文献检索，用中文搜 PubMed

Suppr 超能文献

核心技术专利：CN118964589B侵权必究

核心技术专利：CN118964589B侵权必究

Hrabák A, Antoni F, Csuka I

1st Department of Biochemistry, Semmelweis University Medical School, Budapest, Hungary.

Int J Biochem. 1991;23(10):997-1003. doi: 10.1016/0020-711x(91)90136-b.

Murine macrophages showed a considerably higher in vitro arginase production in short time cultures than rat peritoneal cells. 2. The in vivo stimulation with casein or thioglycollate resulted in an enhanced in vitro enzyme production in mice. 3. The adherence is not the condition of the enzyme production. 4. The difference between the two species cannot be explained by the lack of bivalent ions, the absence of energy supply, proteolysis, the low number of macrophages or by the different cell types of the peritoneal exudate of mouse and rat. 5. The lysozyme production of murine and rat peritoneal macrophages was also investigated and no difference was observed between the two species.

与大鼠腹膜细胞相比，小鼠巨噬细胞在短时间培养中体外精氨酸酶产量显著更高。2. 用酪蛋白或巯基乙酸盐进行体内刺激可提高小鼠体外酶产量。3. 黏附并非酶产生的条件。4. 这两个物种之间的差异不能用二价离子缺乏、能量供应缺失、蛋白水解、巨噬细胞数量少或小鼠和大鼠腹膜渗出液的不同细胞类型来解释。5. 还研究了小鼠和大鼠腹膜巨噬细胞的溶菌酶产生情况，未观察到两个物种之间存在差异。

Hrabák A, Antoni F, Csuka I

1st Department of Biochemistry, Semmelweis University Medical School, Budapest, Hungary.

Int J Biochem. 1991;23(10):997-1003. doi: 10.1016/0020-711x(91)90136-b.

Murine macrophages showed a considerably higher in vitro arginase production in short time cultures than rat peritoneal cells. 2. The in vivo stimulation with casein or thioglycollate resulted in an enhanced in vitro enzyme production in mice. 3. The adherence is not the condition of the enzyme production. 4. The difference between the two species cannot be explained by the lack of bivalent ions, the absence of energy supply, proteolysis, the low number of macrophages or by the different cell types of the peritoneal exudate of mouse and rat. 5. The lysozyme production of murine and rat peritoneal macrophages was also investigated and no difference was observed between the two species.

与大鼠腹膜细胞相比，小鼠巨噬细胞在短时间培养中体外精氨酸酶产量显著更高。2. 用酪蛋白或巯基乙酸盐进行体内刺激可提高小鼠体外酶产量。3. 黏附并非酶产生的条件。4. 这两个物种之间的差异不能用二价离子缺乏、能量供应缺失、蛋白水解、巨噬细胞数量少或小鼠和大鼠腹膜渗出液的不同细胞类型来解释。5. 还研究了小鼠和大鼠腹膜巨噬细胞的溶菌酶产生情况，未观察到两个物种之间存在差异。