Standardization of experimental animals temporal bone sections

Preparation of the temporal bone for light microscopy is an important step in histological studies of the inner ear. Due to the complexity of structures of the inner ear, it is difficult to measure or compare structures of interest without a commonly accepted standardized measure of temporal bone se...

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Published inJournal of otology Vol. 10; no. 2; pp. 66 - 71
Main Authors Ding, Dalian, Yu, Jintao, Li, Peng, Gao, Kelei, Jiang, Haiyan, Zhang, Wenjuan, Sun, Hong, Yin, Shankai, Salvi, Richard
Format Journal Article
LanguageEnglish
Published China Elsevier (Singapore) Pte Ltd 01.06.2015
Center for Hearing and Deafness, Department of Communicative Disorders and Sciences, University of New York at Buffalo, Buffalo, NY 14214, USA%Department of 0tolaryngology Head and Neck Surgery, Central South University Xiangya Hospital, Hunan, 410018, China%Department of 0tolaryngology Head and Neck Surgery, Union Hospital, Tongji Medical College of Huazhong University of Science&Technology, Wuhan, 430022, China%Department of 0tolaryngology Head and Neck Surgery, the Sixth People's Hospital of Shanghai Jiao Tong University, Shanghai, 200233, China
Chinese PLA General Hospital
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Summary:Preparation of the temporal bone for light microscopy is an important step in histological studies of the inner ear. Due to the complexity of structures of the inner ear, it is difficult to measure or compare structures of interest without a commonly accepted standardized measure of temporal bone sections. Therefore, standardization of temporal bone sections is very important for histological assessment of sensory hair cells and peripheral ganglion neurons in the cochlear and vestibular systems. The standardized temporal bone sectioning is oriented to a plane parallel to the outer and internal auditory canals. Sections are collected from the epitympanum to the hypotympanum to reveal layers in the order of the crista ampullaris of the superior and lateral semicircular canals, macula utriculi and macula sacculi, superior vestibular ganglion neurons, macula of saccule and inferior vestibular ganglion neurons, cochlear modiolus, endolymphatic duct and endolymphatic sac, and finally the crista ampullaris of the posterior semicircular canal. Moreover, technical details of preparing for temporal bone sectioning including fixation, decalcification, whole temporal bone staining, embedding penetration, and embedding orientation are also discussed.
Bibliography:Preparation of the temporal bone for light microscopy is an important step in histological studies of the inner ear. Due to the complexity of structures of the inner ear, it is difficult to measure or compare structures of interest without a commonly accepted standardized measure of temporal bone sections. Therefore, standardization of temporal bone sections is very important for histological assessment of sensory hair cells and peripheral ganglion neurons in the cochlear and vestibular systems. The standardized temporal bone sectioning is oriented to a plane parallel to the outer and internal auditory canals. Sections are collected from the epitympanum to the hypotympanum to reveal layers in the order of the crista ampullaris of the superior and lateral semicircular canals, macula utriculi and macula sacculi, superior vestibular ganglion neurons, macula of saccule and inferior vestibular ganglion neurons, cochlear modiolus, endolymphatic duct and endolymphatic sac, and finally the crista ampullaris of the posterior semicircular canal. Moreover, technical details of preparing for temporal bone sectioning including fixation, decalcification, whole temporal bone staining, embedding penetration, and embedding orientation are also discussed.
11-4883/R
Dalian Ding , Jintao Yu , Peng Li , Kelei Gao, Haiyan Jiang , Wenjuan Zhang, Hong Sun Shankai Yin, Richard Salvi (1.Department of Otolaryngology Head and Neck Surgery, Central South University Xiangya Hospital, Hunan, 410018, China;2.Center for Hearing and Deafness, Department of Communicative Disorders and Sciences, University of New York at Buffalo, Buffalo, NY 14214;3.Department of Otolaryngology Head and Neck Surgery, Sun Ya-sen University Third Hospital, Guangzhou, 510630, China;4.Department of Otolaryngology Head and Neck Surgery, Union Hospital, Tongji Medical College of Huazhong University of Science & Technology USA Wuhan,430022. China ;5.Department of Otolaryngology Head and Neck Surgery, the Sixth People's Hospital of Shanghai Jiao Tong University, Shanghai, 200233, China)
Experimental animal; Temporal bone section; Temporal bone; Collodion embedding; Decalcification
ISSN:1672-2930
2524-1753
DOI:10.1016/j.joto.2015.08.001