Lan Wei, Liu De-Wu, Li Guo-Hai, Mao Yuan-Gui, Chen Hua, Yi Xian-Feng, Wang Lian-Qun, Peng Yan, Zhong Qing-Ling
Department of Burns and Rehabilitation, Guangdong Provincial Work Injury Rehabilitation Hospital, Guangzhou 510970, China.
Zhonghua Shao Shang Za Zhi. 2011 Feb;27(1):26-31.
To analyze expression characteristics of human skin epidermal stem cell at different developmental stages, and to explore its biological significance.
Health skin samples from 28-32 w fetuses (F group), 4-12 y children (C group), and 35-55 y adult (A group) were harvested, with 10 cases in each group. Epidermis were separated using trypsin digestion and EDTA, and human epidermal stem cells were isolated and purified with type IV collagen attachment method. The monoclonal antibody of integrin beta1 and keratin 19 were used for detection and identification of epidermal stem cells by immunohistochemical staining. Total RNA was extracted from above cells by Trizol one-step method, and were detected by formaldehyde denaturing agarose gel electrophoresis. Probes were prepared and hybridized into cDNA microarray for scanning fluorescent signals and analysis of images, with two-fold differential expression value for screening. Significantly up/down-regulated genes were selected for verification by real time RT-PCR.
By comparing expression profile between A and C groups, a total of 1808 genes with differential expression were detected, including 1089 up-regulated genes and 719 down-regulated genes, and they were classified into 128 categories. Among them, 1462 genes were known (found in GeneBank), 346 genes were unknown. A total of 4534 genes with differential expression were detected between C and F groups, in which 1783 genes were up-regulated and 2751 genes were down-regulated, and they were classified into 216 categories. Among them, 3577 genes were known (found in GeneBank), and 957 genes were unknown. There were 1104 genes with differential expression consistently detected in F, C and A groups, which were classified into 32 categories according to gene function. Among them, 94 genes were consistently up-regulated and 75 genes consistently down-regulated. Test results of real time RT-PCR were in accordance with above-mentioned results.
Gene expression profiles of epidermal stem cells cultured in vitro, harvested from fetuses, children, and adult, exhibit obvious difference. This may be closely related to different stages of proliferation and differentiation of human epidermal stem cell and self-repair ability of wound at different developmental stages.
分析人皮肤表皮干细胞在不同发育阶段的表达特征,探讨其生物学意义。
收集28 - 32周胎儿(F组)、4 - 12岁儿童(C组)和35 - 55岁成人(A组)的健康皮肤样本,每组10例。采用胰蛋白酶消化和EDTA分离表皮,用IV型胶原贴壁法分离纯化人表皮干细胞。用整合素β1和角蛋白19单克隆抗体通过免疫组织化学染色检测和鉴定表皮干细胞。用Trizol一步法从上述细胞中提取总RNA,通过甲醛变性琼脂糖凝胶电泳进行检测。制备探针并与cDNA微阵列杂交,扫描荧光信号并分析图像,以两倍差异表达值进行筛选。选择显著上调/下调的基因通过实时RT-PCR进行验证。
比较A组和C组的表达谱,共检测到1808个差异表达基因,其中上调基因1089个,下调基因719个,分为128类。其中,1462个基因已知(在GeneBank中发现),346个基因未知。C组和F组之间共检测到4534个差异表达基因,其中上调基因1783个,下调基因2751个,分为216类。其中,3577个基因已知(在GeneBank中发现),957个基因未知。在F、C和A组中一致检测到1104个差异表达基因,根据基因功能分为32类。其中,94个基因持续上调,75个基因持续下调。实时RT-PCR检测结果与上述结果一致。
从胎儿、儿童和成人中获取并体外培养的表皮干细胞基因表达谱存在明显差异。这可能与人表皮干细胞在不同发育阶段的增殖、分化以及不同发育阶段伤口的自我修复能力密切相关。