首页> 外文期刊>Regeneration >Characterization of in vitro transcriptional responses of dorsal root ganglia cultured in the presence and absence of blastema cells from regenerating salamander limbs
【24h】

Characterization of in vitro transcriptional responses of dorsal root ganglia cultured in the presence and absence of blastema cells from regenerating salamander limbs

机译:在存在和不存在再生from肢胚细胞的情况下培养的背根神经节体外转录反应的表征

获取原文
           

摘要

AbstractDuring salamander limb regeneration, nerves provide signals that induce the formation of a mass of proliferative cells called the blastema. To better understand these signals, we developed a blastema−dorsal root ganglia (DRG) co-culture model system to test the hypothesis that nerves differentially express genes in response to cues provided by the blastema. DRG with proximal and distal nerve trunks were isolated from axolotls (Ambystoma mexicanum), cultured for 5 days, and subjected to microarray analysis. Relative to freshly isolated DRG, 1541 Affymetrix probe sets were identified as differentially expressed and many of the predicted genes are known to function in injury and neurodevelopmental responses observed for mammalian DRG. We then cultured 5-day DRG explants for an additional 5 days with or without co-cultured blastema cells. On day 10, we identified 27 genes whose expression in cultured DRG was significantly affected by the presence or absence of blastema cells. Overall, our study established a DRG−blastema in vitro culture system and identified candidate genes for future investigations of axon regrowth, nerve−blastema signaling, and neural regulation of limb regeneration.
机译:摘要在sal肢再生期间,神经提供信号来诱导大量增殖细胞的形成,这种细胞称为胚泡。为了更好地理解这些信号,我们开发了胚盘-背根神经节(DRG)共培养模型系统,以检验神经元对胚盘提供的提示反应而差异表达基因的假说。从a(Ambystoma mexicanum)中分离出具有近端和远端神经干的DRG,培养5天,并进行微阵列分析。相对于新鲜分离的DRG,1541 Affymetrix探针集被鉴定为差异表达,并且已知许多预测的基因在观察到的哺乳动物DRG的损伤和神经发育反应中起作用。然后,在有或没有共培养胚泡细胞的情况下,我们将5天DRG外植体再培养5天。在第10天,我们鉴定了27个基因,它们在培养的DRG中的表达受胚细胞的存在与否显着影响。总体而言,我们的研究建立了DRG-blastema体外培养系统,并确定了候选基因,用于未来轴突再生,神经-blastema信号传导和肢体再生的神经调节研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号