Establishment of novel immortalized middle ear cell lines as models for otitis media

Author:

Blaine‐Sauer Simon1ORCID,Samuels Tina L.1ORCID,Khampang Pawjai1,Yan Ke2,McCormick Michael E.13ORCID,Chun Robert H.13ORCID,Harvey Steven A.134,Friedland David R.134ORCID,Johnston Nikki15,Kerschner Joseph E.13

Affiliation:

1. Department of Otolaryngology and Communication Sciences Medical College of Wisconsin Milwaukee Wisconsin USA

2. Department of Pediatrics Quantitative Health Sciences Medical College of Wisconsin Milwaukee Wisconsin USA

3. Children's Wisconsin Milwaukee Wisconsin USA

4. Froedtert Hospital Milwaukee Wisconsin USA

5. Department of Microbiology and Immunology Medical College of Wisconsin Milwaukee Wisconsin USA

Abstract

AbstractObjectiveOtitis media (OM) is among the most frequently diagnosed pediatric diseases in the US. Despite the significant public health burden of OM and the contribution research in culture models has made to understanding its pathobiology, a singular immortalized human middle ear epithelial (MEE) cell line exists (HMEEC‐1, adult‐derived). We previously developed MEE cultures from pediatric patients with non‐inflamed MEE (PCI), recurrent OM (ROM), or OM with effusion (OME) and demonstrated differences in their baseline inflammatory cytokine expression and response to stimulation with an OM‐relevant pathogen lysate and cytokines. Herein, we sought to immortalize these cultures and assess retention of their phenotypes.MethodsMEE cultures were immortalized via lentivirus encoding temperature‐sensitive SV40 T antigen. Immortalized MEE lines and HMEEC‐1 grown in monolayer were stimulated with non‐typeable Haemophilus influenzae (NTHi) lysate. Gene expression (TNFA, IL1B, IL6, IL8, MUC5AC, and MUC5B) was assessed by qPCR.ResultsSimilar to parental cultures, baseline cytokine expressions were higher in pediatric OM lines than in HMEEC‐1 and PCI, and HMEEC‐1 cells were less responsive to stimulation than pediatric lines.ConclusionImmortalized MEE lines retained the inflammatory expression and responsiveness of their tissues of origin and differences between non‐OM versus OM and pediatric versus adult cultures, supporting their value as novel in vitro culture models for OM.

Funder

Medical College of Wisconsin

National Institute on Deafness and Other Communication Disorders

Publisher

Wiley

Subject

General Medicine

Reference53 articles.

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1. PANEL 3: Otitis media animal models, cell culture, tissue regeneration & pathophysiology;International Journal of Pediatric Otorhinolaryngology;2024-01

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