LII Electron Microscopy of the Inner Ear

1968 ◽  
Vol 77 (4) ◽  
pp. 629-643 ◽  
Author(s):  
Catherine A. Smith
1983 ◽  
Vol 92 (1_suppl) ◽  
pp. 3-12 ◽  
Author(s):  
Tomonori Takasaka ◽  
Hideich Shinkawa ◽  
Kozo Watanuki ◽  
Sho Hashimoto ◽  
Kazutomo Kawamoto

The technique and some preliminary results of the application of high-voltage electron microscopy (HVEM) to the study of inner ear morphology in the guinea pig are reported in this paper. The main advantage of HVEM is that sharp images of thicker specimens can be obtained because of the greater penetrating power of high energy electrons. The optimum thickness of the sections examined with an accelerating voltage of 1,000 kV was found to be between 500 to 800 nm. The sections below 500 nm in thickness often had insufficient contrast, while those above 800 nm were rather difficult to interpret due to overlap of images of the organelles. The whole structure of the sensory hairs from the tip to the rootlet was more frequently observed in the 800-nm thick sections. Thus the fine details of the hair attachment to the tectorial membrane as well as the hair rootlet extension into the cuticular plate could be thoroughly studied in the HVEM. In specimens fixed in aldehyde containing 2% tannic acid, the attachment of the tips of the outer hair cell stereocilia to the tectorial membrane was observed. For the inner hair cells, however, the tips of the hairs were separated from the undersurface of the tectorial membrane. The majority of the rootlets of the outer hair cells terminated at the midportion of the cuticular plate, while most of the inner hair cell rootlets traversed the entire width of the cuticular plate and extended into the apical cytoplasm. These differences in ultrastructural appearance may indicate that the two kinds of hair cells play different roles in the acoustic transduction process. The three-dimensional arrangement of the nerve endings on the hair cells was also studied by the serial thick-sectioning technique in the HVEM. In general, an entire arrangement of the nerve endings was almost completely cut in less than ten 800-nm thick sections instead of the 50- to 100-ultrathin (ie, less than 100 nm) conventional sections for transmission electron microscopy. The present study confirms an earlier report that the first row outer hair cells in the third cochlear turn are innervated by nearly equal numbers of efferent and afferent endings, the average number being nine.


Author(s):  
E. Ishiyama ◽  
J. Weibel ◽  
E. N. Myers

In recently years the distribution of the non-sensory specialized epithella in the inner ear has been interested among otologists. Increased understanding of the problem dealing with the fluid transport within the endolymph has been obtained these studied. To our knowledge, however, the distribution of the avian specialized cells in the inner ear has not been described adequately. In addition, ultrastructural characteristics of the osmiophilic(dark) cells in the avian labyrinth were not clearly demonstrated. Therefore, the specialized epithlia in the avian labyrinth should be further investigated and the nature of their function defined.To demonstrat this, pigeois were investigated using phase and electron-microscopy. The specialized cells(dark and light cells) were distributed in the crlstae ampullaris, the tegmentum vasculosum of the lagena which is analogous to the stria vascularis in mammals, the saccule, the otolith lagena, the utricle and the crista negletica.


2008 ◽  
Vol 139 (2_suppl) ◽  
pp. P195-P195
Author(s):  
Gao Xia

Problem The dendritic cell-derived BTB/POZ zinc finger (DPZF) protein belongs to the C2H2 zinc finger protein transcription factor family. It is localized on chromosome 3 and widely expressed in hematopoietic tissues, including human dendritic cells (DC), monocytes, B cells and T cells. DPZF null mice (DPZF-/-) exhibit a circling phenotype, suggestive of an inner ear defect. Here, we present our work on the role of DPZF in hearing defects. Methods We used auditory brainstem responses (ABR) and distortion production otoacoustic emissions (DPOAEs) to test the hearing function of DPZF-/- mice, then gross observation and histopathology analysis including serial sections and scanning electron microscopy were performed to exam the cochlea of DPZF-/- mice. Results Auditory brainstem responses (ABR) and distortion production otoacoustic emissions (DPOAEs) showed that DPZF-/-mice were completely deaf. Disorganized and fewer hair cells of the Corti organ in DPZF-/- mice were identified by scanning electron microscopy. Besides, although the hair cells of the utricle and saccule were grossly normal, the stereocilia were greatly reduced in number. Further more, lipofuscin was seen in the stria vascularis with the amount of which increased with age. Conclusion The impaired hearing and balance function and the morphological abnormalities of inner ears are caused by the deletion of DPZF gene. Significance DPZF gene may participates in regulating inner ear development and the DPZF null mice may serve as a new disease model of hearing loss. Support This work was supported by the ground of Jiangsu Province Famous Doctor Project(RC2007010).


1994 ◽  
Vol 4 (2) ◽  
pp. 43
Author(s):  
J. D. Cubillana ◽  
E. Benedito ◽  
L. M. Amorós ◽  
C. Ferrer ◽  
A. Zuasti ◽  
...  

1991 ◽  
Vol 545 (1-2) ◽  
pp. 223-233 ◽  
Author(s):  
Claude J. Dechesne ◽  
David R. Hampson ◽  
Gertrude Goping ◽  
Kathryn D. Wheaton ◽  
Robert J. Wenthold

Sign in / Sign up

Export Citation Format

Share Document