Published: September 3rd, 2016
House Ear Institute-Organ of Corti 1 (HEI-OC1) is one of the few mouse auditory cell lines currently available for research purposes. This protocol describes how to work with HEI-OC1 cells to investigate the cytotoxic effects of pharmacological drugs as well as functional properties of inner ear proteins.
HEI-OC1 is one of the few mouse auditory cell lines available for research purposes. Originally proposed as an in vitro system for screening of ototoxic drugs, these cells have been used to investigate drug-activated apoptotic pathways, autophagy, senescence, mechanism of cell protection, inflammatory responses, cell differentiation, genetic and epigenetic effects of pharmacological drugs, effects of hypoxia, oxidative and endoplasmic reticulum stress, and expression of molecular channels and receptors. Among other several important markers of cochlear hair cells, HEI-OC1 cells endogenously express prestin, the paradigmatic motor protein of outer hair cells. Thus, they can be very useful to elucidate novel functional aspects of this important auditory protein. HEI-OC1 cells are very robust, and their culture usually does not present big complications. However, they require some special conditions such as avoiding the use of common anti-bacterial cocktails containing streptomycin or other antibiotics as well as incubation at 33 °C to stimulate cell proliferation and incubation at 39 °C to trigger cell differentiation. Here, we describe how to culture HEI-OC1 cells and how to use them in some typical assays, such as cell proliferation, viability, death, autophagy and senescence, as well as how to perform patch-clamp and non-linear capacitance measurements.
House Ear Institute-Organ of Corti 1 (HEI-OC1) cells are derived from the auditory organ of a transgenic mouse 1,2. Incubation of any cell from this transgenic mouse at 33 °C/10% CO2 (permissive conditions) induces expression of an immortalizing gene that triggers de-differentiation and accelerated proliferation; moving the cells to 39 °C/5% CO2 (non-permissive conditions) lead to decreased proliferation, differentiation and, at least in the case of HEI-OC1, cell death 2,3.
HEI-OC1 cells were cloned and characterized in our laboratory over a decade ago, and initial studies indicated that....
1. Cell Culture
Note: All cell culturing protocols must be performed using proper cell culture techniques (for reference see the first 3 Chapters of Cell Biology: A Laboratory Handbook, Volume I 10). HEI-OC1 cells do not require any additional coating or treatment of the cell culture dishes for proper adherence and growth. Very important: do not use glassware dishes for cell culture purposes; the phenotype and biological response of the cells to pharmacological drugs will change (G Ka.......
In a couple of recent publications we reported a comprehensive set of studies aimed at evaluating the response of HEI-OC1 cells to several commonly used pharmacological drugs as well as investigating prestin function 8,9. In these studies we made use of all the protocols described in the previous sections.
One of the results of these previous studies was that HEI-OC1 cells cultured at non-permissive conditions (39 .......
In this report we describe how to culture HEI-OC1 cells and use them to evaluate mechanisms of drug-induced cytotoxicity and to investigate functional properties of prestin, the molecular motor of cochlear OHCs. The technical procedures, however, are general enough to be easily adapted to different studies.
All the protocols described here require the correct use of well-established cell culture techniques 10. Just like with any other cell line, working with HEI-OC1 cells requires a.......
This work was supported by NIH Grants R01-DC010146 and R01-DC010397. Its content is solely the responsibility of the authors and does not necessarily represent the official view of the National Institutes of Health.....
|ALL THE ASSAY KITS, EQUIPMENTS
|Class II Biological Safety cabinet
|The Baker Company
|AND COMPANIES INDICATED IN THE
|PREVIOUS 2 COLUMNS ARE ONLY
|EXAMPLES, AND ANY OTHER SIMILAR
|PRODUCT COULD BE USED.
|Cellometer Auto T4
|Two (2) Cell incubators, one at 33°C/10% CO2 and other at 39°C/5% CO2
|Cell culture dishes, PS, 100 x 20 mm with vents
|Cell culture dishes , PS, 60 x 15 mm with vents
|Cellstar tissue culture flasks 250 mL
|Cellstar tissue cultur flasks 550 mL
|6 well cell culture plate, with lid-Cellstar
|Microtest Tissue culture plate, 96 well,flat bottom with lid
|Micro-Assay-Plate, Chimmey, 96-well white,clear botton
|50 ml Polypropylene conical tube with cap Cellstars
|15 ml Polypropylene conical tubes with cap-Cellstars
|PBS pH 7.4 (1X)
|Dulbecco’s Modified Eagle’s Medium (DMEM)
|Fetal bovine serum (FBS)
|Leibovitz's L-15 Medium, no phenol red
|TACS MTT Cell Proliferation Assay Kit
|Caspase-Glo 3/7 Assay kit
|BrdU Cell Proliferation Assay Kit
|Non-enzymatic cell dissociation solution
|Cell-Tox Green Cytotoxicity Assay Kit
|With 488 nm excitation (blue laser)
|Digital Blot Scanner
|Electrophoresis and Blotting Unit
|Spectra Max 5 Plate Reader with Soft Max Pro 5.2 Software
|Puller for preparing patch electrodes
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