TY - JOUR
T1 - Fine morphology of bony dysplasia of the murine ear
T2 - Comparisons with otosclerosis
AU - Chole, Richard A.
AU - Tinling, Steven P.
N1 - Funding Information:
Received from the Departmeut of Otolarytlgology-Head and Neck Surgery, University of California a{ \[)avis, Davis, California. Presented at the Workshop oll Recent Advances in Otosclerosis Research, Tenth Midwinter Research Meeting, Association for Research in Otolaryngo\]ogy, February 4, 1987, Clearwater Beach, Florida. Accepted for publication at that time. Accepted for publication at that time. Supported by NIH grant NS 21573. Address reprint requests to Dr. Chole: Otology Laboratory, 1159 Surge \[\[IU, niversity of California at Davis, Davis, CA 95616. 0196-0709/87 $0.00 + .25
PY - 1987
Y1 - 1987
N2 - Dysplastic bony lesions that bear certain similarities to otosclerosis occur spontaneously in LP/J inbred mice. These lesions develop after the fifth week of life and progressively enlarge; they are present in 90% of animals by 90 weeks of age. In the present study, the fine morphology of these lesions was investigated. Dysplastic lesions in the middle ear of LP/J mice appeared to begin as subperiosteal accumulations of amorphous material. These accumulations occurred adjacent to the bone surface below the epithelium of the middle ear. This amorphous material was often associated with macrophages on the adjacent epithelial surface. The material appeared to be replaced with collagen fibers in a disorganized manner, forming a homogeneous base (osteoid) on which calcification occurred. The fine morphology and periodicity of the collagen appeared normal. The lesions then calcified by forming calcospherites that became confluent. During this period, transformed fibroblasts (osteoblasts) appeared in the calcifying matrix, resulting in a lesion made of bone. These lesions could sometimes be seen replacing normal bony contours but most often were exophytic. The lesions at all stages of development may be associated with macrophages and effusions in the middle ear. The lesions in the middle ear of LP/J mice appeared to develop by an active process of bone formation; in contrast, otosclerosis is an active process of bone resorption and formation.
AB - Dysplastic bony lesions that bear certain similarities to otosclerosis occur spontaneously in LP/J inbred mice. These lesions develop after the fifth week of life and progressively enlarge; they are present in 90% of animals by 90 weeks of age. In the present study, the fine morphology of these lesions was investigated. Dysplastic lesions in the middle ear of LP/J mice appeared to begin as subperiosteal accumulations of amorphous material. These accumulations occurred adjacent to the bone surface below the epithelium of the middle ear. This amorphous material was often associated with macrophages on the adjacent epithelial surface. The material appeared to be replaced with collagen fibers in a disorganized manner, forming a homogeneous base (osteoid) on which calcification occurred. The fine morphology and periodicity of the collagen appeared normal. The lesions then calcified by forming calcospherites that became confluent. During this period, transformed fibroblasts (osteoblasts) appeared in the calcifying matrix, resulting in a lesion made of bone. These lesions could sometimes be seen replacing normal bony contours but most often were exophytic. The lesions at all stages of development may be associated with macrophages and effusions in the middle ear. The lesions in the middle ear of LP/J mice appeared to develop by an active process of bone formation; in contrast, otosclerosis is an active process of bone resorption and formation.
UR - http://www.scopus.com/inward/record.url?scp=0023624411&partnerID=8YFLogxK
U2 - 10.1016/S0196-0709(87)80051-0
DO - 10.1016/S0196-0709(87)80051-0
M3 - Article
C2 - 3434669
AN - SCOPUS:0023624411
SN - 0196-0709
VL - 8
SP - 325
EP - 331
JO - American Journal of Otolaryngology - Head and Neck Medicine and Surgery
JF - American Journal of Otolaryngology - Head and Neck Medicine and Surgery
IS - 5
ER -