Suzumoto Reina, Takami Masamichi, Sasaki Takahisa
Department of Oral Histology, School of Dentistry, Showa University 1-5-8 Hatanodai, Tokyo 142-8555, Japan.
J Electron Microsc (Tokyo). 2005 Dec;54(6):529-40. doi: 10.1093/jmicro/dfi074. Epub 2006 Mar 1.
We examined the differentiation and resorptive function of osteoclasts (OC) cultured on the slices of calcified bone, decalcified bone and hyaline cartilage, and found that OC differentiation depends on the co-cultured substratum, as well as osteoblast-derived factors. Bone marrow-derived macrophages (BMM) were formed from marrow cells of 5 week old ddY mice and cultured for 3 days on freeze-dried slices of calcified bone, decalcified bone or cartilage, all prepared from rabbit costal bone. BMM cultured on calcified bone slices exhibited tartrate-resistant acid phosphatase (TRAP) activity and were structurally characterized by multinucleation and ruffled border development. However, on decalcified bone slices, BMM seldom became multinucleated and exhibited weak TRAP activity. BMM cultured on cartilage slices were mononuclear, devoid of TRAP activity and structurally resembled mononuclear phagocytes. In SEM observations of co-cultured slices, resorption lacunae were formed only on calcified bone slices, and not on slices of decalcified bone and cartilage. Our results, therefore, indicated that BMM could differentiate into functional OC only on calcified bone slices, suggesting a key role of calcified components in the bone matrix for the terminal OC differentiation. Then, we cultured BMM on the same slices with yeast particles. In cultures with yeast particles, BMM exhibited intense TRAP activity, developed a ruffled border-like structure and formed resorption lacunae even on decalcified bone and cartilage slices. Vacuolar-type H+-ATPase was strongly expressed along the ruffled border membranes of these OC. Only the BMM that had not incorporated yeast particles developed a ruffled border, whereas the BMM that had incorporated yeast particles did not become multinucleated and lacked a ruffled border structure. Thus, our results further suggest that, even on uncalcified substrata, the terminal differentiation of BMM into functional OC is induced by an unidentified external stimulus, which may be contained in the cell membrane of yeast particles.
我们研究了在钙化骨、脱钙骨和透明软骨切片上培养的破骨细胞(OC)的分化和吸收功能,发现OC的分化取决于共培养的基质以及成骨细胞衍生因子。骨髓来源的巨噬细胞(BMM)由5周龄ddY小鼠的骨髓细胞形成,并在均取自兔肋的钙化骨、脱钙骨或软骨的冻干切片上培养3天。在钙化骨切片上培养的BMM表现出抗酒石酸酸性磷酸酶(TRAP)活性,其结构特征为多核化和皱褶缘形成。然而,在脱钙骨切片上,BMM很少多核化,且TRAP活性较弱。在软骨切片上培养的BMM为单核,无TRAP活性,结构上类似于单核吞噬细胞。在共培养切片的扫描电镜观察中,仅在钙化骨切片上形成了吸收陷窝,而在脱钙骨和软骨切片上未形成。因此,我们的结果表明,BMM仅在钙化骨切片上可分化为功能性OC,提示骨基质中的钙化成分在OC终末分化中起关键作用。然后,我们将BMM与酵母颗粒在相同切片上培养。在有酵母颗粒的培养物中,BMM表现出强烈的TRAP活性,形成类似皱褶缘的结构,甚至在脱钙骨和软骨切片上也形成了吸收陷窝。液泡型H⁺-ATP酶沿这些OC的皱褶缘膜强烈表达。只有未摄取酵母颗粒的BMM形成了皱褶缘,而摄取了酵母颗粒的BMM未多核化且缺乏皱褶缘结构。因此,我们的结果进一步表明,即使在未钙化的基质上,BMM向功能性OC的终末分化也可由一种未知的外部刺激诱导,这种刺激可能存在于酵母颗粒的细胞膜中。