Literature DB >> 26930622

HEI-OC1 cells as a model for investigating drug cytotoxicity.

Gilda Kalinec1, Pru Thein1, Channy Park1, Federico Kalinec2.   

Abstract

The House Ear Institute-Organ of Corti 1 (HEI-OC1) is one of the few, and arguable the most used, mouse auditory cell line available for research purposes. Originally proposed as an in vitro system for screening of ototoxic drugs, it has been used to investigate, among other topics, apoptotic pathways, autophagy and senescence, mechanism of cell protection, inflammatory responses, cell differentiation, effects of hypoxia, oxidative and endoplasmic reticulum stress, and expression of molecular channels and receptors. However, the use of different techniques with different goals resulted in apparent contradictions on the actual response of these cells to some specific treatments. We have now performed studies to characterize the actual response of HEI-OC1 cells to a battery of commonly used pharmacological drugs. We evaluated cell toxicity, apoptosis, viability, proliferation, senescence and autophagy in response to APAP (acetaminophen), cisplatin, dexamethasone, gentamicin, penicillin, neomycin, streptomycin, and tobramycin, at five different doses and two time-points (24 and 48 h), by flow cytometry techniques and caspase 3/7, MTT, Cytotoxicity, BrdU, Beclin1, LC3 and SA-β-galactosidase assays. We also used HEK-293 and HeLa cells to compare some of the responses of these cells to those of HEI-OC1. Our results indicate that every cell line responds to the each drug in a different way, with HEI-OC1 cells showing a distinctive sensitivity to at least one of the mechanisms under study. Altogether, our results suggest that the HEI-OC1 might be a useful model to investigate biological responses associated with auditory cells, including auditory sensory cells, but a careful approach would be necessary at the time of evaluating drug effects.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Autophagy; Cell death; Cell senescence; Cell viability; Cytotoxicity; HEI-OC1 cells; HEK-293 cells; HeLa cells

Mesh:

Substances:

Year:  2016        PMID: 26930622     DOI: 10.1016/j.heares.2016.02.019

Source DB:  PubMed          Journal:  Hear Res        ISSN: 0378-5955            Impact factor:   3.208


  39 in total

1.  Working with Auditory HEI-OC1 Cells.

Authors:  Gilda M Kalinec; Channy Park; Pru Thein; Federico Kalinec
Journal:  J Vis Exp       Date:  2016-09-03       Impact factor: 1.355

2.  Talaromyces australis and Penicillium murcianum pigment production in optimized liquid cultures and evaluation of their cytotoxicity in textile applications.

Authors:  Vicente A Hernández; Ángela Machuca; Isaac Saavedra; Daniel Chavez; Allisson Astuya; Carolina Barriga
Journal:  World J Microbiol Biotechnol       Date:  2019-10-12       Impact factor: 3.312

3.  Immunohistochemical localization of Nrf2 in the human cochlea.

Authors:  Kumiko Hosokawa; Seiji Hosokawa; Gail Ishiyama; Akira Ishiyama; Ivan A Lopez
Journal:  Brain Res       Date:  2018-07-05       Impact factor: 3.252

4.  Clinical and Genome-wide Analysis of Cisplatin-induced Tinnitus Implicates Novel Ototoxic Mechanisms.

Authors:  Omar El Charif; Brandon Mapes; Matthew R Trendowski; Heather E Wheeler; Claudia Wing; Paul C Dinh; Robert D Frisina; Darren R Feldman; Robert J Hamilton; David J Vaughn; Chunkit Fung; Christian Kollmannsberger; Taisei Mushiroda; Michiaki Kubo; Eric R Gamazon; Nancy J Cox; Robert Huddart; Shirin Ardeshir-Rouhani-Fard; Patrick Monahan; Sophie D Fossa; Lawrence H Einhorn; Lois B Travis; M Eileen Dolan
Journal:  Clin Cancer Res       Date:  2019-04-05       Impact factor: 12.531

5.  RIPOR2-mediated autophagy dysfunction is critical for aminoglycoside-induced hearing loss.

Authors:  Jinan Li; Chang Liu; Ulrich Müller; Bo Zhao
Journal:  Dev Cell       Date:  2022-09-15       Impact factor: 13.417

6.  The monofunctional platinum(II) compounds, phenanthriplatin and pyriplatin, modulate apoptosis signaling pathways in HEI-OC1 auditory hybridoma cells.

Authors:  Jerry D Monroe; Alexandra M Johnston; Michael E Smith
Journal:  Neurotoxicology       Date:  2020-05-13       Impact factor: 4.294

7.  The Development of a Nano-based Approach to Alleviate Cisplatin-Induced Ototoxicity.

Authors:  Mohammad N Kayyali; Andrew J Ramsey; Elizabeth M Higbee-Dempsey; Lesan Yan; Bert W O'Malley; Andrew Tsourkas; Daqing Li
Journal:  J Assoc Res Otolaryngol       Date:  2018-01-18

8.  Metabolic reprogramming of inner ear cell line HEI-OC1 after dexamethasone application.

Authors:  Michel Kather; Sabine Koitzsch; Bernhard Breit; Stefan Plontke; Bernd Kammerer; Arne Liebau
Journal:  Metabolomics       Date:  2021-05-24       Impact factor: 4.290

9.  A combinatorial approach to protect sensory tissue against cisplatin-induced ototoxicity.

Authors:  Nicole K Febles; Mark A Bauer; Bo Ding; Xiaoxia Zhu; Nathan D Gallant; Robert D Frisina
Journal:  Hear Res       Date:  2022-01-10       Impact factor: 3.208

10.  Differentiation of embryonic stem cells into a putative hair cell-progenitor cells via co-culture with HEI-OC1 cells.

Authors:  Nathaniel T Carpena; So-Young Chang; Celine D G Abueva; Jae Yun Jung; Min Young Lee
Journal:  Sci Rep       Date:  2021-07-06       Impact factor: 4.379

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