Smith P F, Gandolfi A J, Krumdieck C L, Putnam C W, Zukoski C F, Davis W M, Brendel K
Life Sci. 1985 Apr 8;36(14):1367-75. doi: 10.1016/0024-3205(85)90042-6.
The lack of a reproducible method for the production of thin tissue slices has hindered the use of liver slices as an in vitro tool for hepatotoxicity studies. Fresh human, rat, and rabbit liver was processed using a mechanical slicer. With this instrument, precision (5% of thickness) liver slices in the submillimeter range could be produced at a rapid rate. Slices were prepared from fresh livers in chilled, oxygenated buffer to minimize trauma. Following incubation for up to 20 h in a dynamic organ culture system, histology of incubated slices suggested that 250 m precision-cut slices were optimum in regard to morphology relative to liver slices incubated under conventional organ culture conditions. Addition of bromobenzene to the culture showed time-dependent hepatotoxicity based on two classic parameters of cell degeneration. Histological evidence is presented which suggests the usefulness of this system for hepatotoxicity studies and the production of focal necrosis in vitro.
缺乏一种可重复的薄组织切片制作方法,阻碍了肝切片作为体外肝毒性研究工具的应用。使用机械切片机对新鲜的人、大鼠和兔肝脏进行处理。利用该仪器,能够快速制作出亚毫米范围内精度为(厚度的5%)的肝脏切片。在冰冷的、充氧的缓冲液中从新鲜肝脏制备切片,以尽量减少损伤。在动态器官培养系统中孵育长达20小时后,孵育切片的组织学结果表明,就形态学而言,相对于在传统器官培养条件下孵育的肝脏切片,250微米精密切割的切片是最佳的。向培养物中添加溴苯,基于细胞变性的两个经典参数显示出时间依赖性肝毒性。本文提供的组织学证据表明该系统在肝毒性研究和体外局灶性坏死生成方面的有用性。