From the *Department of Ophthalmology; and †Allergy Research Center, Juntendo University School of Medicine, Tokyo, Japan.
Cornea. 2010 Nov;29 Suppl 1:S41-7. doi: 10.1097/ICO.0b013e3181ea9958.
To investigate the role of the epithelium in severe allergic conjunctivitis.
We first investigated the expression of protease-activated receptors (PARs) in cultured human conjunctival epithelial cells and fibroblasts by reverse transcription-polymerase chain reaction. Next, we examined whether mite allergen-stimulated cells release chemokines and whether physiological protease inhibitors such as secretory leukocyte protease inhibitor (SLPI) and α1-antitrypsin can inhibit their production. We also looked at the expression of thymic stromal lymphopoietin (TSLP) in giant papillae of patients with vernal keratoconjunctivitis and examined whether the as Toll-like receptor 3 ligand polyinosinic:polycytidylic acid (poly I:C) can induce expression of TSLP in cultured human conjunctival epithelial cells.
PAR 1, PAR2, and PAR3 were expressed in cultured human conjunctival epithelial cells and fibroblasts at mRNA level. These epithelial cells released interleukin (IL) 6 and IL-8, with an upregulation in their gene expression, in response to the serine protease activity of mite allergens. This response was inhibited by SLPI and α1-antitrypsin. Transforming growth factor β1 decreased the production of SLPI in corneal and conjunctival epithelial cells. TSLP was expressed in giant papillae epithelium in patients with vernal keratoconjunctivitis at mRNA and protein levels. Poly I:C induced expression of TSLP in cultured conjunctival epithelial cells at mRNA level. Costimulation with TSLP and IL-33 had a synergistic effect for IL-13 mRNA expression in cultured human mast cells.
Imbalance between protease of mite allergens and innate protease inhibitors of the epithelium may induce inflammation and disrupt barrier function. Viral infection may induce expression of TSLP via Toll-like receptors and release IL-33 by necrosis. These phenomena promote excessive allergic reactions; hence, the epithelium takes "center stage" in allergic conjunctivitis.
研究上皮细胞在严重过敏性结膜炎中的作用。
我们首先通过反转录-聚合酶链反应(RT-PCR)检测培养的人结膜上皮细胞和成纤维细胞中蛋白酶激活受体(PARs)的表达。接下来,我们研究了螨变应原刺激细胞是否释放趋化因子,以及生理蛋白酶抑制剂(如分泌型白细胞蛋白酶抑制剂[SLPI]和α1-抗胰蛋白酶)是否可以抑制其产生。我们还观察了胸腺基质淋巴细胞生成素(TSLP)在春季角结膜炎巨大乳头中的表达,并研究了 Toll 样受体 3 配体聚肌胞苷酸(poly I:C)是否可以诱导培养的人结膜上皮细胞表达 TSLP。
PAR1、PAR2 和 PAR3 在培养的人结膜上皮细胞和成纤维细胞中均在 mRNA 水平表达。这些上皮细胞在受到螨变应原的丝氨酸蛋白酶活性刺激后,IL-6 和 IL-8 的基因表达上调,导致其释放。该反应可被 SLPI 和α1-抗胰蛋白酶抑制。转化生长因子β1(TGF-β1)降低了角膜和结膜上皮细胞中 SLPI 的产生。春季角结膜炎患者的巨大乳头上皮细胞中表达 TSLP,mRNA 和蛋白水平均如此。poly I:C 可诱导培养的结膜上皮细胞中 TSLP 的 mRNA 表达。TSLP 与 IL-33 共刺激对培养的人肥大细胞中 IL-13 mRNA 的表达具有协同作用。
螨变应原的蛋白酶与上皮固有蛋白酶抑制剂之间的失衡可能会引起炎症并破坏屏障功能。病毒感染可能通过 Toll 样受体诱导 TSLP 的表达,并通过坏死释放 IL-33。这些现象促进了过度的过敏反应;因此,上皮细胞在过敏性结膜炎中处于“中心舞台”。