人牙本质涎蛋白在COS-7细胞中的表达

目的 :构建人牙本质涎蛋白 (humandentinsialoprotein ,hDSP)真核表达载体 ,用瞬时系统表达目的基因。方法 :将hDSP全长基因定向克隆入真核表达质粒载体pcDNA3 ,构建pcDNA3 hDSP重组质粒 ,脂质体转染法转染COS 7细胞 ,48～ 72h收集细胞及培养上清 ,Westernblot和免疫组化检测表达产物。结果 :酶切鉴定表明重组表达载体构建成功 ;Westernblot检测显示在 60 0 0 0处出现一条清晰的特异性免疫阳性条带 ;免疫组化染色显示细胞胞质内有大量棕黄色颗粒 ,进一步证明该转染方法可行 ,转染效率较高。结论 :hDSP全长基因可以在COS 7细胞获得瞬时高效表达。

Transient expression of human dentin sialoprotein gene in COS-7 cells

Objective:To express human dentin sialoprotein (hDSP) gene in COS-7 cells. Methods:hDSP gene was subcloned into mammalian expression vector pcDNA3. The recombined plasmids were transfected into COS-7 cells using lipofectamune PLUS TM kit for transient expression. Western blot analysis and immunohistochemical staining were used to examine the gene products. Results:The constructed vectors were confirmed by digestion with restriction enzyme. An immuno-reaction positive band with relative molecular mass of 60 000 was found by Western blot analysis in culture supernatant and cytoplasms of COS-7 cells. Immunohistochemical staining showed strong positive particles in the cytoplasms. Conclution:hDSP gene can be expressed in COS-7 cells.