroptosis in Alzheimer's Disease

Qunxian Wang, Shipeng Guo, Dongjie Hu, Xiangjun Dong, Zijun Meng, Yanshuang Jiang, Zijuan Feng, Weihui Zhou, Weihong Song

Summary: GSDME plays a crucial role in the pathogenesis of Alzheimer's disease by regulating the switch from apoptosis to pyroptosis and participating in neuroinflammatory response. Knockdown of GSDME has been shown to improve cognitive impairments, indicating that GSDME could be a therapeutic target for Alzheimer's disease.

NEUROSCIENCE (2024)