蝾螈肢体再生胚母细胞存在和不存在情况下背根神经节体外转录反应的表征。

Antony Athippozhy, Jeffrey Lehrberg, James R Monaghan, David M Gardiner, S Randal Voss
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引用次数: 14

摘要

在蝾螈肢体再生过程中,神经提供的信号诱导了大量增殖细胞的形成,这些细胞被称为胚基。为了更好地理解这些信号,我们开发了一个胚基-背根神经节(DRG)共培养模型系统,以验证神经在响应胚基提供的信号时差异表达基因的假设。从蝾螈(Ambystoma mexicanum)中分离近端和远端神经干DRG,培养5天,进行微阵列分析。与新分离的DRG相比,1541个Affymetrix探针组被鉴定为差异表达,并且已知许多预测的基因在哺乳动物DRG观察到的损伤和神经发育反应中起作用。然后,我们将5天的DRG外植体与胚母细胞共培养或不共培养再培养5天。在第10天,我们鉴定了27个基因,这些基因在培养的DRG中的表达受到胚母细胞存在或不存在的显著影响。总的来说,我们的研究建立了drg -胚泡体外培养系统,并为未来研究轴突再生、神经胚泡信号传导和肢体再生的神经调节确定了候选基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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