CC BY-NC-ND 4.0 · Laryngorhinootologie 2018; 97(S 02): S252
DOI: 10.1055/s-0038-1640585
Abstracts
Otologie: Otology
Georg Thieme Verlag KG Stuttgart · New York

Analysis of the human perilymph proteome with focus on the presence of BDNF-regulated proteins

H Schmitt
1  MHH/Department of Otorhinolaryngology, Hannover
,
A Warnecke
1  MHH/Department of Otorhinolaryngology, Hannover
,
I De Vries
1  MHH/Department of Otorhinolaryngology, Hannover
,
T Lenarz
1  MHH/Department of Otorhinolaryngology, Hannover
,
S Alvi
2  University of Kansas School of Medicine/Department of Otolaryngology, Kansas City, USA
,
N Prenzler
1  MHH/Department of Otorhinolaryngology, Hannover
,
M Durisin
1  MHH/Department of Otorhinolaryngology, Hannover
,
H Staecker
2  University of Kansas School of Medicine/Department of Otolaryngology, Kansas City, USA
› Author Affiliations
This work was supported by the DFG Cluster of Excellence EXC 1077/1 "Hearing4all".
Further Information
Dr. rer. nat. Heike Schmitt
MHH/Department of Otorhinolaryngology,
Carl-Neuberg-Str.1, 30625,
Hannover

Publication History

Publication Date:
18 April 2018 (online)

 
 

    Introduction:

    Due to the fact of limited histological access to the cochlea, most causes of inner ear disorders are unknown or poorly understood and also diagnostic methods are limited. The development of a mass spectrometric proteome analysis of human perilymph (PL) opens a new perspective for the evaluation of PL specific biomarkers.

    Methods:

    Human PL samples were obtained intraoperatively during CI-surgeries. The identification of PL proteins was performed by Shot-gun proteomics (Orbitrap Massenspektrometer, Thermo Fisher Scientific) and quantified using Max Quant Software. The identified proteins were analyzed by IPA (Ingenuity pathway analysis) and the results obtained were correlated to the patients' prae- und postoperative audiological data.

    Results:

    41 perilymph samples were analyzed by mass spectrometry revealing in 878 different proteins in total. Ingenuity pathway analysis of PL proteins delineated putative intracellular pathways connected to BDNF (brain-derived neurotrophic factor) signaling in the inner ear. A correlation of protein quantification to the patients' audiological data is currently in analysis.

    Conclusions:

    In-depth proteome analysis of human PL opens a window for understanding molecular pathology of the inner ear. The neurotrophin BDNF has been implicated with the health of the auditory nerve and the growth of neurons at all. The method is feasible to develop new therapeutic strategies to improve inner ear health which could increase cochlear implant performance.


    #

    No conflict of interest has been declared by the author(s).

    Dr. rer. nat. Heike Schmitt
    MHH/Department of Otorhinolaryngology,
    Carl-Neuberg-Str.1, 30625,
    Hannover