Garner W L, Oyatsu Y, Zuccaro C, Rodriquez J L, Smith D J, Marcelo C L
Section of Plastic and Reconstructive Surgery, University of Michigan, Ann Arbor 48109, USA.
Prostaglandins Leukot Essent Fatty Acids. 1995 May;52(5):349-55. doi: 10.1016/0952-3278(95)90037-3.
Epidermal cell growth in culture, using the low calcium, low serum technique described by Boyce, is thought to induce rapid expansion by inducing an essential fatty acid (EFA) deficiency state. To determine the mechanisms whereby EFA deficiency induces increased epidermal cell growth, keratinocytes were passaged into medium without or with the addition of EFAs, 18:2(n-6), 20:4(n-6). The resulting populations were assayed for replication rate, differentiation, and plating efficiency. Supplemental EFAs significantly decrease keratinocyte culture expansion. This is evidenced by an increase in generation time, a decrease in thymidine incorporation, and a decrease in modeled replication rate. EFA supplementation also increased the expression of cornified cell envelopes. Serum-free medium induces EFA deficient keratinocytes that demonstrate increased replication and decreased differentiation. Restoration of EFAs reverses these changes. It may be possible to manipulate keratinocyte physiology using fatty acid modifications.
采用博伊斯描述的低钙、低血清技术在培养中培养表皮细胞,被认为是通过诱导必需脂肪酸(EFA)缺乏状态来诱导快速增殖。为了确定EFA缺乏诱导表皮细胞生长增加的机制,将角质形成细胞接种到不添加或添加EFA(18:2(n-6)、20:4(n-6))的培养基中。对所得细胞群体进行复制率、分化和接种效率检测。补充EFA显著降低角质形成细胞培养的增殖。这表现为代时增加、胸苷掺入减少以及模拟复制率降低。补充EFA还增加了角质化细胞包膜的表达。无血清培养基诱导EFA缺乏的角质形成细胞,其表现为复制增加和分化减少。恢复EFA可逆转这些变化。利用脂肪酸修饰来调控角质形成细胞生理学或许是可行的。