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Detection of thromboxane A(2) receptor mRNA in rabbit nodose ganglion neurons.

机译:兔结节神经节神经元中血栓烷A(2)受体mRNA的检测。

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摘要

Thromboxane A(2) (TXA(2)) is an arachidonic acid metabolite that is released during tissue trauma and elicits platelet aggregation and vascular smooth muscle contraction. Previous research has shown that TXA(2) stimulates pulmonary and cardiac vagal afferent neurons. Therefore, we hypothesized that the presence of the TXA(2) receptor (TP) in vagal neurons would allow for stimulation or modulation of these neurons by TXA(2). To test this hypothesis, single cell RT-PCR was employed using neurons obtained from primary cell cultures of nodose ganglia excised from adult rabbits. Since the sequence for the rabbit TP gene was unknown, a portion of the rabbit TP cDNA was first amplified, cloned, and sequenced. Primer sets for TP were then designed based on this sequence and used in conjunction with a neuronal marker, medium weight neurofilament (NFM), in multiplex RT-PCR reactions. Ninety-three cells were isolated from culture and RT-PCR was carried out on individual cells. Using an aliquot from the initial RT-PCR reaction, a second round of PCR was then employed in which the NFM and TP primer sets were split up into separate reactions. Twenty-three of the 82 cells that were positive for NFM were also positive for TP. Therefore, we conclude that the presence of TP mRNA in a subset of cultured nodose ganglion neurons allows for the possibility that TXA(2) may directly stimulate or modulate vagal afferent neurons.
机译:血栓烷A(2)(TXA(2))是一种花生四烯酸代谢产物,在组织创伤期间释放,并引起血小板聚集和血管平滑肌收缩。先前的研究表明,TXA(2)刺激肺和心脏迷走神经传入神经元。因此,我们假设迷走神经元中TXA(2)受体(TP)的存在将允许TXA(2)刺激或调节这些神经元。为了检验该假设,使用单细胞RT-PCR,使用从成年兔切除的结节神经节的原代细胞培养物中获得的神经元。由于兔子TP基因的序列未知,因此首先扩增,克隆和测序了兔子TP cDNA的一部分。然后根据该序列设计用于TP的引物组,并与神经元标志物中等重量的神经丝(NFM)结合使用,进行多重RT-PCR反应。从培养物中分离出93个细胞,并对单个细胞进行RT-PCR。然后使用来自最初的RT-PCR反应的等分试样,进行第二轮PCR,其中NFM和TP引物对被拆分为单独的反应。 NFM阳性的82个细胞中有23个也TP阳性。因此,我们得出结论,在培养的结节神经节神经元的子集中存在TP mRNA,使得TXA(2)可以直接刺激或调节迷走神经传入神经元。

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