Dickerson Ian M, Bussey-Gaborski Rhiannon, Holt Joseph C, Jordan Paivi M, Luebke Anne E
Deptartment of Neuroscience, University of Rochester Medical Center, Rochester New York.
Deptartment of Biomedical Engineering, University of Rochester Medical Center, Rochester, New York.
Physiol Rep. 2016 Jul;4(14). doi: 10.14814/phy2.12869.
In adult animals, the neuropeptide calcitonin gene-related peptide (CGRP) is contained in cochlear efferent fibers projecting out to the cochlea, and contributes to increased suprathreshold sound-evoked activity in the adult auditory nerve. Similarly, CGRP applied to the lateral-line organ (hair cell organ) increases afferent nerve activity in adult frogs (post-metamorphic day 30), yet this increase is developmentally delayed from post-metamorphic day 4-30. In this study, we discovered that there was also a developmental delay in increased suprathreshold sound-evoked activity auditory nerve between juvenile and adult mice similar to what had been observed previously in frog. Moreover, juvenile mice with a targeted deletion of the αCGRP gene [CGRP null (-/-)] did not show a similar developmental increase in nerve activity, suggesting CGRP signaling is involved. This developmental delay is not due to a delay in CGRP expression, but instead is due to a delay in receptor formation. We observed that the increase in sound-evoked nerve activity is correlated with increased formation of cochlear CGRP receptors, which require three complexed proteins (CLR, RAMP1, RCP) to be functional. CGRP receptor formation in the cochlea was incomplete at 1 month of age (juvenile), but complete by 3 months (adult), which corresponded to the onset of suprathreshold enhancement of sound-evoked activity in wild-type animals. Taken together, these data support a model for cochlear function that is enhanced by maturation of CGRP receptor complexes.
在成年动物中,神经肽降钙素基因相关肽(CGRP)存在于投射至耳蜗的耳蜗传出纤维中,并有助于增强成年听神经中超阈值声音诱发的活动。同样,将CGRP应用于侧线器官(毛细胞器官)可增加成年青蛙(变态后第30天)的传入神经活动,但这种增加在变态后第4 - 30天出现发育延迟。在本研究中,我们发现幼年和成年小鼠之间超阈值声音诱发的听神经活动增加也存在发育延迟,这与之前在青蛙中观察到的情况类似。此外,靶向缺失αCGRP基因的幼年小鼠[CGRP基因敲除(-/-)]并未表现出类似的神经活动发育性增加,提示CGRP信号传导参与其中。这种发育延迟并非由于CGRP表达延迟,而是由于受体形成延迟。我们观察到声音诱发的神经活动增加与耳蜗CGRP受体形成增加相关,而CGRP受体需要三种复合蛋白(CLR、RAMP1、RCP)才能发挥功能。耳蜗中的CGRP受体形成在1月龄(幼年)时不完整,但在3月龄(成年)时完整,这与野生型动物中超阈值声音诱发活动增强的开始时间相对应。综上所述,这些数据支持了一种耳蜗功能模型,即CGRP受体复合物的成熟可增强耳蜗功能。