Department of Otolaryngology and Communication Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, U.S.A.
Department of Pediatrics Quantitative Health Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, U.S.A.
Laryngoscope. 2024 Aug;134(8):3815-3819. doi: 10.1002/lary.31343. Epub 2024 Feb 24.
17β-estradiol (E2) is a steroidal hormone with immunomodulatory functions that play a role in infectious and inflammatory diseases. E2 was recently identified as the leading upstream regulator of differentially expressed genes in a comparative RNA sequencing study of pediatric patients with otitis media (OM) versus OM-free counterparts and may therefore play a role in the inflammatory response to bacterial otopathogens during pediatric OM. This study examined the effect of E2 on bacterial-induced inflammatory cytokine expression in an in vitro pediatric OM model.
An immortalized middle ear (ME) epithelial cell line, ROM-SV40, was developed from a pediatric recurrent OM patient. The culture was exposed to E2 at physiological levels for 1-48 h prior to 6 h-stimulation with nontypeable Haemophilus influenzae (NTHi) whole cell lysate. TNFA, IL1B, IL6, and IL8 were assayed by qPCR and ELISA.
E2 pretreatment (24 h) abrogated NTHi induction of IL6; a longer pretreatment (1-10 nM, 48 h) abrogated IL1B induction (p < 0.05). E2 pretreatment (5 nM, 48 h) abrogated NTHi-induced IL8 secretion (p = 0.017).
E2 pretreatment partially rescued NTHi-induced cytokine production by ME epithelia. These data support a role for E2 in moderating the excessive inflammatory response to middle ear infection that contributes to OM pathophysiology.
NA Laryngoscope, 134:3815-3819, 2024.
17β-雌二醇(E2)是一种具有免疫调节功能的甾体激素,在感染和炎症性疾病中发挥作用。E2 最近在一项小儿中耳炎(OM)患者与无 OM 对照组的比较 RNA 测序研究中被确定为差异表达基因的主要上游调节剂,因此可能在小儿 OM 期间对细菌耳病原体的炎症反应中发挥作用。本研究通过体外小儿 OM 模型研究了 E2 对细菌诱导的炎症细胞因子表达的影响。
从一名小儿复发性 OM 患者中建立了永生化中耳(ME)上皮细胞系 ROM-SV40。在 6 小时非定型流感嗜血杆菌(NTHi)全细胞裂解物刺激前,将培养物用生理水平的 E2 预处理 1-48 小时。通过 qPCR 和 ELISA 测定 TNFA、IL1B、IL6 和 IL8。
E2 预处理(24 小时)阻断了 NTHi 诱导的 IL6;更长的预处理(1-10 nM,48 小时)阻断了 IL1B 的诱导(p<0.05)。E2 预处理(5 nM,48 小时)阻断了 NTHi 诱导的 IL8 分泌(p=0.017)。
E2 预处理部分挽救了 ME 上皮细胞中 NTHi 诱导的细胞因子产生。这些数据支持 E2 在调节中耳感染引起的过度炎症反应中的作用,该反应有助于 OM 病理生理学。
无。喉科学,134:3815-3819,2024。