Department of Surgery, School of Medicine, University of California, San Diego, CA, United States.
Department of Otolaryngology, School of Medicine, University of California, San Diego, CA, United States.
Front Cell Infect Microbiol. 2022 Feb 23;12:823714. doi: 10.3389/fcimb.2022.823714. eCollection 2022.
Otitis media (OM), the most common childhood illness, can be caused by bacterial and/or viral infection. Hyperplasia of the middle ear (ME) mucosa is an important component of OM that contributes to its deleterious sequelae. Our previous research revealed that ME mucosal hyperplasia in bacterially induced OM was associated with expression of the heparin-binding epidermal growth factor (HB-EGF) gene, and that HB-EGF induced the proliferation of ME mucosal explants in culture. We used single-cell RNA-Seq to identify ME cells that express and related genes involved in mediating responses to this factor. To determine the degree to which a viral infection might induce mucosal hyperplasia, and to assess the role of HB-EGF in hyperplasia , we used, Poly(I:C) to simulate a ME viral infection, Western blotting to confirm ME protein expression, and a specific inhibitor to block the effects of HB-EGF during OM. Genes for HB-EGF and its receptor were expressed in the ME primarily by epithelial, stromal and endothelial cells. Poly(I:C) induced prominent ME mucosal hyperplasia, peaking two days after ME injection. Immunostaining revealed that cleavage of proHB-EGF into its soluble form (sHB-EGF) was strongly induced in response to Poly(I:C). Inhibition of the sHB-EGF receptor dramatically reduced the hyperplastic response of the mucosa. The results demonstrate that a synthetic analog of viral double-stranded RNA interaction can induce OM including a strong proliferative response of the ME mucosa, independent of bacteria. They also indicate that HB-EGF is the dominant growth factor responsible for ME mucosal hyperplasia .
中耳炎(OM)是最常见的儿童疾病,可由细菌和/或病毒感染引起。中耳(ME)黏膜增生是 OM 的一个重要组成部分,导致其不良后果。我们之前的研究表明,细菌诱导的 OM 中 ME 黏膜增生与肝素结合表皮生长因子(HB-EGF)基因的表达有关,并且 HB-EGF 诱导 ME 黏膜外植体在培养中的增殖。我们使用单细胞 RNA-Seq 鉴定表达 和相关基因的 ME 细胞,这些基因参与介导对该因子的反应。为了确定病毒感染可能诱导黏膜增生的程度,并评估 HB-EGF 在增生中的作用 ,我们使用 Poly(I:C)模拟 ME 病毒感染,Western blot 确认 ME 蛋白表达,并用特定抑制剂在 OM 期间阻断 HB-EGF 的作用。HB-EGF 和其受体的基因主要由上皮细胞、基质细胞和内皮细胞在 ME 中表达。Poly(I:C) 诱导了明显的 ME 黏膜增生,在 ME 注射后两天达到峰值。免疫染色显示,proHB-EGF 被强烈切割成其可溶性形式(sHB-EGF),以响应 Poly(I:C)。sHB-EGF 受体的抑制显著降低了黏膜的增生反应。结果表明,合成的病毒双链 RNA 相互作用类似物可以诱导 OM,包括 ME 黏膜的强烈增殖反应,与细菌无关。它们还表明,HB-EGF 是负责 ME 黏膜增生的主要生长因子。