Gilchrest B A, Calhoun J K, Maciag T
J Cell Physiol. 1982 Aug;112(2):197-206. doi: 10.1002/jcp.1041120207.
Using a serum-free system, we have investigated the influence of human fibronectin (HFN) and selected growth factors (GF) on the attachment and growth of normal human keratinocytes in vitro. Single-cell suspensions of keratinocytes from near-confluent primary plates, plated on 5-10 microgram/cm2 HFN, showed approximately 30-40% attachment after 2-24 hours of incubation at 37 degrees C, compared with 4-6% attachment on uncoated platic plates. Percentage of attached cells was independent of seed density, tissue donor age, in vitro culture age, or medium composition, while subsequent cellular proliferation was strongly dependent on these factors. Keratinocytes grown on an adequate HFN matrix in a previously described hormone-supplemented medium (Maciag et al., 1981a) achieved four to eight population doubling over 7-12 days at densities greater than or equal to 104 cell/cm2. Removal of most GF individually from the medium had little or no effect on growth, while removal of epidermal growth factor (EGF) alone reduced growth by 30-35% and removal of bovine brain extract (BE) alone reduced growth by approximately 90%. Conversely, EGF alone in basal medium supported approximately 10% control growth, BE alone supported 30-40% control growth, and the combination of EGF and BE approximately 70%. In addition to its major effect on proliferation in this system, BE was necessary to preserve normal keratinocyte morphology and protein production. These findings expand earlier observations that HFN facilitates keratinocyte attachment in vitro and that a brain-derived extract can exert a major positive influence on cultured keratinocytes.
我们使用无血清系统,研究了人纤连蛋白(HFN)和选定生长因子(GF)对正常人角质形成细胞体外附着和生长的影响。来自接近汇合的原代培养板的角质形成细胞单细胞悬液,接种在5 - 10微克/平方厘米的HFN上,在37℃孵育2 - 24小时后显示约30 - 40%的附着率,相比之下,未包被的塑料培养板上的附着率为4 - 6%。附着细胞的百分比与接种密度、组织供体年龄、体外培养时间或培养基成分无关,而随后的细胞增殖则强烈依赖于这些因素。在先前描述的添加激素的培养基(Maciag等人,1981a)中,在合适的HFN基质上生长的角质形成细胞,在密度大于或等于104个细胞/平方厘米时,7 - 12天内实现了4至8次群体倍增。从培养基中单独去除大多数生长因子对生长几乎没有影响,而单独去除表皮生长因子(EGF)使生长降低30 - 35%,单独去除牛脑提取物(BE)使生长降低约90%。相反,基础培养基中单独的EGF支持约10%的对照生长,单独的BE支持30 - 40%的对照生长,EGF和BE的组合支持约70%的对照生长。除了对该系统中的增殖有主要作用外,BE对于维持正常角质形成细胞的形态和蛋白质产生也是必需的。这些发现扩展了早期的观察结果,即,即HFN促进角质形成细胞的体外附着,并且一种脑源性提取物可对培养的角质形成细胞产生重大的积极影响。