Method Article

Three-dimensional Organotypic Cultures of Vestibular and Auditory Sensory Organs

DOI:

10.3791/57527

⸱

June 1st, 2018

In This Article

Summary

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Three-dimensional organotypic cultures of the murine utricle and cochlea in optically clear collagen I gels preserve innate tissue morphology, allow for mechanical stimulation through adjustment of matrix stiffness, and permit virus-mediated gene delivery.

Abstract

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The sensory organs of the inner ear are challenging to study in mammals due to their inaccessibility to experimental manipulation and optical observation. Moreover, although existing culture techniques allow biochemical perturbations, these methods do not provide a means to study the effects of mechanical force and tissue stiffness during development of the inner ear sensory organs. Here we describe a method for three-dimensional organotypic culture of the intact murine utricle and cochlea that overcomes these limitations. The technique for adjustment of a three-dimensional matrix stiffness described here permits manipulation of the elastic force opposing tissue growth. This method can therefore be used to study the role of mechanical forces during inner ear development. Additionally, the cultures permit virus-mediated gene delivery, which can be used for gain- and loss-of-function experiments. This culture method preserves innate hair cells and supporting cells and serves as a potentially superior alternative to the traditional two-dimensional culture of vestibular and auditory sensory organs.

Introduction

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The study of most aspects of mammalian organ development has been facilitated by in vitro systems. Two principal methods are now used for the culture of vestibular sensory organs: free-floating1 and adherent2 preparations. Both methods permit the investigation of hair cell vulnerabilities3 and regeneration1,4 in vitro. In addition, the developmental roles of the Notch5,6, Wnt7,8, and epidermal growth ....

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Protocol

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All methods described here have been approved by the Animal Care and Use Committees of Rockefeller University and of the University of Southern California.

1. (Optional) Preparation of Collagen I Solution from Mouse-tail Tendons

Note: Collagen I solutions are available commercially. Follow the manufacturer's instructions for gel preparation.

  1. Euthanize 5 - 10 young adult (3 - 5 weeks old) mice of any wild type strain with carbon dioxide in accordance with the protocol approved by the relevant Institutional Animal Care and Use Committee16. Collect the tails a....

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Results

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Vestibular and auditory sensory organs from embryonic ears, cultured in 40-Pa collagen I gels mimicking low stiffness embryonic conditions11, retain relatively normal three-dimensional structures (Figure 1) and maintain hair cells and supporting cells (Figure 2 and Figure 3). Although supporting cell density decreases by over 30% (Student's t-test: n = 4, p &.......

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Discussion

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The molecular signals that mediate growth and differentiation in the inner ear during development have been studied extensively5,6,7,8,9,10. However, evidence obtained from the utricular model system suggests that mechanical cues, sensed through cell junctions and the activation of Hippo signaling, also play an important role.......

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Disclosures

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The authors have nothing to disclose.

Acknowledgements

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We thank Dr. A. Jacobo, Dr. J. Salvi, and A. Petelski for their contributions to the original research on which this protocol is based. We also thank J. Llamas and W. Makmura for technical assistance and animal husbandry. We acknowledge NIDCD Training grant T32 DC009975, NIDCD grant R01DC015530, Robertson Therapeutic Development Fund, and the Caruso Family Foundation for funding. Finally, we acknowledge support from Howard Hughes Medical Institute, of which Dr. Hudspeth is an Investigator.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
#10 Surgical BladesMiltex4-110
#5 ForcepsDumont11252-20
100 mm Petri dishSigmaP5856-500EA
250 uL large orifice pipette tipsUSA Scientific1011-8406
30 mm glass-bottom Petri dishMatsunami Glass USA CorporationD35-14-1.5-U
4 well plateThermo Fisher Scientific176740
4-Hydroxytamoxifen SigmaH7904
60 mm Petri dishThermo Fisher Scientific123TS1
Acetic acid Sigma537020
Ad-GFPVector Biolabs1060
Anti-GFP, chicken IgY fractionInvitrogenA10262 
Anti-Myo7AProteus Biosciences25-6790
Anti-Sox2 Antibody (Y-17)Santa Cruzsc-17320
Bicinchoninic acid assayThermo Fisher Scientific23225
Click-iT EdU Alexa Fluor 647 Imaging KitThermo Fisher ScientificC10340
Collagenase IGibco17100017
D-glucoseSigmaG8270
DMEM/F12 Gibco11320033
Epidermal growth factorSigmaE9644
Fetal Bovine Serum (FBS)Thermo Fisher Scientific16140063
Fibroblast growth factorSigmaF5392
Flaming/Brown Micropipette PullerSutter InstrumentP-97
GlutamineSigmaG8540
HBSSGibco14025092
Hemocytometer DaiggerEF16034F
HEPESSigmaH4034
InsulinSigmaI3536
Iridectomy scissors Zepf Medical Instruments08-1201-10  
MicroinjectorNarishigeIM-6
NicotinamideSigmaN0636
PBS (10X), pH 7.4Gibco70011044
PBS (1X), pH 7.4Gibco10010023
Phenol Red pH indicator SigmaP4633 
Pure Ethanol, 200 ProofDecon Labs 2716
RFP antibodyChromoTek 5F8
Sodium bicarbonateSigmaS5761
Sodium hydroxideSigmaS8045
Sodium seleniteSigmaS5261
Tabletop vortex VWR97043-562
TransferrinSigmaT8158
Trypan blue SigmaT6146

References

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  1. Oesterle, E. C., Tsue, T. T., Reh, T. A., Rubel, E. W. Hair-cell regeneration in organ cultures of the postnatal chicken inner ear. Hear Res. 70 (1), 85-108 (1993).
  2. Meyers, J. R., Corwin, J. T. Shape change controls supporting cell proli....

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Tags

Three dimensional Organotypic CultureMurine Vestibular OrgansMurine Auditory OrgansCollagen Type One GelViral Gene DeliveryTissue Stiffness AdjustmentInner Ear DevelopmentHair Cell PreservationSupporting Cell AnalysisConfocal Microscopy Imaging

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