Interdisciplinary Research Center in Biomedical Materials, COMSATS Institute of Information Technology, Defence Road, Off Raiwind Road, Lahore, Pakistan ; Institue of Biology, Leiden University, Sylvius Laboratory, Leiden, The Netherlands.
Institue of Biology, Leiden University, Sylvius Laboratory, Leiden, The Netherlands.
Cell J. 2014 Summer;16(2):211-24. Epub 2014 May 25.
Genes involved in bone and tissue remodelling in the vertebrates include matrix metalloproteinase-9 (mmp-9), receptor activator of necrosis factor κ-β (rank), cathepsin-k (Ctsk) and tartrate-resistant acid phosphatase (TRAcP). We examine whether these markers are expressed in cells of zebrafish embryos of 1-5 days post fertilization. We also examine adult scales, which are known to contain mature osteoclasts, for comparison.
In this experimental study, in situ hybrdisation, histochemistry and serial plastic and paraffin sectioning were used to analyse marker expression.
We found that mmp-9 mRNA, TRAcP enzyme and Ctsk YFP protein were expressed in haematopoietic tissues and in the cells scattered sparsely in the embryo. Ctsk and rank mRNA were both expressed in the branchial skeleton and in the developing pectoral fin. In these skeletal structures, histology showed that the expressing cells were located around the developing cartilage elements, in the parachondral tissue. In a transgenic zebrafish line with YFP coupled to Ctsk promoter, Ctsk expressing cells were found around pharyngeal skeletal elements. To see whether we could activate osteoclasts, we exposed prim-6 zebrafish embryos to a mixture of 1 µM dexamethasone and 1 µM vitaminutes D3. These compounds, which are known to trigger osteoclastogenensis in cell cultures, lead to an increase in intensity of Ctsk YFP expression around the skeletal elements.
Our findings show that cells expressing a range of osteoclast markers are present in early larvae and can be activated by the addition of osteoclastogenic compounds.
脊椎动物中参与骨和组织重塑的基因包括基质金属蛋白酶-9(mmp-9)、核因子 κ-β 受体激活剂(rank)、组织蛋白酶 K(Ctsk)和抗酒石酸酸性磷酸酶(TRAcP)。我们检查这些标记物是否在受精后 1-5 天的斑马鱼胚胎细胞中表达。我们还检查了已知含有成熟破骨细胞的成年鳞片,作为比较。
在这项实验研究中,我们使用原位杂交、组织化学和连续塑料和石蜡切片来分析标记物的表达。
我们发现 mmp-9 mRNA、TRAcP 酶和 Ctsk YFP 蛋白在造血组织和胚胎中稀疏分布的细胞中表达。Ctsk 和 rank mRNA 均在鳃骨和正在发育的胸鳍中表达。在这些骨骼结构中,组织学显示表达细胞位于正在发育的软骨元素周围,位于软骨旁组织中。在带有 Ctsk 启动子与 YFP 偶联的转基因斑马鱼系中,发现 Ctsk 表达细胞位于咽骨元素周围。为了观察我们是否可以激活破骨细胞,我们将 prim-6 斑马鱼胚胎暴露于 1µM 地塞米松和 1µM 维生素 D3 的混合物中。这些化合物已知在细胞培养中触发破骨细胞生成,导致骨骼元素周围 Ctsk YFP 表达强度增加。
我们的发现表明,表达一系列破骨细胞标记物的细胞存在于早期幼虫中,可以通过添加破骨细胞生成化合物来激活。