Isseroff R R, Chun K T, Rosenberg R M
Department of Dermatology, University of California, Davis School of Medicine 95616.
Br J Dermatol. 1989 Apr;120(4):503-10. doi: 10.1111/j.1365-2133.1989.tb01323.x.
Scaly skin occurs in 80-90% of patients who are hypothyroid, the pathogenesis of which is unknown. Since thyroid hormone (T3) affects growth and differentiation in other organs, we examined the effects of its absence on keratinocytes in vitro. Human neonatal foreskin keratinocytes were cultivated and second passage cells were switched to T3-depleted (-T3) medium at 50% confluence. Cells maintained in the -T3 medium demonstrated increased (1.5 fold) levels of the cross-linking enzyme transglutaminase and increased (1.5 fold) formation of cornified envelopes, when compared to keratinocytes maintained in medium containing physiologic levels (2 X 10(-9)M) of T3. Additionally, in the -T3 cultures, the level of the protease plasminogen activator (PA), an enzyme implicated in the process of shedding of cornified cells, was decreased 70-80% of that measured in +T3 media. Absence of T3 from keratinocyte culture-medium increased both the level of the enzyme responsible for cross-linking cornified envelope precursors and the rate of envelope formation in cultured cells. The decreased levels of PA observed in the -T3 cultures could result in decreased shedding of cornified cells. These alterations in the process of keratinocyte differentiation may explain the clinically observed scaliness associated with hypothyroidism in humans. The molecular mechanism by which T3 alters keratinocyte cornification is not yet known.
80% - 90%的甲状腺功能减退患者会出现皮肤鳞屑,其发病机制尚不清楚。由于甲状腺激素(T3)影响其他器官的生长和分化,我们在体外研究了其缺乏对角质形成细胞的影响。培养人新生儿包皮角质形成细胞,当细胞达到50%汇合度时,将第二代细胞换至不含T3的(-T3)培养基中。与在含有生理水平(2×10⁻⁹M)T3的培养基中培养的角质形成细胞相比,在-T3培养基中培养的细胞显示交联酶转谷氨酰胺酶水平增加(1.5倍),角质包膜形成增加(1.5倍)。此外,在-T3培养物中,参与角质化细胞脱落过程的蛋白酶纤溶酶原激活剂(PA)的水平降至在+T3培养基中测得水平的70% - 80%。角质形成细胞培养基中缺乏T3会增加负责交联角质包膜前体的酶的水平以及培养细胞中包膜形成的速率。在-T3培养物中观察到的PA水平降低可能导致角质化细胞脱落减少。角质形成细胞分化过程中的这些改变可能解释了临床上观察到的人类甲状腺功能减退相关的皮肤鳞屑。T3改变角质形成细胞角化的分子机制尚不清楚。