17β-estradiol Attenuates the Middle Ear Inflammatory Response to Nontypeable Haemophilus influenzae

被引:0
|
作者
Khampang, Pawjai [1 ]
Samuels, Tina L. [1 ]
Blaine-Sauer, Simon [1 ]
Lucas, Julliette [1 ]
Yan, Ke [2 ]
Johnston, Nikki [1 ,3 ]
Kerschner, Joseph E. [1 ,3 ,4 ,5 ]
机构
[1] Med Coll Wisconsin, Dept Otolaryngol & Commun Sci, Milwaukee, WI USA
[2] Med Coll Wisconsin, Dept Quantitat Hlth Sci, Milwaukee, WI 53226 USA
[3] Med Coll Wisconsin, Dept Microbiol & Immunol, Milwaukee, WI USA
[4] Childrens Wisconsin, Milwaukee, WI USA
[5] Med Coll Wisconsin, 8701 Watertown Plank Rd, Milwaukee, WI 53226 USA
来源
LARYNGOSCOPE | 2024年 / 134卷 / 08期
关键词
17; beta-estradiol; estrogen; inflammatory cytokines; nontypeable Haemophilus influenza; otitis media; UTERINE EPITHELIAL-CELLS; INNATE IMMUNE FUNCTION; CHRONIC OTITIS-MEDIA; GEL-FORMING MUCINS; ESTROGEN-RECEPTOR; CYTOKINE RELEASE; GENE-EXPRESSION; SEX-DIFFERENCES; IN-VITRO; ESTRADIOL;
D O I
10.1002/lary.31343
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objectives 17 beta-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. Methods 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. Results 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). Conclusion 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.
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页码:3815 / 3819
页数:5
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