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Thrombospondins 1 and 2 are important for afferent synapse formation and function in the inner ear

  • Diana Mendus
  • , Srividya Sundaresan
  • , Nicolas Grillet
  • , Felix Wangsawihardja
  • , Rose Leu
  • , Ulrich Müller
  • , Sherri M. Jones
  • , Mirna Mustapha

Producción científica: Articlerevisión exhaustiva

24 Citas (Scopus)

Resumen

Thrombospondins (TSPs) constitute a family of secreted extracellular matrix proteins that have been shown to be involved in the formation of synapses in the central nervous system. In this study, we show that TSP1 and TSP2 are expressed in the cochlea, and offer the first description of their putative roles in afferent synapse development and function in the inner ear. We examined mice with deletions of TSP1, TSP2 and both (TSP1/TSP2) for inner ear development and function. Immunostaining for synaptic markers indicated a significant decrease in the number of formed afferent synapses in the cochleae of TSP2 and TSP1/TSP2 knockout (KO) mice at postnatal day (P)29. In functional studies, TSP2 and TSP1/TSP2 KO mice showed elevated auditory brainstem response (ABR) thresholds as compared with wild-type littermates, starting at P15, with the most severe phenotype being seen for TSP1/TSP2 KO mice. TSP1/TSP2 KO mice also showed reduced wave I amplitudes of ABRs and vestibular evoked potentials, suggesting synaptic dysfunction in both the auditory and vestibular systems. Whereas ABR thresholds in TSP1 KO mice were relatively unaffected at early ages, TSP1/TSP2 KO mice showed the most severe phenotype among all of the genotypes tested, suggesting functional redundancy between the two genes. On the basis of the above results, we propose that TSPs play an important role in afferent synapse development and function of the inner ear.

Idioma originalEnglish
Páginas (desde-hasta)1256-1267
Número de páginas12
PublicaciónEuropean Journal of Neuroscience
Volumen39
N.º8
DOI
EstadoPublished - abr 2014

Financiación

FinanciadoresNúmero del financiador
National Institute on Deafness and Other Communication DisordersR01 DC006443, P30 DC010363, RO1 DC09590, R01DC006443

    ASJC Scopus subject areas

    • General Neuroscience

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