Literature DB >> 32039504

Mechanisms underlying auditory processing deficits in Fragile X syndrome.

Elizabeth A McCullagh1,2, Sarah E Rotschafer3,4, Benjamin D Auerbach5, Achim Klug1, Leonard K Kaczmarek6, Karina S Cramer3, Randy J Kulesza7, Khaleel A Razak8, Jonathan W Lovelace8, Yong Lu9, Ursula Koch10, Yuan Wang11.   

Abstract

Autism spectrum disorders (ASD) are strongly associated with auditory hypersensitivity or hyperacusis (difficulty tolerating sounds). Fragile X syndrome (FXS), the most common monogenetic cause of ASD, has emerged as a powerful gateway for exploring underlying mechanisms of hyperacusis and auditory dysfunction in ASD. This review discusses examples of disruption of the auditory pathways in FXS at molecular, synaptic, and circuit levels in animal models as well as in FXS individuals. These examples highlight the involvement of multiple mechanisms, from aberrant synaptic development and ion channel deregulation of auditory brainstem circuits, to impaired neuronal plasticity and network hyperexcitability in the auditory cortex. Though a relatively new area of research, recent discoveries have increased interest in auditory dysfunction and mechanisms underlying hyperacusis in this disorder. This rapidly growing body of data has yielded novel research directions addressing critical questions regarding the timing and possible outcomes of human therapies for auditory dysfunction in ASD.
© 2020 Federation of American Societies for Experimental Biology.

Entities:  

Keywords:  Fragile X syndrome; auditory system; autism spectrum disorders; circuit development; hyperacusis; synaptic transmission

Mesh:

Year:  2020        PMID: 32039504      PMCID: PMC7347277          DOI: 10.1096/fj.201902435R

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  166 in total

1.  Postsynaptic FMRP Regulates Synaptogenesis In Vivo in the Developing Cochlear Nucleus.

Authors:  Xiaoyu Wang; Diego A R Zorio; Leslayann Schecterson; Yong Lu; Yuan Wang
Journal:  J Neurosci       Date:  2018-06-27       Impact factor: 6.167

2.  Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures.

Authors:  Leila K Myrick; Pan-Yue Deng; Hideharu Hashimoto; Young Mi Oh; Yongcheol Cho; Mickael J Poidevin; Joshua A Suhl; Jeannie Visootsak; Valeria Cavalli; Peng Jin; Xiaodong Cheng; Stephen T Warren; Vitaly A Klyachko
Journal:  Proc Natl Acad Sci U S A       Date:  2015-01-05       Impact factor: 11.205

3.  A non-canonical pathway from cochlea to brain signals tissue-damaging noise.

Authors:  Emma N Flores; Anne Duggan; Thomas Madathany; Ann K Hogan; Freddie G Márquez; Gagan Kumar; Rebecca P Seal; Robert H Edwards; M Charles Liberman; Jaime García-Añoveros
Journal:  Curr Biol       Date:  2015-01-29       Impact factor: 10.834

4.  Fragile X mental retardation protein is required for rapid experience-dependent regulation of the potassium channel Kv3.1b.

Authors:  John G Strumbos; Maile R Brown; Jack Kronengold; Daniel B Polley; Leonard K Kaczmarek
Journal:  J Neurosci       Date:  2010-08-04       Impact factor: 6.167

5.  Altered synaptic plasticity in a mouse model of fragile X mental retardation.

Authors:  Kimberly M Huber; Sean M Gallagher; Stephen T Warren; Mark F Bear
Journal:  Proc Natl Acad Sci U S A       Date:  2002-05-28       Impact factor: 11.205

6.  Seizures in fragile X syndrome: characteristics and comorbid diagnoses.

Authors:  Elizabeth Berry-Kravis; Melissa Raspa; Lisa Loggin-Hester; Ellen Bishop; David Holiday; Donald B Bailey
Journal:  Am J Intellect Dev Disabil       Date:  2010-11

Review 7.  The translation of translational control by FMRP: therapeutic targets for FXS.

Authors:  Jennifer C Darnell; Eric Klann
Journal:  Nat Neurosci       Date:  2013-04-14       Impact factor: 24.884

8.  Recurrent otitis media in the fragile X syndrome.

Authors:  R J Hagerman; D Altshul-Stark; P McBogg
Journal:  Am J Dis Child       Date:  1987-02

9.  Somatosensory cortical barrel dendritic abnormalities in a mouse model of the fragile X mental retardation syndrome.

Authors:  Roberto Galvez; Anjali R Gopal; William T Greenough
Journal:  Brain Res       Date:  2003-05-02       Impact factor: 3.252

10.  Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by the small-molecule PAK inhibitor FRAX486.

