Hameedaldeen Alhassan, Liu Jian, Batres Angelika, Graves Gabrielle S, Graves Dana T
School of Dental Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Stomatology, the 4th Hospital of Hebei Medical University, Shijiazhuang 050011, China.
Int J Mol Sci. 2014 Sep 15;15(9):16257-69. doi: 10.3390/ijms150916257.
Re-epithelialization is a complex process that involves migration and proliferation of keratinocytes, in addition to the production of cytokines and growth factors that affect other cells. The induction of transcription factors during these processes is crucial for successful wound healing. The transcription factor forkhead boxO-1 (FOXO1) has recently been found to be an important regulator of wound healing. In particular, FOXO1 has significant effects through regulation of transforming growth factor-beta (TGF-β) expression and protecting keratinocytes from oxidative stress. In the absence of FOXO1, there is increased oxidative damage, reduced TGF-β1 expression, reduced migration and proliferation of keratinocytes and increased keratinocytes apoptosis leading to impaired re-epithelialization of wounds.
再上皮化是一个复杂的过程,除了产生影响其他细胞的细胞因子和生长因子外,还涉及角质形成细胞的迁移和增殖。在这些过程中诱导转录因子对于伤口的成功愈合至关重要。转录因子叉头框O-1(FOXO1)最近被发现是伤口愈合的重要调节因子。特别是,FOXO1通过调节转化生长因子-β(TGF-β)的表达以及保护角质形成细胞免受氧化应激而发挥显著作用。在缺乏FOXO1的情况下,氧化损伤增加,TGF-β1表达降低,角质形成细胞的迁移和增殖减少,角质形成细胞凋亡增加,导致伤口再上皮化受损。