新生大鼠损伤和缺氧后内耳巢蛋白相关基因的表达

J. Gross, H. Olze, B. Mazurek
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引用次数: 1

摘要

我们利用新生大鼠血管纹(SV)、Corti器官(OC)和modiolus (MOD)的器官型培养,分析了预备损伤和缺氧后细胞骨架、髓鞘和神经生长因子相关基因的差异表达水平和反应。24小时内,神经丝Nefl、Nefm、微管相关蛋白Mapt、Map1a、Map2和髓鞘碱性蛋白Mbp的转录本mRNA水平在MOD和OC区域协调下降。MOD区域细胞死亡率的增加与Nes(编码中间丝巢蛋白的转录物)、神经生长因子受体Ngfr、生长相关蛋白43 Gap43和浦肯野细胞蛋白Pcp4的表达增加有关。相关分析显示,Nes的表达与凋亡和坏死细胞死亡相关基因(caspase Casp3、calpain Capn1、Capn2、Capns1)、谷氨酸通路(谷氨酸受体NMDA相关蛋白1 Grina、胶质高亲和谷氨酸转运蛋白Slc1a3)、细胞骨架基因(Nefm、Map2、Map1a、Mbp)、转录因子(缺氧诱导因子Hif-1a、jun原癌基因jun、脑表达髓细胞瘤病B-myc、HES家族bHLH转录因子1 HES -1, forkhead-box D3 Foxd3)和神经生长因子(Ngfr, Gap43和Pcp4)。Nes集群的独特反应和组成使我们得出结论,细胞死亡相关基因和再生相关基因的表达是协调的,在MOD和OC/SV区域之间是不同的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression of nestin-associated genes in the inner ear of newborn rats following injury and hypoxia
We used organotypic cultures of the stria vascularis (SV), the organ of Corti (OC) and the modiolus (MOD) of newborn rats to analyze the differential expression levels and responses of cytoskeletal, myelin- and neural growth factor-associated genes following preparatory injury and hypoxia. The transcript mRNA levels of the neurofilaments Nefl , Nefm, the microtubule-associated proteins Mapt, Map1a, Map2, and of the myelin basic protein Mbp decrease during 24 h in a coordinated way across the MOD and OC regions. The increased cell death rate in the MOD region is associated with an increased expression of Nes, the transcript encoding the intermediate filament nestin, and of the neural growth factor receptor Ngfr, the growth-associated protein 43 Gap43 and the Purkinje cell protein Pcp4. The correlation analysis revealed close associations between Nes expression and genes involved in apoptotic and necrotic cell death (caspase Casp3, calpains Capn1, Capn2, Capns1), the glutamate pathway (glutamate receptor NMDA associated protein 1 Grina, glial high affinity glutamate transporter Slc1a3), cytoskeletal genes (Nefm, Map2, Map1a, Mbp), transcription factors (hypoxia inducible factor Hif-1a, jun proto-oncogene Jun, brain expressed myelocytomatosis B-myc, HES family bHLH transcription factor 1 Hes-1, forkhead-box D3 Foxd3) and neural growth factors ( Ngfr, Gap43 and Pcp4 ) . The unique response and the composition of the Nes cluster made us conclude that the expression of cell-death-associated genes and the regeneration-associated genes takes place in a coordinated way, and differs between the MOD and the OC/SV regions.
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