Hossain Kazi Sazzad, Amizuka Norio, Ikeda Nobuyki, Nozawa-Inoue Kayoko, Suzuki Akiko, Li Minqi, Takeuchi Kiichi, Aita Megumi, Kawano Yoshiro, Hoshino Masaaki, Oda Kimimitsu, Takagi Ritsuo, Maeda Takeyasu
Division of Oral and Maxillofacial Surgery, Department of Oral Health Science, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Microsc Res Tech. 2005 Aug 15;67(6):325-35. doi: 10.1002/jemt.20211.
The hypertrophic chondrocytes lack the ability to proliferate, thus permitting matrix mineralization as well as vascular invasion from the bone in both the mandibular condyle and the epiphyseal cartilage. This study attempted to verify whether the histological appearance of the hypertrophic chondrocytes is in a steady state during postnatal development of the mouse mandibular condyle. Type X collagen immunohistochemistry apparently distinguished the fibrous layer described previously as the "articular zone," "articular layer," and "resting zone" from the hypertrophic zone. Interestingly, the ratio of the type X collagen-positive hypertrophic zone in the entire condyle seemed higher in the early stages but decreased in the later stages. Some apparently compacted cells in the hypertrophic zone showed proliferating cell nuclear antigen (PCNA) immunoreaction, indicating the potential for cell proliferation at the early stages. As the mice matured, in contrast, they further enlarged and assumed typical features of hypertrophic chondrocytes. Apoptotic cells were also discernible in the hypertrophic zone at the early but not later stages. Consistent with morphological configurations of hypertrophic chondrocytes, immunoreactions for alkaline phosphatase, osteopontin, and type I collagen were prominent at the later stage, but not the early stage. Cartilaginous matrices demonstrated scattered patches of mineralization at the early stage, but increased in their volume and connectivity at the later stage. Thus, the spatial and temporal occurrence of these immunoreactions as well as apoptosis likely reflect the prematurity of hypertrophying cells at the early stage, and imply a physiological relevance during the early development of the mandibular condyles.
肥大软骨细胞缺乏增殖能力,从而使得下颌髁突和骨骺软骨中的基质矿化以及来自骨的血管侵入得以发生。本研究试图验证在小鼠下颌髁突出生后的发育过程中,肥大软骨细胞的组织学外观是否处于稳定状态。X型胶原免疫组化明显区分了先前被描述为“关节区”“关节层”和“静止区”的纤维层与肥大区。有趣的是,整个髁突中X型胶原阳性肥大区的比例在早期似乎较高,但在后期降低。肥大区一些明显致密的细胞显示增殖细胞核抗原(PCNA)免疫反应,表明在早期存在细胞增殖的潜力。相比之下,随着小鼠成熟,它们进一步增大并呈现出肥大软骨细胞的典型特征。在早期而非后期的肥大区也可辨别出凋亡细胞。与肥大软骨细胞的形态结构一致,碱性磷酸酶、骨桥蛋白和I型胶原的免疫反应在后期显著,但在早期不显著。软骨基质在早期显示出散在的矿化斑,但在后期其体积和连通性增加。因此,这些免疫反应以及凋亡的时空发生可能反映了早期肥大细胞的不成熟,并暗示在下颌髁突早期发育过程中的生理相关性。