Herr Deron R, Grillet Nicolas, Schwander Martin, Rivera Richard, Müller Ulrich, Chun Jerold
Department of Molecular Biology, Helen L. Dorris Institute for Neurological and Psychiatric Disorders, La Jolla, California 92037, USA.
J Neurosci. 2007 Feb 7;27(6):1474-8. doi: 10.1523/JNEUROSCI.4245-06.2007.
Hearing requires the transduction of vibrational forces by specialized epithelial cells in the cochlea known as hair cells. The human ear contains a finite number of terminally differentiated hair cells that, once lost by noise-induced damage or toxic insult, can never be regenerated. We report here that sphingosine 1-phosphate (S1P) signaling, mainly via activation of its cognate receptor S1P2, is required for the maintenance of vestibular and cochlear hair cells in vivo. Two S1P receptors, S1P2 and S1P3, were found to be expressed in the cochlea by reverse transcription-PCR and in situ hybridization. Mice that are null for both these receptors uniformly display progressive cochlear and vestibular defects with hair cell loss, resulting in complete deafness by 4 weeks of age and, with complete penetrance, balance defects of increasing severity. This study reveals the previously unknown role of S1P signaling in the maintenance of cochlear and vestibular integrity and suggests a means for therapeutic intervention in degenerative hearing loss.
听力需要耳蜗中称为毛细胞的特殊上皮细胞将振动力进行转导。人类耳朵含有有限数量的终末分化毛细胞,一旦因噪声损伤或毒性损伤而丢失,就永远无法再生。我们在此报告,鞘氨醇-1-磷酸(S1P)信号传导,主要通过激活其同源受体S1P2,是体内维持前庭和耳蜗毛细胞所必需的。通过逆转录-聚合酶链反应和原位杂交发现,两种S1P受体S1P2和S1P3在耳蜗中表达。这两种受体均缺失的小鼠均表现出进行性耳蜗和前庭缺陷以及毛细胞丢失,到4周龄时导致完全失聪,并且具有完全的外显率,平衡缺陷的严重程度不断增加。这项研究揭示了S1P信号传导在维持耳蜗和前庭完整性方面以前未知的作用,并提出了一种对退行性听力损失进行治疗干预的方法。