La Rocca P J, Rheinwald J G
In Vitro Cell Dev Biol. 1985 Jan;21(1):67-72. doi: 10.1007/BF02620917.
This laboratory recently reported that normal human mesothelial cells require epidermal growth factor (EGF) and hydrocortisone (HC), in addition to fetal calf serum and a complex defined medium component, in order to grow optimally in surface culture. We report here that this normal cell type also forms large colonies at high efficiency in semi-solid medium, but exhibits more stringent serum and EGF requirements for anchorage-independent than for surface growth. Mesothelial cells are unable to divide at all in semi-solid medium without added EGF or with less than 2% serum, whereas they grow slowly but progressively in surface culture under such conditions. In semi-solid medium containing 20% serum and HC, mesothelial cells are stimulated to divide by the addition of as little as 30 pg/ml purified EGF. Human urine or male mouse plasma could substitute for purified EGF, yielding growth commensurate with the levels of EGF in these biological fluids previously measured by others using radioreceptor and radioimmune assays. Thus growth of mesothelial cells in semi-solid medium can serve as a highly sensitive assay of EGF biological activity which is unaffected by the presence of serum proteins. In addition, our results demonstrate that fetal calf serum does not provide mitogenic levels of EGF to cultured cells, raising the question of the identity of plasma and serum mitogens.
本实验室最近报道,正常人间皮细胞除了需要胎牛血清和一种复杂的限定培养基成分外,还需要表皮生长因子(EGF)和氢化可的松(HC),以便在表面培养中实现最佳生长。我们在此报告,这种正常细胞类型在半固体培养基中也能高效形成大菌落,但与表面生长相比,其在非锚定依赖性生长中对血清和EGF的需求更为严格。在不添加EGF或血清含量低于2%的情况下,间皮细胞在半固体培养基中完全无法分裂,而在这种条件下,它们在表面培养中生长缓慢但持续生长。在含有20%血清和HC的半固体培养基中,只需添加低至30 pg/ml的纯化EGF就能刺激间皮细胞分裂。人尿或雄性小鼠血浆可替代纯化的EGF,其生长情况与其他人先前使用放射受体和放射免疫测定法测得的这些生物体液中的EGF水平相当。因此,间皮细胞在半固体培养基中的生长可作为一种对EGF生物活性高度敏感的测定方法,该方法不受血清蛋白存在的影响。此外,我们的结果表明,胎牛血清不能为培养细胞提供有丝分裂水平的EGF,这就引发了血浆和血清有丝分裂原的身份问题。