PMID- 26164455 OWN - NLM STAT- MEDLINE DCOM- 20160420 LR - 20150713 IS - 1473-558X (Electronic) IS - 0959-4965 (Linking) VI - 26 IP - 12 DP - 2015 Aug 19 TI - Auditory stimulation modulates CXCL12/CXCR4 expression in postnatal development of the newborn rat cochlea. PG - 681-7 LID - 10.1097/WNR.0000000000000408 [doi] AB - Sensorineural hearing loss is one of the most common sensory deficits. Recently, inner-ear stem cell therapy has been proposed for auditory afferent rehabilitation. CXCR4 is the primary physiologic receptor for CXC chemokine ligand 12 (CXCL12) and the CXCL12-CXCR4 pathway has been implicated in the process of migration, differentiation, and maturation of vertebrate neural stem cells. In this study, we examined changes in the auditory brainstem response and CXCL12/CXCR4 expression in newborn rat cochleae under different acoustic environments by quantitative real-time PCR, western blot, enzyme-linked immunosorbent assay, immunohistochemistry, and immunofluorescence analyses. Rats were divided randomly into three groups: the augmented acoustic environment (AAE) group, the auditory deprivation (AD) group, and the control group. Auditory brainstem response thresholds were markedly increased in the AAE group and in the AD group. Compared with postnatal day 1, the expression of CXCL12/CXCR4 mRNA and protein under normal acoustic conditions was increased on postnatal day 14 and then decreased on postnatal day 28 in the cochlea. However, on postnatal day 28, CXCL12/CXCR4 expression, as well as its spatiotemporal distribution as detected by immunohistochemistry and immunofluorescence assays, was augmented by AAE treatment and inhibited by AD treatment. Therefore, our results confirmed that auditory stimulation influenced the spatiotemporal expression of CXCL12/CXCR4 in newborn rat cochlea, which might help to unravel the role of the CXCL12-CXCR4 pathway in the synaptic contacts and hearing function establishment in rat cochlea development. CI - Copyright (c) 2015 Wolters Kluwer Health, Inc. All rights reserved. FAU - Zhang, Wen AU - Zhang W AD - aDepartment of Surgery, The Second Affiliated Hospital, Xi'an Jiaotong University bDepartment of Otolaryngology, The Fourth People's Hospital of Shaanxi Province cDepartment of Otolaryngology, Xijing Hospital, Fourth Military Medical University dDepartment of Otolaryngology, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi, People's Republic of China. FAU - Zhang, Fangjun AU - Zhang F FAU - Han, Yu AU - Han Y FAU - Liu, Hui AU - Liu H FAU - Wang, Ye AU - Wang Y FAU - Yue, Bo AU - Yue B FAU - Chen, Jun AU - Chen J FAU - Chen, Yang AU - Chen Y FAU - Gao, Ya AU - Gao Y LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - England TA - Neuroreport JT - Neuroreport JID - 9100935 RN - 0 (CXCL12 protein, rat) RN - 0 (Chemokine CXCL12) RN - 0 (Cxcr4 protein, rat) RN - 0 (Receptors, CXCR4) SB - IM MH - Acoustic Stimulation/*methods MH - Animals MH - Animals, Newborn MH - Chemokine CXCL12/*biosynthesis/genetics MH - Cochlea/*growth & development/*metabolism MH - *Gene Expression Regulation, Developmental MH - Rats MH - Rats, Sprague-Dawley MH - Receptors, CXCR4/*biosynthesis/genetics EDAT- 2015/07/15 06:00 MHDA- 2016/04/21 06:00 CRDT- 2015/07/13 06:00 PHST- 2015/07/13 06:00 [entrez] PHST- 2015/07/15 06:00 [pubmed] PHST- 2016/04/21 06:00 [medline] AID - 00001756-201508020-00004 [pii] AID - 10.1097/WNR.0000000000000408 [doi] PST - ppublish SO - Neuroreport. 2015 Aug 19;26(12):681-7. doi: 10.1097/WNR.0000000000000408.