TY - JOUR
T1 - Dynamic compartmentalization of DNA repair proteins within spiral ganglion neurons in response to noise stress
AU - Guthrie, O'Neil W.
N1 - Funding Information:
This work was supported by a CDA-2 (C7600-W) Award from the Rehabilitation Research and Development Service of the Office of Research and Development United States Department of Veterans Affairs. The Loma Linda Veterans Affairs Medical Center provided facilities for conducting the experiments.
PY - 2012/12
Y1 - 2012/12
N2 - In response to stress, spiral ganglion neurons may remodel intracellular pools of DNA repair proteins. This hypothesis was addressed by determining the intracellular location of three classic DNA excision repair proteins (XPA, CSA, and XPC) within the neurons under normal conditions, one day after noise stress (105 dB/4 hr) and following DNA repair adjuvant therapy with carboxy alkyl esters (CAEs; 160 mg/kg/28 days). Under normal conditions, three intracellular compartments were enriched with at least one repair protein. These intracellular compartments were designated nuclear, cytoplasmic, and perinuclear. After the noise stress each repair protein aggregated in the cytoplasm. After CAE therapy each intracellular compartment was enriched with the three DNA repair proteins. Combining noise stress with CAE therapy resulted in the enrichment of at least two repair proteins in each intracellular compartment. The combined results suggest that in response to noise stress and/or otoprotective therapy, spiral ganglion neurons may selectively remodel compartmentalized DNA repair proteins.
AB - In response to stress, spiral ganglion neurons may remodel intracellular pools of DNA repair proteins. This hypothesis was addressed by determining the intracellular location of three classic DNA excision repair proteins (XPA, CSA, and XPC) within the neurons under normal conditions, one day after noise stress (105 dB/4 hr) and following DNA repair adjuvant therapy with carboxy alkyl esters (CAEs; 160 mg/kg/28 days). Under normal conditions, three intracellular compartments were enriched with at least one repair protein. These intracellular compartments were designated nuclear, cytoplasmic, and perinuclear. After the noise stress each repair protein aggregated in the cytoplasm. After CAE therapy each intracellular compartment was enriched with the three DNA repair proteins. Combining noise stress with CAE therapy resulted in the enrichment of at least two repair proteins in each intracellular compartment. The combined results suggest that in response to noise stress and/or otoprotective therapy, spiral ganglion neurons may selectively remodel compartmentalized DNA repair proteins.
KW - auditory sensory neurons
KW - cochlear stress
KW - noise induced hearing loss
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U2 - 10.3109/00207454.2012.721828
DO - 10.3109/00207454.2012.721828
M3 - Article
C2 - 22900489
AN - SCOPUS:84869770468
SN - 0020-7454
VL - 122
SP - 757
EP - 766
JO - International Journal of Neuroscience
JF - International Journal of Neuroscience
IS - 12
ER -