Skip to main content
Fig. 3 | BMC Genomics

Fig. 3

From: A murine model for the del(GJB6-D13S1830) deletion recapitulating the phenotype of human DFNB1 hearing impairment: generation and functional and histopathological study

Fig. 3

Cx30 expression in the cochlea of P30 Dfnb1em274 HOM mice. Representative micrographs of cochlear paraffin sections stained with hematoxylin–eosin (A, B) or immunostained against Cx30 (C, D), showing the basal region of WT (A, C) and Dfnb1em274 HOM (B, D) mice. WT mice present a normal cochlear cytoarchitecture and Cx30 expression in the spiral limbus, organ of Corti (surrounding supporting cells, arrows in C) and lateral wall. Dfnb1em274 HOM mice show a complete absence of Cx30 expression (D) and gross alterations in the Reissner membrane, tectorial membrane, and organ of Corti, compared to WT (B). LW, lateral wall; RM, Reissner membrane; SG, spiral ganglion; SL, spiral limbus; SM, scala media; ST, scala tympani; sTV, stria vascularis; SV, scala vestibuli. Scale bar: 100 mm

Back to article page