Basal cell adhesion to a culture substratum controls the polarized spatial organization of human epidermal keratinocytes into proliferating basal and terminally differentiating suprabasal populations.

Epithelial cell biology Pub Date : 1993-01-01
Y Poumay, F Boucher, M Leclercq-Smekens, A Degen, R Leloup
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Abstract

The contribution of adhesion to an extracellular matrix in the polarized spatial organization of keratinocytes was studied in dispase-detached cultures stored as floating sheets. Proliferating and terminally differentiating cell populations were, therefore, localized on tissue sections by their DNA-synthesizing ability and involucrin immunostaining, respectively. A progressive reorganization was induced from superposed proliferating and differentiating layers into clusters exhibiting differentiating cells on the outside. Measurements of proliferation and terminal differentiation in detached cultures revealed the progressive disappearance of proliferating cells, followed by an increase in involucrin-positive cells. Attempts to block the spatial reorganization by the addition of components of the extracellular matrix remained unsuccessful. These results suggest that basal anchorage is responsible for the superposition of proliferating and differentiating cells in keratinocyte cultures. They afford new arguments for the induction of terminal differentiation in non-adhesive keratinocytes which exhibit a concomitant modification of cell shape.

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基底细胞与培养基质的粘附控制着人表皮角质形成细胞的极化空间组织,使其增殖为基底细胞和末梢分化的基底上细胞群。
在作为浮片储存的分离培养物中,研究了在角化细胞的极化空间组织中粘附到细胞外基质的贡献。因此,通过dna合成能力和天花素免疫染色,分别在组织切片上定位增殖和终末分化细胞群。从增殖和分化层叠加成集群,诱导渐进重组,外部显示分化细胞。在离体培养中对增殖和终末分化的测量显示,增殖细胞逐渐消失,随后是involucrin阳性细胞的增加。通过添加细胞外基质成分来阻止空间重组的尝试仍然不成功。这些结果表明,基底锚定在角化细胞培养中负责增殖和分化细胞的叠加。它们为非粘附性角质形成细胞的终末分化诱导提供了新的论据,这些细胞表现出伴随的细胞形状的改变。
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