Rouleau M F, Mitchell J, Goltzman D
Department of Medicine, McGill University, Montreal, Quebec, Canada.
Endocrinology. 1988 Jul;123(1):187-91. doi: 10.1210/endo-123-1-187.
Previous studies in vitro and in vivo have demonstrated the presence of receptor sites for PTH on cells of the osteoblast phenotype. Nevertheless, it is unclear whether the diverse functions of this hormone in bone can all be attributed to its interaction with a single cell type. In this study, we have used a radioautographic method to examine the competitive binding of 125I-labeled rat PTH-(1-34) to the long bones of rats in vivo. Our studies confirm the presence of competitive binding to mature osteoblasts and the absence of significant competitive binding to multinucleated osteoclasts. However, by light and electron microscopic radioautographic analysis, the majority of specific competitive PTH binding was present over a cell in the intertrabecular space of the metaphyseal region, which was distinct from the mature osteoblast. This large mononuclear cell with multiple cytoplasmic extensions appeared to interface with both the bone matrix and the microvascular osseous circulation and may provide an additional target to mediate hormonal effects on the skeleton.
先前的体外和体内研究已证明成骨细胞表型的细胞上存在甲状旁腺激素(PTH)的受体位点。然而,尚不清楚该激素在骨骼中的多种功能是否都可归因于其与单一细胞类型的相互作用。在本研究中,我们使用放射自显影方法来检测体内125I标记的大鼠PTH-(1-34)与大鼠长骨的竞争性结合。我们的研究证实了与成熟成骨细胞存在竞争性结合,而与多核破骨细胞不存在明显的竞争性结合。然而,通过光镜和电镜放射自显影分析,大部分特异性竞争性PTH结合出现在干骺端区域小梁间隙中的一种细胞上,该细胞不同于成熟成骨细胞。这种具有多个细胞质突起的大单核细胞似乎与骨基质和微血管骨循环都有界面接触,并且可能为介导激素对骨骼的作用提供额外的靶点。