Daniel M R
Br J Cancer. 1970 Dec;24(4):712-8. doi: 10.1038/bjc.1970.85.
Embryonic chick epidermis, if cultured for 4 days on a TH millipore filter overlying certain malignant dermal fibroblasts, shows abnormalities ranging from complete degeneration to hypertrophy and abnormal differentiation. The effect of the tumour cells is prevented if the thickness of the filter is doubled, to 50 μm., but not if a 25 μm.-thick membrane is coated with a thin collagen gel. When a semipermeable membrane is interposed between the cells and the epidermis, the latter does not degenerate, but keratinizes without showing the usual stages of differentiation.The malignant cells sometimes cause hypertrophy of the epidermis when cultured beneath the dermis of intact skin, but have no effect when grown on the peridermal surface of this tissue or of isolated epidermis.Freeze- or heat-killed dermal cells, whether normal or malignant, provide an unsuitable substratum for epidermal survival, possibly due to adsorption of intracellular constituents on to their surfaces.IT IS SUGGESTED THAT THE MALIGNANT FIBROBLASTS EXAMINED PRODUCE AT LEAST TWO SUBSTANCES HAVING AN EFFECT ON EPIDERMIS: one of small molecular size affecting differentiation, and a toxic macromolecule. A growth-promoting substance may also be produced by the cells of one subline.
如果将鸡胚表皮在覆盖某些恶性真皮成纤维细胞的TH微孔滤膜上培养4天,会出现从完全退化到肥大及异常分化等各种异常情况。如果将滤膜厚度加倍至50μm,肿瘤细胞的这种作用就会被阻止,但如果在25μm厚的膜上涂上一层薄的胶原凝胶则不会。当在细胞和表皮之间插入半透膜时,表皮不会退化,但会角化,且不显示通常的分化阶段。恶性细胞在完整皮肤的真皮下方培养时有时会导致表皮肥大,但在该组织或分离表皮的表皮表面生长时则没有影响。无论是正常还是恶性的经冷冻或加热杀死的真皮细胞,都不是表皮存活的合适基质,这可能是由于细胞内成分吸附到了它们的表面。有人认为,所检测的恶性成纤维细胞至少产生两种对表皮有影响的物质:一种是小分子大小的影响分化的物质,以及一种有毒的大分子。一个亚系的细胞也可能产生一种生长促进物质。