Radoja Nada, Gazel Alix, Banno Tomohiro, Yano Shoichiro, Blumenberg Miroslav
Department of Dermatology, New York University School of Medicine, New York, New York, USA.
Physiol Genomics. 2006 Oct 3;27(1):65-78. doi: 10.1152/physiolgenomics.00031.2006. Epub 2006 Jul 5.
In epidermal differentiation basal keratinocytes detach from the basement membrane, stop proliferating, and express a new set of structural proteins and enzymes, which results in an impermeable protein/lipid barrier that protects us. To define the transcriptional changes essential for this process, we purified large quantities of basal and suprabasal cells from human epidermis, using the expression of beta4 integrin as the discriminating factor. The expected expression differences in cytoskeletal, cell cycle, and adhesion genes confirmed the effective separation of the cell populations. Using DNA microarray chips, we comprehensively identify the differences in genes expressed in basal and differentiating layers of the epidermis, including the ECM components produced by the basal cells, the proteases in both the basal and suprabasal cells, and the lipid and steroid metabolism enzymes in suprabasal cells responsible for the permeability barrier. We identified the signaling pathways specific for the two populations and found two previously unknown paracrine and one juxtacrine signaling pathway operating between the basal and suprabasal cells. Furthermore, using specific expression signatures, we identified a new set of late differentiation markers and mapped their chromosomal loci, as well as a new set of melanocyte-specific markers. The data represent a quantum jump in understanding the mechanisms of epidermal differentiation.
在表皮分化过程中,基底角质形成细胞从基底膜脱离,停止增殖,并表达一组新的结构蛋白和酶,这会形成一个保护我们的不可渗透的蛋白质/脂质屏障。为了确定这一过程所必需的转录变化,我们以β4整合素的表达作为区分因子,从人表皮中纯化出大量的基底细胞和基底上层细胞。细胞骨架、细胞周期和黏附基因中预期的表达差异证实了细胞群体的有效分离。使用DNA微阵列芯片,我们全面鉴定了表皮基底层和分化层中基因表达的差异,包括基底细胞产生的细胞外基质成分、基底细胞和基底上层细胞中的蛋白酶,以及基底上层细胞中负责渗透屏障的脂质和类固醇代谢酶。我们确定了这两种细胞群体特有的信号通路,并发现了两条以前未知的旁分泌信号通路和一条在基底细胞和基底上层细胞之间起作用的近分泌信号通路。此外,利用特定的表达特征,我们鉴定出一组新的晚期分化标志物并绘制了它们的染色体位点,以及一组新的黑素细胞特异性标志物。这些数据代表了我们在理解表皮分化机制方面的巨大飞跃。