Donoso María Verónica, Norambuena Andrés, Navarrete Camilo, Poblete Inés, Velasco Alfredo, Huidobro-Toro Juan Pablo
Laboratorio de Nucleótidos, Departamento de Fisiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Biol Reprod. 2014 Feb 6;90(2):23. doi: 10.1095/biolreprod.113.109660. Print 2014 Feb.
To assess the role of the P2X1 receptors (P2X1R) in the longitudinal and circular layers of the human vas deferens, ex vivo-isolated strips or rings were prepared from tissue biopsies to record isometric contractions. To ascertain its membrane distribution, tissue extracts were analyzed by immunoblotting following sucrose gradient ultracentrifugation. ATP, alpha,beta-methylene ATP, or electrical field stimulation elicited robust contractions of the longitudinal layer but not of the circular layer which demonstrated inconsistent responses. Alpha,beta-methylene ATP generated stronger and more robust contractions than ATP. In parallel, prostatic segments of the rat vas deferens were examined. The motor responses in both species were not sustained but decayed within the first minute, showing desensitization to additional applications. Cross-desensitization was established between alpha,beta-methylene ATP or ATP-evoked contractions and electrical field stimulation-induced contractions. Full recovery of the desensitized motor responses required more than 30 min and showed a similar pattern in human and rat tissues. Immunoblot analysis of the human vas deferens extracts revealed a P2X1R oligomer of approximately 200 kDa under nonreducing conditions, whereas dithiothreitol-treated extracts showed a single band of approximately 70 kDa. The P2X1R was identified in ultracentrifugation fractions containing 15%-29% sucrose; the receptor localized in the same fractions as flotillin-1, indicating that it regionalized into smooth muscle lipid rafts. In conclusion, ATP plays a key role in human vas deferens contractile responses of the longitudinal smooth muscle layer, an effect mediated through P2X1Rs.
为评估P2X1受体(P2X1R)在人类输精管纵行肌层和环行肌层中的作用,从组织活检中制备离体分离的条带或环,以记录等长收缩。为确定其膜分布,在蔗糖梯度超速离心后通过免疫印迹分析组织提取物。ATP、α,β-亚甲基ATP或电场刺激可引起纵行肌层强烈收缩,但环行肌层无此反应,环行肌层反应不一致。α,β-亚甲基ATP比ATP产生更强且更持久的收缩。同时,对大鼠输精管的前列腺段进行了检查。两个物种的运动反应均不持久,在第一分钟内就衰减,显示对额外刺激脱敏。在α,β-亚甲基ATP或ATP诱发的收缩与电场刺激诱导的收缩之间建立了交叉脱敏。脱敏后的运动反应完全恢复需要超过30分钟,并且在人类和大鼠组织中表现出相似的模式。对人类输精管提取物的免疫印迹分析显示,在非还原条件下有一个约200 kDa的P2X1R寡聚体,而经二硫苏糖醇处理的提取物显示出一条约70 kDa的单带。在含有15%-29%蔗糖的超速离心级分中鉴定出P2X1R;该受体与浮舰蛋白-1定位于相同级分,表明它定位于平滑肌脂筏中。总之,ATP在人类输精管纵行平滑肌层的收缩反应中起关键作用,这一作用通过P2X1R介导。