Holbrook K A, Hennings H
J Invest Dermatol. 1983 Jul;81(1 Suppl):11s-24s. doi: 10.1111/1523-1747.ep12540003.
Disaggregated epidermal cells, sheets of epidermis, and explants of partial and full-thickness skin have been grown in cell, organ, and explant cultures. Each type of epidermal sample has also been "cultured" as a graft on a living animal host. The extent of tissue-specific phenotypic expression by the epidermal cell varies with the type of culture and the culture conditions: medium, biologic and pharmacologic additives, substrate, cell density, pH, and temperature. Specific culture conditions can be chosen to select for certain phenotypic traits. In spite of the diversity of conditions that may be used for culture, keratinocytes in cell, explant, and organ cultures undergo a similar pattern of differentiation. They stratify and keratinize, but rarely express a complete program of keratinization. Many of the characteristics associated with this pattern of differentiation are also observed in fetal epidermis during development. In culture, normal tissue architecture is usually absent; cells organize in flattened, loosely associated layers, synthesize a different pattern of keratin polypeptides, form keratohyalin granules only sporadically, and rarely contain lamellar granules. Epidermal differentiation in explant and organ cultures can be evaluated in regions of the explant, epibolic zone, and outgrowth apron. The epidermis of the original explant undergoes hyperproliferation, degeneration, sloughing, and then regeneration of a thin tissue. The cells in the epithelial outgrowth zone stratify and differentiate almost identically with those in cell culture. Neogenesis of structures in the basement-membrane zone can be followed in all three regions of the explant culture. Sheets of epidermis or epidermal cells transplanted onto or into a host animal show the most complete expression of the epidermal phenotype. After a period of hyperplastic growth, the cell layers become established in a pattern nearly identical to that in vivo. A complete granular layer is formed and stratum corneum cells, which are structurally and biochemically equivalent to those in tissue, differentiate. In some instances, the epidermis reconstructed from cells or tissue is indistinguishable from adjacent host epidermis. Experiments that include serial transfer from one culture system to another demonstrate the plasticity of the epidermal cell and its ability to respond variously to its environment.
已在细胞培养、器官培养和外植体培养中培养了离散的表皮细胞、表皮片以及部分厚度和全厚度皮肤的外植体。每种类型的表皮样本也已作为移植物“培养”在活体动物宿主上。表皮细胞的组织特异性表型表达程度随培养类型和培养条件而变化:培养基、生物和药理添加剂、底物、细胞密度、pH值和温度。可以选择特定的培养条件来选择某些表型特征。尽管可用于培养的条件多种多样,但细胞培养、外植体培养和器官培养中的角质形成细胞经历相似的分化模式。它们分层并角质化,但很少表达完整的角质化程序。在发育过程中,胎儿表皮中也观察到许多与这种分化模式相关的特征。在培养中,通常不存在正常的组织结构;细胞组织成扁平、松散相连的层,合成不同模式的角蛋白多肽,仅偶尔形成透明角质颗粒,并且很少含有板层颗粒。外植体和器官培养中的表皮分化可在外植体、外包区和生长边缘区进行评估。原始外植体的表皮经历过度增殖、退化、脱落,然后再生出薄组织。上皮生长区的细胞分层和分化与细胞培养中的细胞几乎相同。在外植体培养的所有三个区域都可以追踪基底膜区结构的新生。移植到宿主动物上或植入宿主动物体内的表皮片或表皮细胞表现出表皮表型的最完整表达。经过一段增生性生长后,细胞层以与体内几乎相同的模式建立。形成完整的颗粒层,并且角质层细胞分化,其在结构和生化上与组织中的角质层细胞相当。在某些情况下,由细胞或组织重建的表皮与相邻的宿主表皮无法区分。包括从一种培养系统连续转移到另一种培养系统的实验证明了表皮细胞的可塑性及其对环境做出不同反应的能力。