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Here, we present an immunocytochemical and electron microscopical protocol that enables qualitative and quantitative characterization of the interaction of the primary spiral ganglion neurons and other cell types within ultrathin polymer films.
The spiral ganglion (SG) cells prepared from the inner ear of postnatal rats represent one of the key cell culture models in hearing research. Numerous projects in hearing research aim at improving nerve-electrode-interactions by inhibiting the formation of connective tissue following cochlear implant insertion, i.e., by coating the carrier material with ultrathin polymer films for selective cell attachment. Here, we established scanning electron microscopy (SEM) and immunocytochemical (ICC) staining to enable the characterization of the interactions of fibroblasts, glial cells, and spiral ganglion neurons (SGN) growing on polymers, i.e., poly(N,N-dimethylacrylamide) (PDMAA), poly(2-ethyloxazoline) (PEtOx), and poly([2-methacryloyloxy)ethyl]trimethylammoniumchloride) (PMTA). For this purpose the primary cells dissociated from the SG of postnatal rats were cultivated for 48 h on the polymer films. ICC was used to demonstrate the preferences of cell adhesion on the polymer coatings. It could be shown that glial cells and SGN mainly adhered on PMTA monolayers forming long processes, but not on PDMAA and PEtOx films. Also, SEM imaging showed that only PMTA enabled SG neuron survival and neurite outgrowth. In conclusion, the ability of the SGN to survive and to form neurites was associated with glial cell adhesion on different coatings.
Numerous projects in hearing research aim at improving nerve-electrode-interactions by inhibiting the formation of connective tissue following cochlear implant insertion by either application of drugs like dexamethasone1,2,3,4, coating the carrier material with ultrathin polymer films5,6,7,8, or nano structuring of the carrier materials for selective cell attachment9,
Neonatal Spraque-Dawley rats (P3-5, n = 18 per experiment, n = 5 independent experiments) were used for SG dissection in accordance with the institutional guidelines for animal welfare of Hannover Medical School following the standards described by the German "Law on protecting animals" (Tierschutzgesetz).
1. Dissection of the Cochlear SG from Neonatal Rats 13,14
The aim of establishing the ICC protocol was the differentiation of the cell types accompanying the adhesion and neurite outgrowth of the SG neurons. As shown in Figure 1A-H, the method detected not only the expression of the neurofilaments in SGN, but also vimentin in both fibroblasts and glial cells on the polymer films (Figure 1A, C, E, G). Double staining with anti-vimentin a.......
This study represents for the first time the differential interactions of SGN, glial cells, and fibroblasts on varying polymer films. Staining of the specific intermediary filaments and the neurotrophic growth factor receptor enabled not only a strong distinction between the cell types and their morphology following adhesion, but also the quantitative determination of the interesting cell types. Hereby, as described in Hadler et al.7, the growth of fibroblasts was clearly scaled down on t.......
The support of S. Zwittian and G. Preiss, Institute of Cell Biology, Hannover Medical School for was greatly appreciated. This study was funded by the Deutsche Forschungsgemeinschaft (SFB 599, subproject D2).
