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   <subfield code="a">Transition of myosin heavy chain isoforms in human laryngeal abductors following denervation</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Xiaoxia Qiu, Donghui Chen, Meng Li, Yingna Gao, Fei Liu, Hongliang Zheng, Shicai Chen]</subfield>
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   <subfield code="a">The objective of this study was to investigate the myofiber subtype transition of human posterior cricoarytenoid (PCA) muscle after the injury to recurrent laryngeal nerve (RLN). PCA muscle specimens were obtained from 38 bilateral vocal fold paralysis patients underwent arytenoidectomy. According to the duration of RLN injury, all the cases were divided into five denervation groups: 6-12months, 1-2, 2-3, 3-6, and &gt;6years. The normal PCA muscles from total laryngectomy patients were chosen as controls. Immunofluorescence was adopted to detect the expression level of myosin heavy chain (MHC)-I and MHC-II in PCA muscle. Quantitative real-time PCR was also used to assess the transcriptional level of MHC subtypes (MHC-I, MHC-IIa, MHC-IIb, MHC-IIx, embryonic-MHC, and peri-natal-MHC). Immunofluorescence showed that MHC-I-positive myofibers in denervation groups were much lower than control group, respectively, while MHC-II-positive myofibers were significantly higher than control group (P&lt;0.05). With the extension of denervation, the number of MHC-I-positive myofibers gradually decreased, while MHC-II gradually increased and peaked in 1- to 2-year group. Transcriptional level of MHC-I, MHC-IIa, and MHC-IIb in denervation groups significantly down-regulated compared with the control (P&lt;0.05), respectively. However, MHC-IIx, embryonic-MHC, and peri-natal-MHC significantly up-regulated in all denervation groups, and the highest level was in 1- to 2-year denervation group. Data from the present study demonstrated that the maximum transition of MHC subtypes in human PCA muscles occurred in 1-2years after denervation, suggesting that laryngeal reinnervation before the occurrence of irreversible transition of MHC subtypes could maintain the structural integrity of laryngeal PCA muscles.</subfield>
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   <subfield code="a">Springer-Verlag Berlin Heidelberg, 2015</subfield>
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   <subfield code="a">Recurrent laryngeal nerve</subfield>
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   <subfield code="a">Vocal fold paralysis</subfield>
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   <subfield code="a">Myosin heavy chain</subfield>
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   <subfield code="a">Qiu</subfield>
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   <subfield code="u">Department of Otolaryngology-Head and Neck Surgery, Changhai Hospital, The Second Military Medical University, 200433, Shanghai, China</subfield>
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   <subfield code="a">Chen</subfield>
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   <subfield code="u">Department of Otolaryngology-Head and Neck Surgery, Changhai Hospital, The Second Military Medical University, 200433, Shanghai, China</subfield>
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   <subfield code="a">Li</subfield>
   <subfield code="D">Meng</subfield>
   <subfield code="u">Department of Otolaryngology-Head and Neck Surgery, Changhai Hospital, The Second Military Medical University, 200433, Shanghai, China</subfield>
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   <subfield code="a">Gao</subfield>
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   <subfield code="u">Department of Otolaryngology-Head and Neck Surgery, Changhai Hospital, The Second Military Medical University, 200433, Shanghai, China</subfield>
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   <subfield code="a">Liu</subfield>
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   <subfield code="u">Department of Otolaryngology-Head and Neck Surgery, Changhai Hospital, The Second Military Medical University, 200433, Shanghai, China</subfield>
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   <subfield code="u">Department of Otolaryngology-Head and Neck Surgery, Changhai Hospital, The Second Military Medical University, 200433, Shanghai, China</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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