Wilkins L, Gilchrest B A, Szabo G, Weinstein R, Maciag T
J Cell Physiol. 1985 Mar;122(3):350-61. doi: 10.1002/jcp.1041220304.
Cell culture conditions for the selective growth and serial propagation of normal human melanocytes from epidermal tissue are described. In addition to the presence of 2% fetal bovine serum, the human melanocyte cell culture environment contains the following growth factor supplements: epidermal growth factor (10 ng/ml), triiodothyronine (10(-9) M), hydrocortisone, (5 X 10(-5) M), insulin (10 micrograms/ml), transferrin (10 micrograms/ml), 7S nerve growth factor (100 ng/ml) cholera toxin (10(-10) M), and bovine brain extract (150 micrograms/ml). The ability to establish selectively the human melanocyte in vitro has been attributed to the contrast between human epidermal keratinocytes and melanocytes for attachment to fibronectin, while the growth of the human melanocyte has been attributed to the mitogenic activity of the growth factor-supplemented medium. Human melanocytes can be cultivated for at least 15 cumulative population doublings and are capable of [3H]-Dopa incorporation. The growth factor-supplemented medium contains a neutral extract from bovine brain that is a potent source of a human melanocyte mitogen. The biological activity of melanocyte growth factor is described as a heat and alkaline-labile mitogen with an estimated molecular weight of 30,000 by gel exclusion chromatography and a weakly cationic isoelectric point. The mitogen is capable of stimulating the growth of quiescent populations of human melanocytes in vitro. The ability to isolate and propagate normal human melanocytes in vitro permitted an examination of the expression of fibronectin and tissue plasminogen activator. Human epidermal melanocytes established in culture do not contain either tissue plasminogen activator or fibronectin. In contrast, human melanoma cell lines contain immunologically detectable fibronectin and tissue plasminogen activator. The absence of tissue plasminogen activator and fibronectin in normal human melanocytes also occurs under conditions of co-cultivation with human melanoma cells. These contrasts between normal human melanocytes and human melanoma cells may be relevant to the metastatic capabilities of human melanoma.
本文描述了从表皮组织中选择性培养正常人黑素细胞并进行连续传代的细胞培养条件。除了含有2%胎牛血清外,人黑素细胞的细胞培养环境还包含以下生长因子补充剂:表皮生长因子(10 ng/ml)、三碘甲状腺原氨酸(10(-9) M)、氢化可的松(5×10(-5) M)、胰岛素(10微克/ml)、转铁蛋白(10微克/ml)、7S神经生长因子(100 ng/ml)、霍乱毒素(10(-10) M)和牛脑提取物(150微克/ml)。在体外选择性培养人黑素细胞的能力归因于人表皮角质形成细胞和黑素细胞在附着于纤连蛋白方面的差异,而人黑素细胞的生长则归因于补充了生长因子的培养基的促有丝分裂活性。人黑素细胞可以培养至少15次累积群体倍增,并能够掺入[3H]-多巴。补充了生长因子的培养基含有来自牛脑的中性提取物,它是一种有效的人黑素细胞有丝分裂原来源。黑素细胞生长因子的生物活性被描述为一种对热和碱不稳定的有丝分裂原,通过凝胶排阻色谱法估计其分子量为30,000,等电点为弱阳离子性。该有丝分裂原能够在体外刺激静止的人黑素细胞群体生长。在体外分离和培养正常人黑素细胞的能力使得能够检测纤连蛋白和组织纤溶酶原激活物的表达。培养的人表皮黑素细胞既不含有组织纤溶酶原激活物也不含有纤连蛋白。相比之下,人黑色素瘤细胞系含有可通过免疫检测到的纤连蛋白和组织纤溶酶原激活物。在与人黑色素瘤细胞共培养的条件下,正常人黑素细胞中也不存在组织纤溶酶原激活物和纤连蛋白。正常人黑素细胞和人黑色素瘤细胞之间的这些差异可能与人黑色素瘤的转移能力有关。