Watanabe J, Amizuka N, Noda T, Ozawa H
Department of Pedodontics, Faculty of Dentistry, Niigata University, Japan.
Cell Tissue Res. 2000 Sep;301(3):375-87. doi: 10.1007/s004410000242.
Since odontoclasts share similar characteristics with osteoclasts, this study has examined whether odontoclasts exhibit cytological alteration after treatment with bisphosphonate, which induces apoptosis of osteoclasts. After the administration of bisphosphonate to 6-day-old rabbits, many odontoclasts detached from the dentine surface of the deciduous teeth, resulting in the reduction of tartrate-resistant acid phosphatase (TRAP-ase) and immunoreactivity for cathepsin K. Transmission electron microscopy revealed a number of odontoclasts showing poorly developed or a lack of ruffled borders, a Golgi apparatus markedly reduced in size, and numerous cytoplasmic vesicles. The bisphosphonate-treated odontoclasts displayed fragmented DNA in the pyknotic nuclei evidenced by terminal deoxynucleotidyl-transferase-mediated dUTP-biotin nick-end labeling, indicating that bisphosphonate can induce apoptosis of the odontoclasts. Ultrastructural observations of the apoptotic odontoclasts revealed condensed heterochromatin at the margin of the nuclear envelope, assembled arrays of rough endoplasmic reticulum, and many vacuoles and vesicles. Some apoptotic odontoclasts showed ladder-like structures between the adjacent nuclear envelopes, enlargement of the nuclear envelopes, and the formation of a ribosome-like granular structure in the nuclei. Thus, odontoclasts are able to undergo apoptosis after bisphosphonate treatment; this results in cytological alterations, including reduced resorption activity and the inhibition of protein synthesis/transport as indicated by the diminished TRAPase and cathepsin K and the poorly developed Golgi apparatus, respectively. Nuclear alteration as evidenced by the appearance of ladder-like and ribosome-like structures was characteristic of apoptotic odontoclasts.
由于破牙细胞与破骨细胞具有相似的特征,本研究检测了破牙细胞在用双膦酸盐治疗后是否表现出细胞学改变,双膦酸盐可诱导破骨细胞凋亡。给6日龄家兔施用双膦酸盐后,许多破牙细胞从乳牙的牙本质表面脱离,导致抗酒石酸酸性磷酸酶(TRAP酶)减少以及组织蛋白酶K的免疫反应性降低。透射电子显微镜显示,许多破牙细胞的皱褶缘发育不良或缺失,高尔基体大小明显减小,并且有大量细胞质小泡。经双膦酸盐处理的破牙细胞在固缩核中显示出DNA片段化,这通过末端脱氧核苷酸转移酶介导的dUTP生物素缺口末端标记得以证实,表明双膦酸盐可诱导破牙细胞凋亡。对凋亡破牙细胞的超微结构观察显示,核膜边缘有浓缩的异染色质、粗面内质网排列成阵列,以及许多液泡和小泡。一些凋亡破牙细胞在相邻核膜之间显示出梯状结构、核膜扩大以及核内形成核糖体样颗粒结构。因此,破牙细胞在双膦酸盐处理后能够发生凋亡;这导致细胞学改变,包括吸收活性降低以及蛋白质合成/运输受到抑制,分别表现为TRAP酶和组织蛋白酶K减少以及高尔基体发育不良。梯状和核糖体样结构的出现所证明的核改变是凋亡破牙细胞的特征。