Authors:  Bridget M Dolan; Sergio G Duron; David A Campbell; Benedikt Vollrath; B S Shankaranarayana Rao; Hui-Yeon Ko; Gregory G Lin; Arvind Govindarajan; Se-Young Choi; Susumu Tonegawa
Journal:  Proc Natl Acad Sci U S A       Date:  2013-03-18       Impact factor: 11.205

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  17 in total

1.  Abnormal development of auditory responses in the inferior colliculus of a mouse model of Fragile X Syndrome.

Authors:  Anna O Nguyen; Devin K Binder; Iryna M Ethell; Khaleel A Razak
Journal:  J Neurophysiol       Date:  2020-04-22       Impact factor: 2.714

2.  A sound-driven cortical phase-locking change in the Fmr1 KO mouse requires Fmr1 deletion in a subpopulation of brainstem neurons.

Authors:  Andrew J Holley; Aleya Shedd; Anna Boggs; Jonathan Lovelace; Craig Erickson; Christina Gross; Miranda Jankovic; Khaleel Razak; Kimberly Huber; Jay R Gibson
Journal:  Neurobiol Dis       Date:  2022-05-17       Impact factor: 7.046

3.  Spontaneous seizures in adult Fmr1 knockout mice: FVB.129P2-Pde6b+Tyrc-chFmr1tm1Cgr/J.

Authors:  Jessica L Armstrong; Tanishka S Saraf; Omkar Bhatavdekar; Clinton E Canal
Journal:  Epilepsy Res       Date:  2022-03-08       Impact factor: 2.991

Review 4.  A review of decreased sound tolerance in autism: Definitions, phenomenology, and potential mechanisms.

Authors:  Zachary J Williams; Jason L He; Carissa J Cascio; Tiffany G Woynaroski
Journal:  Neurosci Biobehav Rev       Date:  2020-12-04       Impact factor: 8.989

5.  Dynamics of the fragile X mental retardation protein correlates with cellular and synaptic properties in primary auditory neurons following afferent deprivation.

Authors:  Xiaoyan Yu; Xiaoyu Wang; Hitomi Sakano; Diego A R Zorio; Yuan Wang
Journal:  J Comp Neurol       Date:  2020-06-27       Impact factor: 3.215

6.  Sex differences in resting EEG power in Fragile X Syndrome.

Authors:  Elizabeth G Smith; Ernest V Pedapati; Rui Liu; Lauren M Schmitt; Kelli C Dominick; Rebecca C Shaffer; John A Sweeney; Craig A Erickson
Journal:  J Psychiatr Res       Date:  2021-03-31       Impact factor: 5.250

7.  Temporal-specific roles of fragile X mental retardation protein in the development of the hindbrain auditory circuit.

Authors:  Xiaoyu Wang; Ayelet Kohl; Xiaoyan Yu; Diego A R Zorio; Avihu Klar; Dalit Sela-Donenfeld; Yuan Wang
Journal:  Development       Date:  2020-08-25       Impact factor: 6.862

8.  Deletion of BDNF in Pax2 Lineage-Derived Interneuron Precursors in the Hindbrain Hampers the Proportion of Excitation/Inhibition, Learning, and Behavior.

Authors:  Philipp Eckert; Philine Marchetta; Marie K Manthey; Michael H Walter; Sasa Jovanovic; Daria Savitska; Wibke Singer; Michele H Jacob; Lukas Rüttiger; Thomas Schimmang; Ivan Milenkovic; Peter K D Pilz; Marlies Knipper
Journal:  Front Mol Neurosci       Date:  2021-03-26       Impact factor: 5.639

9.  Altered brain-wide auditory networks in a zebrafish model of fragile X syndrome.

Authors:  Lena Constantin; Rebecca E Poulsen; Leandro A Scholz; Itia A Favre-Bulle; Michael A Taylor; Biao Sun; Geoffrey J Goodhill; Gilles C Vanwalleghem; Ethan K Scott
Journal:  BMC Biol       Date:  2020-09-16       Impact factor: 7.431

10.  Non-Apoptotic Caspase Activity Preferentially Targets a Novel Consensus Sequence Associated With Cytoskeletal Proteins in the Developing Auditory Brainstem.

Authors:  Forrest Weghorst; Yeva Mirzakhanyan; Kiersten L Hernandez; Paul D Gershon; Karina S Cramer
Journal:  Front Cell Dev Biol       Date:  2022-03-07
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