Troyanovskaya M, Wackym P A
Department of Otolaryngology, Mount Sinai School of Medicine, New York, NY, USA.
Hear Res. 1998 Dec;126(1-2):201-9. doi: 10.1016/s0378-5955(98)00163-4.
P2X2 receptors are ligand-gated ion channels that are activated by extracellular ATP. To characterize the expression of P2X2 purinoceptor in the adult rat vestibular periphery, reverse transcription-polymerase chain reaction (RT-PCR) was used. No transcript for P2X2 receptor was found in the vestibular primary afferent neurons (Scarpa's ganglia); however, partial cDNAs encoding four splice variants of the P2X2 receptor were isolated from vestibular end-organs. In all four cDNAs, the deletions were of different lengths but started at the same position on the P2X2 gene (Val-370 codon) located toward the intracellular carboxyl terminus. One of these receptor isoforms was identical in sequence to the recently published P2X2(b) receptor (Simon et al., 1997, Mol. Pharmacol. 52, 237-248) (also known as P2X2-2, in the nomenclature of Brändle et al., 1997, FEBS Lett. 404, 294-298). The remaining three novel splice variants of the P2X2 receptor were designated P2X2(e), P2X2(f) and P2X2(g) (GenBank accession numbers AF028603, AF028604 and AF028605, respectively). The functional significance of these three splice variants remains to be determined. Pituitary and cerebellum were used as survey tissues and only the P2X2(b) receptor cDNA was found.
P2X2受体是由细胞外ATP激活的配体门控离子通道。为了表征成年大鼠前庭外周中P2X2嘌呤受体的表达,采用了逆转录-聚合酶链反应(RT-PCR)。在前庭初级传入神经元(斯卡帕神经节)中未发现P2X2受体的转录本;然而,从前庭终末器官中分离出了编码P2X2受体四种剪接变体的部分cDNA。在所有四个cDNA中,缺失的长度不同,但都始于位于细胞内羧基末端的P2X2基因上的相同位置(Val-370密码子)。其中一种受体亚型的序列与最近发表的P2X2(b)受体相同(Simon等人,1997年,《分子药理学》52卷,237-248页)(在Brändle等人1997年的命名法中也称为P2X2-2,《欧洲生物化学学会联合会快报》404卷,294-298页)。P2X2受体的其余三种新的剪接变体被命名为P2X2(e)、P2X2(f)和P2X2(g)(GenBank登录号分别为AF028603、AF028604和AF028605)。这三种剪接变体的功能意义仍有待确定。垂体和小脑用作检测组织,仅发现了P2X2(b)受体cDNA。