Expression of mRNA encoding extracellular matrix glycoproteins SPARC and SC1 is temporally and spatially regulated in the developing cochlea of the rat inner ear
- PMID: 11335086
- DOI: 10.1016/s0378-5955(01)00246-5
Expression of mRNA encoding extracellular matrix glycoproteins SPARC and SC1 is temporally and spatially regulated in the developing cochlea of the rat inner ear
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.
Similar articles
-
Differential mRNA expression of the related extracellular matrix glycoproteins SC1 and SPARC in the rat embryonic nervous system and skeletal structure.Brain Res. 2001 Feb 16;892(1):27-41. doi: 10.1016/s0006-8993(00)03141-3. Brain Res. 2001. PMID: 11172746
-
Cloning and expression of murine SC1, a gene product homologous to SPARC.J Histochem Cytochem. 1997 Jun;45(6):823-35. doi: 10.1177/002215549704500607. J Histochem Cytochem. 1997. PMID: 9199668
-
Induction of SC1 mRNA encoding a brain extracellular matrix glycoprotein related to SPARC following lesioning of the adult rat forebrain.Neurochem Res. 2000 Dec;25(12):1637-44. doi: 10.1023/a:1026626805612. Neurochem Res. 2000. PMID: 11152393
-
Hevin/SC1, a matricellular glycoprotein and potential tumor-suppressor of the SPARC/BM-40/Osteonectin family.Int J Biochem Cell Biol. 2004 Jun;36(6):991-6. doi: 10.1016/j.biocel.2004.01.017. Int J Biochem Cell Biol. 2004. PMID: 15094114 Review.
-
[Molecular biology of hearing].Laryngorhinootologie. 2011 Mar;90 Suppl 1:S22-34. doi: 10.1055/s-0030-1270444. Epub 2011 Apr 26. Laryngorhinootologie. 2011. PMID: 21523631 Review. German.
Cited by
-
Age-related changes in cochlear gene expression in normal and shaker 2 mice.J Assoc Res Otolaryngol. 2006 Sep;7(3):317-28. doi: 10.1007/s10162-006-0046-7. Epub 2006 Jun 23. J Assoc Res Otolaryngol. 2006. PMID: 16794912 Free PMC article.
-
Deafness and cochlear fibrocyte alterations in mice deficient for the inner ear protein otospiralin.Mol Cell Biol. 2005 Jan;25(2):847-53. doi: 10.1128/MCB.25.2.847-853.2005. Mol Cell Biol. 2005. PMID: 15632083 Free PMC article.
-
Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran.Clin Genet. 2021 Jul;100(1):59-78. doi: 10.1111/cge.13956. Epub 2021 Mar 24. Clin Genet. 2021. PMID: 33713422 Free PMC article.
-
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.J Hum Genet. 2003;48(11):564-70. doi: 10.1007/s10038-003-0079-2. Epub 2003 Oct 24. J Hum Genet. 2003. PMID: 14577002
-
Functional pathogenicity of ESRRB variant of uncertain significance contributes to hearing loss (DFNB35).Sci Rep. 2024 Sep 11;14(1):21215. doi: 10.1038/s41598-024-70795-8. Sci Rep. 2024. PMID: 39261511 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Miscellaneous