Department of Physiology, Faculty of Medical and Health Sciences, The University of Auckland, Aukland, New Zealand.
J Neurosci Res. 2010 Sep;88(12):2598-609. doi: 10.1002/jnr.22421.
Adenosine signalling has an important role in cochlear protection from oxidative stress. In most tissues, intracellular adenosine kinase (ADK) is the primary route of adenosine metabolism and the key regulator of intracellular and extracellular adenosine levels. The present study provides the first evidence for ADK distribution in the adult and developing rat cochlea. In the adult cochlea, ADK was localized to the nuclear or perinuclear region of spiral ganglion neurons, lateral wall tissues, and epithelial cells lining scala media. In the developing cochlea, ADK was strongly expressed in multiple cell types at birth and reached its peak level of expression at postnatal day 21 (P21). Ontogenetic changes in ADK expression were evident in the spiral ganglion, organ of Corti, and stria vascularis. In the spiral ganglion, ADK showed a shift from predominantly satellite cell immunolabelling at P1 to neuronal expression from P14 onward. In contrast to the role of ADK in various aspects of cochlear development, the ADK contribution to the cochlear response to noise stress was less obvious. Transcript and protein levels of ADK were unaltered in the cochlea exposed to broadband noise (90-110 dBSPL, 24 hr), and the selective inhibition of ADK in the cochlea with ABT-702 failed to restore hearing thresholds after exposure to traumatic noise. This study indicates that ADK is involved in purine salvage pathways for nucleotide synthesis in the adult cochlea, but its role in the regulation of adenosine signalling under physiological and pathological conditions has yet to be established.
腺苷信号在耳蜗免受氧化应激的保护中具有重要作用。在大多数组织中,细胞内腺苷激酶(ADK)是腺苷代谢的主要途径,也是细胞内和细胞外腺苷水平的关键调节剂。本研究首次提供了 ADK 在成年和发育中的大鼠耳蜗中的分布证据。在成年耳蜗中,ADK 定位于螺旋神经节神经元的核或核周区域、侧壁组织和衬里中阶的上皮细胞。在发育中的耳蜗中,ADK 在出生时强烈表达于多种细胞类型,并在出生后第 21 天(P21)达到表达高峰。ADK 表达的个体发育变化在螺旋神经节、柯蒂氏器和血管纹中显而易见。在螺旋神经节中,ADK 从 P1 时主要定位于卫星细胞免疫标记转变为 P14 以后的神经元表达。与 ADK 在耳蜗发育各个方面的作用相反,ADK 对耳蜗对噪声应激的反应的贡献不太明显。暴露于宽带噪声(90-110dBSPL,24 小时)后,耳蜗中的 ADK 转录本和蛋白水平没有改变,并且用 ABT-702 选择性抑制耳蜗中的 ADK 也未能在暴露于创伤性噪声后恢复听力阈值。本研究表明,ADK 参与成年耳蜗中核苷酸合成的嘌呤补救途径,但它在生理和病理条件下调节腺苷信号的作用尚未确定。