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The stria vascularis is vital to the generation of endocochlear potential. Here, we present the dissection of the adult mouse stria vascularis for single-nucleus sequencing or immunostaining.
Endocochlear potential, which is generated by the stria vascularis, is essential to maintain an environment conducive to appropriate hair cell mechanotransduction and ultimately hearing. Pathologies of the stria vascularis can result in a decreased hearing. Dissection of the adult stria vascularis allows for focused single-nucleus capture and subsequent single-nucleus sequencing and immunostaining. These techniques are used to study stria vascularis pathophysiology at the single-cell level.
Single-nucleus sequencing can be used in the setting of transcriptional analysis of the stria vascularis. Meanwhile, immunostaining continues to be useful in identifying specific populations of cells. Both methods require proper stria vascularis dissection as a prerequisite, which can prove to be technically challenging.
The cochlea consists of three fluid filled chambers, the scala vestibuli, scala media, and scala tympani. The scala vestibuli and scala tympani each contain perilymph, which has a high concentration of sodium (138 mM) and a low concentration of potassium (6.8 mM)1. The scala media contains endolymph, which has a high concentration of potassium (154 mM) and a low concentration of sodium (0.91 mM)1,2,3. This difference in ion concentration can be referred to as the endocochlear potential (EP), and is primarily generated by the movement of potassium ions ....
All animal experiments and procedures were performed according to protocols approved by the Animal Care and Use Committee of the National Institute of Neurological Diseases and Stroke and the National Institute on Deafness and Other Communication Disorders, National Institutes of Health. All experimental protocols were approved by the Animal Care and Use Committee of the National Institute of Neurological Diseases and Stroke and the National Institute on Deafness and Other Communication Disorders, National Institutes of .......
We present a method to isolate the SV to be used for either sNuc-Seq or immunostaining. The relevant anatomy (Figure 1) of the cochlea relative to the SV can help users better understand the organization of the SV and steps of the dissection protocol.
Each step of this microdissection of SV from a P30 mouse is detailed in the associated video, and snapshots of the key steps of this dissection and isolation of SV are presented in Figure 2
Prior to the advent of single-cell sequencing, many researchers used bulk tissue analysis, which only made it possible to analyze transcriptomes averaged across cells. In particular, single-cell and sNuc-Seq made it possible to isolate the transcriptome of a single cell or single nucleus, respectively32. In this instance, single-nucleus transcriptomes can be identified for marginal, intermediate, and basal cells, as well as spindle cells30. This enables the investigation of.......
This research was supported in part by the Intramural Research Program of the NIH, NIDCD to M.H. (DC000088)
....Name | Company | Catalog Number | Comments |
10-µm filter (Polyethylenterephthalat) | PluriSelect | #43-50010-01 | Filter tissue during sNuc-Seq |
18 x 18 mm cover glass | Fisher Scientific | 12-541A | Cover slip to mount SV |
30-µm filter (Polyethylenterephthalat) | PluriSelect | #43-50030-03 | Filter tissue during sNuc-Seq |
75 x 25 mm Superfrost Plus/Colorforst Plus Microslide | Daigger | EF15978Z | Microslide to mount SV on |
C57BL/6J Mice | The Jackson Laboratory | RRID: IMSR_JAX:000664 | General purpose mouse strain that has pigment more easily seen in the intermediate cells of the SV. |
Cell Counter | Logos Biosystems | L20001 | Used for cell counting |
Chalizon curette 5'', size 3 2.5 mm | Biomedical Research Instruments | 15-1020 | Used to transfer SV |
Chromium Next GEM single Cell 3' GEM Kit v3.1 | Chromium | PN-1000141 | Generates single cell 3' gene expression libraries |
Clear nail polish | Fisher Scientific | NC1849418 | Used for sealing SV mount |
Corning Falcon Standard Tissue Culture Dishes, 24 well | Corning | 08-772B | Culture dish used to hold specimen during dissection |
DAPI | Invitrogen | D1306, RRID: AB_2629482 | Stain used for nucleus labeling |
Dounce homogenizer | Sigma-Aldrich | D8938 | Used to homogenize tissue for sNuc-seq |
Dumont #5 Forceps | Fine Science Tools | 11252-30 | General forceps for dissection |
Dumont #55 Forceps | Fine Science Tools | 11255-20 | Forceps with fine tip that makes SV manipulation easier |
Fetal Bovine Serum | ThermoFisher | 16000044 | Used for steps of sNuc-Seq |
Glue stick | Fisher Scientific | NC0691392 | Used for mounting SV |
GS-IB4 Antibody | Molecular Probes | I21411, RRID: AB-2314662 | Antibody used for capillary labeling |
KCNJ10-ZsGreen Mice | n/a | n/a | Transgenic mouse that expresses KCNJ10-ZsGreen, partiularly in the intermediate cells of the SV. |
MgCl2 | ThermoFisher | AM9530G | Used for steps of sNuc-Seq |
Mounting reagent | ThermoFisher | #S36940 | Mounting reagent for SV |
Multiwell 24 well plate | Corning | #353047 | Plate used for immunostaining |
NaCl | ThermoFisher | AAJ216183 | Used for steps of sNuc-Seq |
Nonidet P40 | Sigma-Aldrich | 9-16-45-9 | Used for steps of sNuc-Seq |
Nuclease free water | ThermoFisher | 4387936 | Used for steps of sNuc-Seq |
Orbital shaker | Silent Shake | SYC-2102A | Used for steps of immunostaining |
PBS | ThermoFisher | J61196.AP | Used for steps of immunostaining and dissection |
RNA Later | Invitrogen | AM7021 | Used for preservation of SV for sNuc-Seq |
Scizzors | Fine Science Tools | 14058-09 | Used for splitting mouse skull |
Tris-HCl | Sigma-Aldrich | 15506017 | Used for steps of sNuc-Seq |
Trypan blue stain | Gibco | 15250061 | Used for cell counting |
Tween20 | ThermoFisher | AAJ20605AP | Used for steps of sNuc-Seq |
Zeiss STEMI SV 11 Apo stereomicroscope | Zeiss | n/a | Microscope used for dissections |
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