Staiano-Coico L, Higgins P J
Department of Surgery, Cornell University Medical College, New York, New York 10021.
Exp Cell Res. 1992 Jul;201(1):126-36. doi: 10.1016/0014-4827(92)90356-d.
Normal human keratinocytes (NHK) in submerged culture were used to assess mechanisms associated with in vitro exposure to known stimulators (sodium butyrate; NaB) and inhibitors (fibronectin; FN) of NHK maturation. A multiparameter approach was used to define cell types generated under a range of growth conditions. Differentiation induced in response to NaB occurred through a series of morphologically distinct phenotypes and culminated in the formation of enucleate-cornified envelopes. Two-dimensional electrophoresis provided a limited database to evaluate global changes in cellular protein composition as a function of induced differentiation. Proteins were identified that characterized predominantly basal cell cultures, NaB-treated cells, and fully differentiated NHKs. Growth of NHKs on FN suppressed both spontaneous and NaB-directed maturation and inhibited maximal expression of protein changes associated with the differentiated state. Thus, the composition of the extracellular matrix can modulate (at both the morphologic and protein levels) the response of basal NHKs to a potent differentiation-inducing agent. Abrogation of NHK maturation by FN was not due to adverse effects on cellular metabolism, abortive differentiation, or altered timing of induced differentiation. FN appears to exert its suppressive effect by either maintaining an early stem cell phenotype which is poorly competent for terminal maturation or attenuating an as yet unknown aspect of the NaB-initiated differentiation cascade.
在浸没培养中使用正常人角质形成细胞(NHK)来评估与体外暴露于已知的NHK成熟刺激剂(丁酸钠;NaB)和抑制剂(纤连蛋白;FN)相关的机制。采用多参数方法来定义在一系列生长条件下产生的细胞类型。对NaB的反应诱导的分化通过一系列形态学上不同的表型发生,并最终形成无核角质化包膜。二维电泳提供了一个有限的数据库,以评估作为诱导分化函数的细胞蛋白质组成的整体变化。鉴定出了主要表征基底细胞培养物、NaB处理的细胞和完全分化的NHK的蛋白质。NHK在FN上的生长抑制了自发和NaB导向的成熟,并抑制了与分化状态相关的蛋白质变化的最大表达。因此,细胞外基质的组成可以(在形态学和蛋白质水平上)调节基底NHK对强效分化诱导剂的反应。FN对NHK成熟的废除不是由于对细胞代谢、流产分化或诱导分化时间改变的不利影响。FN似乎通过维持对终末成熟能力差的早期干细胞表型或减弱NaB启动的分化级联反应的一个未知方面来发挥其抑制作用。