Sawae Yoshiko, Sahara Takako, Sasaki Takahisa
Department of Oral Histology, School of Dentistry, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan.
J Electron Microsc (Tokyo). 2003;52(6):493-502. doi: 10.1093/jmicro/52.6.493.
Using 3-day-old newborn rats, we examined the differentiation processes of osteoclasts associated with the destruction of the femoral growth plate cartilage and primary trabecular bone. In the growth plate cartilage, thin mineralized areas were detected solely in the longitudinal septal cartilage matrix in the hypertrophic zone, but the transverse septal cartilage matrix between adjacent chondrocytic lacunae within a row of chondrocytes remained unmineralized. The longitudinal septal cartilage between adjacent rows of chondrocytes appeared to persist, forming the walls of opened lacunar canals. Consistent with the removal of the transverse septal cartilage matrix, the longitudinal canals of opened chondrocytic lacunae were deeply invaded by capillary vessels, mononuclear cells and multinucleated pre-osteoclasts lacking a ruffled border. CD34-positive endothelial cells of capillary vessels deeply penetrated into the transverse septal cartilage matrix facing the medullary cavity and the opened chondrocytic lacunae. ED1-positive monocytes/macrophages were distributed at the chondro-osseous junction, but they were distant from the erosive front of the transverse septa. Tartrate-resistant acid phosphatase-positive multinucleated pre-osteoclasts lacking a ruffled border and differentiated osteoclasts with a ruffled border were localized mainly at two locations: the chondro-osseous junction and the growth front of primary bone trabeculae. Osteoclasts were located on the type-I collagen-positive bone trabeculae close to the growth plate, but they appeared to be distant from the type-II collagen-positive cartilage matrix. Even within opened chondrocytic lacunae, when osteoclasts were distant from the cartilage and bone matrix, they lacked polarized cytoplasmic organization and a ruffled border. The osteoclasts located in the remaining septal cartilage also exhibited neither a ruffled border nor a clear zone. Osteoclasts with a prominent ruffled border and clear zone were located in bone matrix covering the remaining septal cartilage. These results suggest that osteoclasts require hydroxyapatite crystals and bone matrix constituents for ruffled border formation and are not involved in resorption of the unmineralized transverse and mineralized longitudinal septal cartilage without covering bone matrix at the chondro-osseous junction.
利用3日龄新生大鼠,我们研究了与股骨生长板软骨和初级小梁骨破坏相关的破骨细胞分化过程。在生长板软骨中,仅在肥大区的纵向间隔软骨基质中检测到薄的矿化区域,但一排软骨细胞内相邻软骨细胞腔隙之间的横向间隔软骨基质仍未矿化。相邻排软骨细胞之间的纵向间隔软骨似乎持续存在,形成开放的腔隙管的壁。与横向间隔软骨基质的去除一致,开放的软骨细胞腔隙的纵向管被毛细血管、单核细胞和缺乏皱褶边缘的多核前破骨细胞深深侵入。毛细血管的CD34阳性内皮细胞深深穿透面向骨髓腔和开放的软骨细胞腔隙的横向间隔软骨基质。ED1阳性单核细胞/巨噬细胞分布在软骨-骨交界处,但它们远离横向间隔的侵蚀前沿。缺乏皱褶边缘的抗酒石酸酸性磷酸酶阳性多核前破骨细胞和具有皱褶边缘的分化破骨细胞主要定位于两个位置:软骨-骨交界处和初级骨小梁的生长前沿。破骨细胞位于靠近生长板的I型胶原阳性骨小梁上,但它们似乎远离II型胶原阳性软骨基质。即使在开放的软骨细胞腔隙内,当破骨细胞远离软骨和骨基质时,它们也缺乏极化的细胞质组织和皱褶边缘。位于剩余间隔软骨中的破骨细胞也既没有皱褶边缘也没有清晰区。具有突出皱褶边缘和清晰区的破骨细胞位于覆盖剩余间隔软骨的骨基质中。这些结果表明,破骨细胞形成皱褶边缘需要羟基磷灰石晶体和骨基质成分,并且在软骨-骨交界处不参与未矿化的横向和矿化的纵向间隔软骨的吸收,除非有覆盖的骨基质。