Ossification process involving the human thoracic ligamentum flavum: role of transcription factors

被引:34
|
作者
Uchida, Kenzo [1 ]
Yayama, Takafumi [1 ]
Cai, Hong-Xin [1 ,2 ]
Nakajima, Hideaki [1 ]
Sugita, Daisuke [1 ]
Rodriguez Guerrero, Alexander [1 ,3 ]
Kobayashi, Shigeru [1 ]
Yoshida, Ai [1 ]
Chen, Ke-Bing [1 ,4 ]
Baba, Hisatoshi [1 ]
机构
[1] Univ Fukui, Dept Orthopaed & Rehabil Med, Fac Med Sci, Fukui 9101193, Japan
[2] Zhejiang Univ, Sir Run Run Shaw Hosp, Dept Orthoped Surg, Sch Med, Hangzhou 310016, Zhejiang, Peoples R China
[3] Univ El Salvador, Hosp Nacl Rosales, Serv Neurocirugia, San Salvador 1068000, El Salvador
[4] Sun Yat Sen Univ, Sch Med, Affiliated Hosp 1, Dept Spinal Surg, Guangzhou 510080, Guangdong, Peoples R China
关键词
POSTERIOR LONGITUDINAL LIGAMENT; CALCIUM CRYSTAL DEPOSITION; SPINAL-CANAL STENOSIS; CERVICAL-SPINE; LUMBAR SPINE; COMPRESSIVE MYELOPATHY; DECOMPRESSIVE SURGERY; MECHANICAL-STRESS; MIYAGI PREFECTURE; DIFFERENTIATION;
D O I
10.1186/ar3458
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Ossification of the ligamentum flavum (OLF) of the spine is associated with serious neurologic compromise, but the pathomechanism of this process remains unclear. The objective of this study was to investigate the pathomechanism of the ossification process, including the roles of various transcriptional factors in the ossification of human thoracic ligamentum flavum. Methods: Sections of the thoracic ligamentum flavum were obtained from 31 patients with OLF who underwent posterior thoracic decompression, and from six control patients free of OLF. Cultured ligamentum flavum cells (n = 6, each) were examined with real-time reverse transcription-polymerase chain reaction (RT-PCR) analysis for Sry-type high-mobility group box 9 (Sox9), runt-related transcription factor 2 (Runx2), muscle segment homeobox 2 (Msx2), Osterix, distal-less homeobox 5 (Dlx5), and AP-1. The harvested sections were examined with hematoxylin-eosin, the terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end-labeling (TUNEL) method, and immunohistochemistry for the transcriptional factors. Results: Compared with the control, the OLF showed disorganization of the elastic fiber bundles and abundant hypertrophic chondrocytes in the ossification front. TUNEL-positive chondrocytes were found near the ossified plaques. The mRNA expression levels of Sox9, Runx2, Msx2, and AP-1 in cultured cells from the ligamentum flavum of OLF patients were significantly different from those of the control. OLF samples were strongly immunoreactive to Sox9, Runx2, and Msx2 at proliferating chondrocytes in the fibrocartilage area. Hypertrophic chondrocytes were positive for Runx2, Osterix, Dlx5, and AP-1. Conclusions: The ossification process in OLF seems to involve chondrocyte differentiation under the unique expression of transcriptional factors. Accumulation of hypertrophic chondrocytes was evident around the calcified area at the ossification front, and we suggest that the differentiation of these cells seems to be concerned with the ossification process.
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页数:10
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