Gouin F, Couillaud S, Cottrel M, Godard A, Passuti N, Heymann D
Faculté de Chirurgie Dentaire, Centre de Recherche Interdisciplinaire sur les Tissus Calcifiés et les Biomatériaux, UPRES EA 2159, 1 Pl. Alexis Ricordeau, Nantes Cedex 01, 44042, France.
Cytokine. 1999 Apr;11(4):282-9. doi: 10.1006/cyto.1998.0429.
The behaviour of multinucleated giant cells (MNC) obtained from a giant cell tumour of the tibia and cultured on glass coverslips or on devitalized dentin slices was investigated using light and electron microscopy. Cells were studied in the presence or absence of LIF a cytokine known to be involved in bone turnover and to act as a growth factor in some solid tumours. The direct effect of LIF on MNC was examined by a post-embedding colloidal gold immunocytochemistry process using human anti-LIF and anti-LIF-receptor (chain gp190) antibodies. After 7 days of culture, the MNC obtained displayed osteoclast immunocytochemical features. Moreover, these MNC were able to resorb large amounts of dentin and presented typical features of active osteoclasts. Immunolocalization of LIF and LIF-receptor revealed the presence of this cytokine and its receptor within the cytoplasm and nucleus of active resorbing MNC. LIF upmodulated MNC number and nucleation but decreased their ability to resorb dentin. The present study suggests that MNC obtained from human GCT, currently considered as osteoclast-like cells, are targets for LIF and may be a source of LIF production in this pathological condition.
利用光学显微镜和电子显微镜,对取自胫骨巨细胞瘤并在玻璃盖玻片或失活牙本质切片上培养的多核巨细胞(MNC)的行为进行了研究。在有或没有白血病抑制因子(LIF)的情况下对细胞进行研究,LIF是一种已知参与骨转换并在某些实体瘤中充当生长因子的细胞因子。使用人抗LIF和抗LIF受体(链gp190)抗体,通过包埋后胶体金免疫细胞化学方法检测LIF对MNC的直接作用。培养7天后,获得的MNC表现出破骨细胞免疫细胞化学特征。此外,这些MNC能够吸收大量牙本质,并呈现出活跃破骨细胞的典型特征。LIF和LIF受体的免疫定位显示,在活跃吸收的MNC的细胞质和细胞核内存在这种细胞因子及其受体。LIF上调了MNC的数量和成核,但降低了它们吸收牙本质的能力。本研究表明,从人类巨细胞瘤获得的MNC,目前被认为是破骨细胞样细胞,是LIF的靶标,并且在这种病理状态下可能是LIF产生的来源。