Scheven B A, Burger E H, Kawilarang-de Haas E W, Wassenaar A M, Nijweide P J
Lab Invest. 1985 Jul;53(1):72-9.
The effects of ionizing irradiation on the differentiation and activity of the osteoclast were investigated. Embryonic mouse metatarsal bones of different ages (14, 15, 16, 17 days) in which no osteoclasts had as yet been formed were irradiated with various x-ray doses and cultured until a marrow cavity became visible in the nonirradiated paired control bones. Bone growth and calcification were followed microscopically during culture. Irradiation caused a dose-dependent stunting of the longitudinal growth. Calcification was inhibited by high radiation doses (10 to 20 Gray (Gy), whereas a dose of 2.5 Gy stimulated the process in the early stages of long bone development. Histologic examination revealed complete inhibition of osteoclast formation in the 14- and 15-day-old bones after irradiation with 2.5 Gy or more. The number of osteoclasts in cultured older bones (16 days) was significantly reduced by irradiation, but osteoclast formation could not be completely prevented even by high dosages. Irradiation of explanted bone rudiments which were in a stage 1 day prior to the appearance of osteoclasts in vivo (17 days) did not significantly influence the formation of osteoclasts. Autoradiographic experiments using young bones showed that differentiation of osteoclast precursors into multinucleated osteoclasts is preceded by one or more divisions of the precursors in the periosteum. Furthermore, it was established from continuous 3H-thymidine-labeling experiments that in older bones (16 days) a part of the osteoclast nuclei originated from postmitotic osteoclast precursors. Irradiation mainly inhibited the appearance of labeled osteoclast nuclei in these bones. The results indicate that the osteoclast precursor, already present in the periosteum at an early stage of embryonic development, first proliferates and then differentiates into a mononuclear postmitotic preosteoclast. The proliferation is probably highly radiosensitive. Subsequently, the preosteoclasts fuse into multinucleated osteoclasts and invade the calcified hypertrophic cartilage zone. The resorbing activity of the osteoclast is less radiosensitive but can be inhibited by 5.0 Gy or more, as was established by morphometric and biochemical methods.
研究了电离辐射对破骨细胞分化和活性的影响。对不同年龄(14、15、16、17天)且尚未形成破骨细胞的胚胎小鼠跖骨进行不同剂量的X射线照射,并进行培养,直到未照射的配对对照骨中可见骨髓腔。在培养过程中通过显微镜观察骨生长和钙化情况。照射导致纵向生长出现剂量依赖性发育迟缓。高辐射剂量(10至20格雷(Gy))抑制钙化,而2.5 Gy的剂量在长骨发育早期刺激了这一过程。组织学检查显示,用2.5 Gy或更高剂量照射后,14天和15天大的骨骼中破骨细胞形成完全受到抑制。照射显著减少了培养的较老骨骼(16天)中破骨细胞的数量,但即使高剂量也不能完全阻止破骨细胞的形成。对体内破骨细胞出现前1天(17天)阶段的外植骨原基进行照射,对破骨细胞的形成没有显著影响。使用幼骨进行的放射自显影实验表明,破骨细胞前体分化为多核破骨细胞之前,前体在骨膜中会进行一次或多次分裂。此外,通过连续的3H-胸腺嘧啶核苷标记实验确定,在较老的骨骼(16天)中,一部分破骨细胞核起源于有丝分裂后的破骨细胞前体。照射主要抑制了这些骨骼中标记破骨细胞核的出现。结果表明,在胚胎发育早期已存在于骨膜中的破骨细胞前体,首先增殖,然后分化为单核有丝分裂后的前破骨细胞。增殖可能对辐射高度敏感。随后,前破骨细胞融合形成多核破骨细胞并侵入钙化的肥大软骨区。通过形态计量学和生化方法确定,破骨细胞的吸收活性对辐射的敏感性较低,但5.0 Gy或更高剂量可抑制其活性。