Nakamura T, Teramoto H, Tomita Y, Ichihara A
Biochem Biophys Res Commun. 1984 Aug 16;122(3):884-91. doi: 10.1016/0006-291x(84)91173-2.
For improvement of the culture conditions of adult rat hepatocytes in primary culture in collagen coated dishes, effects of various commercial culture media on the induction of replicative DNA synthesis of the cells stimulated by insulin plus epidermal growth factor were studied. Proline-deficient media, such as Leibovitz's L-15, Eagle's minimal essential medium and Dulbecco's modified minimal essential medium, did not induce DNA synthesis in hepatocytes, whereas proline-rich media, such as Williams medium E, McCoy's 5A and Ham's F-12, induced markedly hepatocyte proliferation. Moreover, when the proline-deficient media were supplemented with L-proline, the cells synthesized DNA in response to the two hormones. Cis-4-hydroxyl-L-proline strongly inhibited the induction of DNA synthesis, without affecting protein synthesis of the cells or showing any cytotoxicity. This inhibition was recovered completely by adding excess proline to the medium. Addition of other amino acids not present in the medium did not promote DNA synthesis. These findings indicate that L-proline is essential for induction of hepatocyte proliferation in culture, through its affect on synthesis of intracellular collagen.
为改善成年大鼠原代培养肝细胞在胶原包被培养皿中的培养条件,研究了各种商业培养基对胰岛素加表皮生长因子刺激的细胞复制性DNA合成诱导的影响。缺乏脯氨酸的培养基,如莱博维茨L-15培养基、伊格尔最低必需培养基和杜尔贝科改良最低必需培养基,不能诱导肝细胞中的DNA合成,而富含脯氨酸的培养基,如威廉姆斯E培养基、麦科伊5A培养基和哈姆F-12培养基,则能显著诱导肝细胞增殖。此外,当向缺乏脯氨酸的培养基中添加L-脯氨酸时,细胞会对这两种激素作出反应合成DNA。顺式-4-羟基-L-脯氨酸强烈抑制DNA合成的诱导,而不影响细胞的蛋白质合成,也未显示出任何细胞毒性。通过向培养基中添加过量脯氨酸,这种抑制作用可完全恢复。添加培养基中不存在的其他氨基酸并不能促进DNA合成。这些发现表明,L-脯氨酸通过影响细胞内胶原蛋白的合成,对培养中肝细胞增殖的诱导至关重要。