....Name | Company | Catalog Number | Comments |
Animals | |||
Sprague-Dawley rats | Charles River, Sulzfeld, Germany | Inbreeding strain, ordered and provided by the Laboratory Animal Sciences, Medical School Hannover, Germany | |
Laboratory equipment | |||
Transmission light microscope Leica MZ-6 | Leica, Germany | Preparation of the cochlear structures | |
Inverse microscope: Keyence BZ 9000 Biorevo | Keyence International, Mechelen, Belgium | Fluorescence microscopy | |
SEM 505 | Philips, NL | Scanning electron microscopy | |
CPD 030 | Balzers Union, Balzers FL | Critical point drying | |
Polaron E5400 | Watford Hertfordshire, England | High resolution sputter coater | |
Laboratory tools | |||
Standard Pattern Forceps, curved/12 cm | Fine Science Tools, Heidelberg, Germany | 11001-12 | Dissection of the spiral ganglia from postnatal rats |
Adson-Brown Forceps, Shark Teeth | Fine Science Tools, Heidelberg, Germany | 11627-12 | Dissection of the spiral ganglia from postnatal rats |
Forceps Dumont #3c, straight/11 cm | Fine Science Tools, Heidelberg, Germany | 11231-20 | Dissection of the spiral ganglia from postnatal rats |
Forceps Dumont Medical #5, straight | Fine Science Tools, Heidelberg, Germany | 11255-20 | Dissection of the spiral ganglia from postnatal rats |
Scissor, pointed-pointed, straight/11 cm | Wirtschaftsgenossenschaft deutscher Tierärzte (WDT) eG, Garbsen, Germany | 27040 | Dissection of the spiral ganglia from postnatal rats |
Plastic and glass material | |||
48well-microtiter plate | Nunc/thermo Scientific | 150787 | |
Coverslips Menzel-Gläser 24 x 60 mm | VWR International GmbH, Darmstadt, Germany | 631-0973 | |
Buffers, enzymes, proteins, chemicals, cell culture supplements | |||
Acetone | Mallinckrodt Baker R.V., Griesheim, Germany | 9002-02 | |
Argon | Linde Gas, Pullach, Germany | Argon 5.0 | |
Bovine serum albumine | Sigma-Aldrich, St.Louis, USA | A3294 | Lyophilized powder, initial fraction by heat shock, fraction V. |
DNase I | Roche, Basel, Switzerland | 11284932001 | |
Fetal bovine serum (FBS) | Biochrom, Berlin, Germany | S0415 | |
Glucose 40 % concentrate | Our lab is receiving glucose by the hospital pharmacy. | ||
Glutardialdehyde | Polysciences, Warrington, PA, USA | 01909-10 | |
Hank’s balanced salt solution (HBSS) | Invitrogen/Fisher Scientific, Waltham, MA, USA | 14170-070 | Ca2+/ Mg2+-free |
HEPES | Invitrogen/Fisher Scientific, Waltham, MA, USA | 15630-056 | 1 M |
Insulin from bovine pancreas | Sigma-Aldrich, St.Louis, USA | I0516 | |
Leit-C | Plano, Wetzlar, Germany | G3300 | fluid carbon in xylol |
N2-Supplement | Invitrogen/Fisher Scientific, Waltham, MA, USA | 17502-048 | 100x |
Natural Mouse Laminin | Invitrogen/Fisher Scientific, Waltham, MA, USA | 23017-015 | |
Panserin 401 neuro medium | PAN Biotech, Aidenbach, Germany | P04-710401 | Neuro medium for cultivation neuronal cells |
Phosphate buffered saline (PBS) tablets | Invitrogen/Fisher Scientific, Waltham, MA, USA | 18912-014 | Ca2+/ Mg2+-free |
Penicillin G Sodium salt | Sigma-Aldrich, St.Louis, USA | PENNA-10MU | |
Poly-DL-Ornithin hydrobromid | Sigma-Aldrich, St.Louis, USA | P8638 | |
Prolong anti-fade Gold with DAPI | Invitrogen/Fisher Scientific, Waltham, MA, USA | P36941 | DAPI containing mounting gel |
Sodium cacodylate | Sigma-Aldrich, St.Louis, USA | C4945-10G | |
Triton-X 100 | Sigma-Aldrich, St.Louis, USA | T8787 | |
Trypan Blue | Sigma-Aldrich, St.Louis, USA | T 8154 | |
Trypsin | Biochrom, Berlin, Germany | L2123 | 1:250 in PBS, Ca2+/ Mg2+-free |
Primary antibodies | |||
Neurofilament 200kD, mouse, monoclonal | Novocastra, Newcastle upon Tyne, UK | NCL-NF200 | |
p75, rabbit, polyclonal | Abcam, Cambridge, UK | 38335 | |
Vimentin clone V9, mouse, monoclonal | Dako GmbH, Jena, Germany | M0725 | |
Vimentin, chicken, polyclonal | Abcam, Cambridge, UK | ab24525 | |
Secondary antibodies | |||
Goat anti-chicken, conjugated with Texas Red | Santa Cruz Biotech., Dallas, TX, USA | sc2994 | |
Goat anti-mouse, conjugated with New dylight 488 | Jackson-Immunoresearch Laboratories Inc., West Grove, PA, USA | 115-485-008 | |
Goat anti-rabbit, conjugated with Alexa Fluor 594 | Jackson-Immunoresearch Laboratories Inc., West Grove, PA, USA | 111-515-144 |
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