Kaur P, Li A
Division of Haematology, Hanson Center for Cancer Research, Institute for Medical and Veterinary Science, Adelaide, South Australia, Australia.
J Invest Dermatol. 2000 Mar;114(3):413-20. doi: 10.1046/j.1523-1747.2000.00884.x.
The basal layer of human epidermis is a heterogeneous population of proliferative and differentiating cells that can be divided into at least three functionally discrete compartments: keratinocyte stem cells, transit amplifying cells, and postmitotic differentiating cells. Basal cells adhere to the underlying basement membrane via integrins, and although decreased adhesion is a key event in epidermal differentiation, the specific role of particular integrins is poorly understood. We report here on the comparative expression and function of the beta1 versus alpha6beta4 integrins in keratinocyte stem cells, transit amplifying cells, and postmitotic differentiating cells of neonatal human foreskin epidermis. Adhesion assays demonstrate that both keratinocyte stem cells and transit amplifying cells comprise rapidly adhering cells that exhibit high levels of functional beta1 and alpha6beta4 integrins. Interestingly, a proportion of basal cells that have begun to differentiate in vivo within the basal layer as determined by their expression of the differentiation-specific markers K10 and involucrin also retain high levels of activated beta1 integrin, but downregulate alpha6beta4 expression selectively (termed alpha6dimbeta1bri). These cells also retain their adhesive capacity, indicating that induction of differentiation in vivo does not correlate with decreased beta1 integrin expression or function. We have previously reported on the use of alpha6 integrin in conjunction with a proliferation associated marker (10G7 ag) to separate keratinocyte stem cells (phenotype alpha6bri10G7dim) from other basal cells (Li et al. Proc Natl Acad Sci 95:3902-3907 1998). A comparison of the long-term proliferative potential of beta1bri10G7dim cells with alpha6bri10G7dim showed that selection of alpha6bri10G7dim allows the isolation of a purer fraction of keratinocyte stem cells.
人表皮的基底层是一群异质性的增殖和分化细胞,可分为至少三个功能上离散的区室:角质形成干细胞、过渡扩增细胞和有丝分裂后分化细胞。基底细胞通过整合素附着于下方的基底膜,尽管粘附力下降是表皮分化中的关键事件,但特定整合素的具体作用仍知之甚少。我们在此报告β1与α6β4整合素在新生儿包皮表皮的角质形成干细胞、过渡扩增细胞和有丝分裂后分化细胞中的比较表达和功能。粘附试验表明,角质形成干细胞和过渡扩增细胞均包含快速粘附细胞,这些细胞表现出高水平的功能性β1和α6β4整合素。有趣的是,根据分化特异性标志物K10和内披蛋白的表达确定,在体内基底层内已开始分化的一部分基底细胞也保留了高水平的活化β1整合素,但选择性地下调α6β4表达(称为α6低β1高)。这些细胞也保留了它们的粘附能力,表明体内分化的诱导与β1整合素表达或功能的降低无关。我们之前曾报道过使用α6整合素结合增殖相关标志物(10G7抗体)从其他基底细胞中分离角质形成干细胞(表型为α6高10G7低)(Li等人,《美国国家科学院院刊》95:3902 - 3907,1998)。β1高10G7低细胞与α6高10G7低细胞长期增殖潜力的比较表明,选择α6高10G7低可分离出更纯的角质形成干细胞组分。