Research Service-151, Loma Linda Veterans Affairs Medical Center, Loma Linda, California 92357, USA. O’
Int J Neurosci. 2012 Dec;122(12):757-66. doi: 10.3109/00207454.2012.721828. Epub 2012 Oct 16.
ABSTRACT 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.
为了应对压力,螺旋神经节神经元可能会重塑细胞内的 DNA 修复蛋白库。通过确定正常条件下、噪声应激(105dB/4 小时)后以及随后的 DNA 修复佐剂羧基烷基酯(CAE;160mg/kg/28 天)治疗后三种经典 DNA 切除修复蛋白(XPA、CSA 和 XPC)在神经元中的细胞内位置,验证了这一假说。在正常条件下,至少有一种修复蛋白富集于三种细胞内隔室中。这些细胞内隔室被指定为核、胞质和核周。噪声应激后,每种修复蛋白都在细胞质中聚集。CAE 治疗后,每个细胞内隔室都富含三种 DNA 修复蛋白。将噪声应激与 CAE 治疗相结合,导致每个细胞内隔室中至少有两种修复蛋白的富集。联合结果表明,为了应对噪声应激和/或耳保护治疗,螺旋神经节神经元可能会选择性地重塑细胞内分区的 DNA 修复蛋白。