Baden H P, Kubilus J, Macdonald M J
J Invest Dermatol. 1981 Jan;76(1):53-5. doi: 10.1111/1523-1747.ep12524875.
The ability of psoriatic fibroblasts to stimulate growth of epidermal cells was studied by comparing the capacity of murine 3T3 cells, normal fibroblasts and psoriatic fibroblasts to act as feeder layers for cultured normal human keratinocytes. 3T3 cells consistently gave shorter times to confluency than normal or psoriatic cells which were about the same. The SDS polyacrylamide gel electrophoretic pattern of the fibrous protein was identical irrespective of the feeder layer use. Psoriatic epidermal cells could be grown from single cell suspensions by using 10(-9) M cholera toxin in the medium. The cultured psoriatic keratinocytes grew identically to normal cells and made the same fibrous protein. The psoriatic keratinocytes also grew better on 3T3 cells than normal or psoriatic fibroblasts.
通过比较小鼠3T3细胞、正常成纤维细胞和银屑病成纤维细胞作为培养的正常人角质形成细胞饲养层的能力,研究了银屑病成纤维细胞刺激表皮细胞生长的能力。3T3细胞达到汇合的时间始终比正常或银屑病细胞短,而正常和银屑病细胞的时间大致相同。无论使用何种饲养层,纤维蛋白的SDS聚丙烯酰胺凝胶电泳图谱都是相同的。通过在培养基中使用10(-9)M霍乱毒素,银屑病表皮细胞可以从单细胞悬液中生长出来。培养的银屑病角质形成细胞与正常细胞生长情况相同,并产生相同的纤维蛋白。银屑病角质形成细胞在3T3细胞上的生长也比正常或银屑病成纤维细胞更好。