Braun Susanne, Hanselmann Christine, Gassmann Marcus G, auf dem Keller Ulrich, Born-Berclaz Christiane, Chan Kaimin, Kan Yuet Wai, Werner Sabine
Institute of Cell Biology, Department of Biology, ETH Zürich, Hönggerberg, CH-8093 Zürich, Switzerland.
Mol Cell Biol. 2002 Aug;22(15):5492-505. doi: 10.1128/MCB.22.15.5492-5505.2002.
Keratinocyte growth factor (KGF) is a potent mitogen for epithelial cells, and it promotes survival of these cells under stress conditions. In a search for KGF-regulated genes in keratinocytes, we identified the gene encoding the transcription factor NF-E2-related factor 2 (Nrf2). Nrf2 is a key player in the cellular stress response. This might be of particular importance during wound healing, where large amounts of reactive oxygen species are produced as a defense against invading bacteria. Therefore, we studied the wound repair process in Nrf2 knockout mice. Interestingly, the expression of various key players involved in wound healing was significantly reduced in early wounds of the Nrf2 knockout animals, and the late phase of repair was characterized by prolonged inflammation. However, these differences in gene expression were not reflected by obvious histological abnormalities. The normal healing rate appears to be at least partially due to an up-regulation of the related transcription factor Nrf3, which was also identified as a target of KGF and which was coexpressed with Nrf2 in the healing skin wound. Taken together, our results reveal novel roles of the KGF-regulated transcription factors Nrf2 and possibly Nrf3 in the control of gene expression and inflammation during cutaneous wound repair.
角质形成细胞生长因子(KGF)是一种有效的上皮细胞促分裂原,在应激条件下可促进这些细胞的存活。在寻找角质形成细胞中KGF调节的基因时,我们鉴定出了编码转录因子NF-E2相关因子2(Nrf2)的基因。Nrf2是细胞应激反应中的关键因子。这在伤口愈合过程中可能尤为重要,因为此时会产生大量活性氧以抵御入侵细菌。因此,我们研究了Nrf2基因敲除小鼠的伤口修复过程。有趣的是,在Nrf2基因敲除动物的早期伤口中,参与伤口愈合的各种关键因子的表达显著降低,修复后期的特征是炎症持续时间延长。然而,这些基因表达的差异并未表现为明显的组织学异常。正常的愈合速度似乎至少部分归因于相关转录因子Nrf3的上调,Nrf3也被鉴定为KGF的靶标,且在愈合的皮肤伤口中与Nrf2共表达。综上所述,我们的研究结果揭示了KGF调节的转录因子Nrf2以及可能的Nrf3在皮肤伤口修复过程中控制基因表达和炎症方面的新作用。