Department of Pharmacology, College of Korean Medicine, Kyung Hee University, Dongdaemun-gu, Seoul, Republic of Korea.
Department of Pharmacology, College of Korean Medicine, Kyung Hee University, Dongdaemun-gu, Seoul, Republic of Korea.
J Invest Dermatol. 2014 Oct;134(10):2521-2530. doi: 10.1038/jid.2014.198. Epub 2014 Apr 21.
Thymic stromal lymphopoietin (TSLP) is known to promote T helper type 2 cell-associated inflammation. Mast cells are major effector cells in allergic inflammatory responses. We noted that the population and maturation of mast cells were reduced in TSLP-deficient mice (TSLP-/-). Thus, we hypothesized that TSLP might affect mast cell development. We found that TSLP induced the proliferation and differentiation of mast cells from bone marrow progenitors. TSLP-induced mast cell proliferation was abolished by depletion of mouse double minute 2 (MDM2) and signal transducers and activators of transcription 6 (STAT6), as an upstream activator of MDM2. TSLP-/-, in particular, had a considerable deficit in the expression of MDM2 and STAT6. Also, the TSLP deficiency attenuated mast cell-mediated allergic reactions through the downregulation of STAT6 and MDM2. In an antibody microarray chip analysis, MDM2 expression was increased in atopic dermatitis patients. These observations indicate that TSLP is a factor for mast cell development, and that it aggravates mast cell-mediated immune responses.
胸腺基质淋巴细胞生成素(TSLP)已知可促进辅助性 T 细胞 2 型细胞相关炎症。肥大细胞是过敏炎症反应的主要效应细胞。我们注意到 TSLP 缺陷型小鼠(TSLP-/-)中的肥大细胞数量和成熟度降低。因此,我们假设 TSLP 可能影响肥大细胞的发育。我们发现 TSLP 可诱导骨髓祖细胞中的肥大细胞增殖和分化。通过耗尽鼠双微体 2(MDM2)和信号转导和转录激活因子 6(STAT6),作为 MDM2 的上游激活剂,可消除 TSLP 诱导的肥大细胞增殖。特别是,TSLP-/-在 MDM2 和 STAT6 的表达上存在相当大的缺陷。此外,通过下调 STAT6 和 MDM2,TSLP 缺乏可减弱肥大细胞介导的过敏反应。在抗体微阵列芯片分析中,特应性皮炎患者的 MDM2 表达增加。这些观察结果表明,TSLP 是肥大细胞发育的一个因素,并且它加重了肥大细胞介导的免疫反应。