Albert Philippe, Boilly Bénoni
Laboratoire de Morphogenèse Animale, Universite des Sciences et Techniques de Lille-Flandres-Artois, F-59655, Villeneuve d'Ascq cedex, France.
Rouxs Arch Dev Biol. 1988 May;197(3):193-196. doi: 10.1007/BF00427924.
In order to study mitogenic control during axolotl limb regeneration, we have developed a primary blastema cell culture as a very sensitive bioassay for blastema mitogens. Transferrin, an iron-binding glycoprotein which has been shown to be the neurotrophic factor for muscle cells, is the mitogen which has been analysed in the present report. Addition of approximately 2 μg human transferrin/ ml of serum-free culture medium enhances blastema cell proliferation 11-fold over control levels and 2-fold over that produced by the addition of nerve extracts or purified growth factors extracted from nerve tissues (basic and acidic fetal growth factor, FGF). At a higher concentration (20 μg/ml), transferrin alone has no mitogenic effect unless the medium is also supplemented with FeCl (100 μM). The results are discussed with regard to the sensitivity of the blastema cell culture bioassay and in the context of the neurotrophic theory of urodele limb regeneration.
为了研究蝾螈肢体再生过程中的促有丝分裂控制,我们开发了一种原代芽基细胞培养方法,作为一种对芽基促有丝分裂原非常敏感的生物测定法。转铁蛋白是一种铁结合糖蛋白,已被证明是肌肉细胞的神经营养因子,是本报告中分析的促有丝分裂原。在无血清培养基中添加约2μg人转铁蛋白/ ml,可使芽基细胞增殖比对照水平提高11倍,比添加神经提取物或从神经组织中提取的纯化生长因子(碱性和酸性胎儿生长因子,FGF)所产生的增殖水平提高2倍。在较高浓度(20μg/ ml)下,单独的转铁蛋白没有促有丝分裂作用,除非培养基中还补充有FeCl(100μM)。我们将结合芽基细胞培养生物测定法的敏感性以及有尾两栖类肢体再生的神经营养理论来讨论这些结果。