Department of Biomedicine & Health Sciences, The Catholic University of Korea, #222 Banpo-daero, Seocho-gu, Seoul 06591, Republic of Korea.
Department of Dermatology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, #222 Banpo-daero, Seocho-gu, Seoul 06591, Republic of Korea.
Int J Mol Sci. 2023 Dec 10;24(24):17322. doi: 10.3390/ijms242417322.
The yes-associated protein (YAP) of the Hippo pathway regulates a variety of target genes involved in cell proliferation, survival, and inflammation. YAP and transcription activator with a PDZ-binding motif (TAZ) proteins act as mediators of the inflammatory response. Still, their role in atopic dermatitis (AD)-particularly, the association with the nuclear factor kappa-B and Janus kinase (JAK)-signal transducer and activator of transcription (STAT) pathways-is not fully understood. In this study, we found that YAP, is upregulated in AD patients and NC/Nga mouse model of AD. In addition, inhibition of YAP significantly reduced epidermal cell proliferation by 58% and mast cell numbers by 51% and attenuated the upregulation of both Th1- and Th2-associated cytokines. Among the JAK-STAT family proteins, the expressions of JAK1 and JAK2 and those of STAT1, STAT2, and STAT3 were also downregulated. These findings may explain the role of YAP in AD and suggest YAP inhibitors as promising therapeutic agents for AD.
Hippo 通路中的 yes 相关蛋白(YAP)调节多种参与细胞增殖、存活和炎症的靶基因。YAP 和 PDZ 结合基序转录激活因子(TAZ)蛋白作为炎症反应的介质。然而,它们在特应性皮炎(AD)中的作用,特别是与核因子 kappa-B 和 Janus 激酶(JAK)-信号转导和转录激活因子(STAT)途径的关联,尚不完全清楚。在这项研究中,我们发现 YAP 在 AD 患者和 AD 的 NC/Nga 小鼠模型中上调。此外,抑制 YAP 可使表皮细胞增殖减少 58%,肥大细胞数量减少 51%,并减弱 Th1 和 Th2 相关细胞因子的上调。在 JAK-STAT 家族蛋白中,JAK1 和 JAK2 以及 STAT1、STAT2 和 STAT3 的表达也下调。这些发现可能解释了 YAP 在 AD 中的作用,并表明 YAP 抑制剂是 AD 的有前途的治疗药物。