Literature DB >> 11335086

Expression of mRNA encoding extracellular matrix glycoproteins SPARC and SC1 is temporally and spatially regulated in the developing cochlea of the rat inner ear.

A J Mothe1, I R Brown.   

Abstract

SPARC is a multifunctional extracellular matrix (ECM) glycoprotein that shares partial sequence homology with SC1/hevin. These ECM molecules exhibit calcium-binding properties and modulate cellular interactions. This study examines the expression of SC1 and SPARC mRNA in the developing cochlea of the rat inner ear prior to and after the onset of hearing. At all ages examined, SC1 mRNA is highly expressed in neurons of the spiral ganglion. In contrast, SPARC transcripts are not detected in the spiral ganglion but are enriched in the temporal bone and cartilaginous otic capsule surrounding the cochlea. Both SC1 and SPARC mRNA are expressed in connective tissue elements involved in maintaining ionic homeostasis of cochlear fluids. SC1 mRNA is localized to type III fibrocytes of the spiral ligament (slg) and marginal cells of the stria vascularis, while SPARC mRNA is apparent in the spiral limbus and type I fibrocytes of the slg. At postnatal day 10, SPARC mRNA shows a dramatic change in expression. High levels of SPARC transcripts are induced in Deiters cells (dc) of the organ of Corti. Interestingly, this induction of SPARC mRNA correlates with the onset of hearing. This suggests that SPARC may play a role in calcium regulation in dc when functional maturation of the cochlea is attained and rapid changes in calcium levels are required.

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Year:  2001        PMID: 11335086     DOI: 10.1016/s0378-5955(01)00246-5

Source DB:  PubMed          Journal:  Hear Res        ISSN: 0378-5955            Impact factor:   3.208


  9 in total

1.  Matricellular homologs in the foreign body response: hevin suppresses inflammation, but hevin and SPARC together diminish angiogenesis.

Authors:  Thomas H Barker; Paul Framson; Pauli A Puolakkainen; May Reed; Sarah E Funk; E Helene Sage
Journal:  Am J Pathol       Date:  2005-03       Impact factor: 4.307

2.  Age-related changes in cochlear gene expression in normal and shaker 2 mice.

Authors:  Tzy-Wen L Gong; I Jill Karolyi; James Macdonald; Lisa Beyer; Yehoash Raphael; David C Kohrman; Sally A Camper; Margaret I Lomax
Journal:  J Assoc Res Otolaryngol       Date:  2006-06-23

3.  Downregulation of otospiralin, a novel inner ear protein, causes hair cell degeneration and deafness.

Authors:  Benjamin Delprat; Ana Boulanger; Jing Wang; Vicky Beaudoin; Matthieu J Guitton; Stephanie Ventéo; Claude J Dechesne; Rémy Pujol; Mireille Lavigne-Rebillard; Jean-Luc Puel; Christian P Hamel
Journal:  J Neurosci       Date:  2002-03-01       Impact factor: 6.167

4.  Deafness and cochlear fibrocyte alterations in mice deficient for the inner ear protein otospiralin.

Authors:  Benjamin Delprat; Jérôme Ruel; Matthieu J Guitton; Ghyslaine Hamard; Marc Lenoir; Rémy Pujol; Jean-Luc Puel; Philippe Brabet; Christian P Hamel
Journal:  Mol Cell Biol       Date:  2005-01       Impact factor: 4.272

5.  Expression, functional, and structural analysis of proteins critical for otoconia development.

Authors:  Yinfang Xu; Hui Zhang; Hua Yang; Xing Zhao; Sándor Lovas; Yunxia Yesha Wang Lundberg
Journal:  Dev Dyn       Date:  2010-10       Impact factor: 3.780

6.  Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing loss.

Authors:  Satoko Abe; Shin-ichi Usami; Yusuke Nakamura
Journal:  J Hum Genet       Date:  2003-10-24       Impact factor: 3.172

7.  Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran.

Authors:  Marzieh Mohseni; Mojgan Babanejad; Kevin T Booth; Payman Jamali; Khadijeh Jalalvand; Behzad Davarnia; Fariba Ardalani; Atefeh Khoshaeen; Sanaz Arzhangi; Fatemeh Ghodratpour; Maryam Beheshtian; Faezeh Jahanshad; Hasan Otukesh; Fatemeh Bahrami; Seyed Morteza Seifati; Niloofar Bazazzadegan; Farkhonde Habibi; Hanieh Behravan; Sepide Mirzaei; Fatemeh Keshavarzi; Nooshin Nikzat; Zohreh Mehrjoo; Holger Thiele; Michael Nothnagel; Hela Azaiez; Richard J Smith; Kimia Kahrizi; Hossein Najmabadi
Journal:  Clin Genet       Date:  2021-03-24       Impact factor: 4.438

8.  A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing.

Authors:  Giulia Soldà; Michela Robusto; Paola Primignani; Pierangela Castorina; Elena Benzoni; Antonio Cesarani; Umberto Ambrosetti; Rosanna Asselta; Stefano Duga
Journal:  Hum Mol Genet       Date:  2011-10-28       Impact factor: 6.150

9.  Expression and function of scleraxis in the developing auditory system.

Authors:  Zoe F Mann; Weise Chang; Kyu Yup Lee; Kelly A King; Matthew W Kelley
Journal:  PLoS One       Date:  2013-09-13       Impact factor: 3.240

  9 in total

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