Departamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, México.
Biol Reprod. 2012 Oct 18;87(4):92. doi: 10.1095/biolreprod.112.100255. Print 2012 Oct.
Spermatogenic cell differentiation involves changes in the concentration of cytoplasmic Ca(2+) ([Ca(2+)]i); however, very few studies exist on [Ca(2+)]i dynamics in these cells. Other tissues display Ca(2+) oscillations involving multicellular functional arrangements. These phenomena have been studied in acute slice preparations that preserve tissue architecture and intercellular communications. Here we report the implementation of intracellular Ca(2+) imaging in a sliced seminiferous tubule (SST) preparation to visualize [Ca(2+)]i changes of living germ cells in situ within the SST preparation. Ca(2+) imaging revealed that a subpopulation of male germ cells display spontaneous [Ca(2+)]i fluctuations resulting from Ca(2+) entry possibly throughout Ca(V)3 channels. These [Ca(2+)]i fluctuation patterns are also present in single acutely dissociated germ cells, but they differ from those recorded from germ cells in the SST preparation. Often, spontaneous Ca(2+) fluctuations of spermatogenic cells in the SST occur synchronously, so that clusters of cells can display Ca(2+) oscillations for at least 10 min. Synchronous Ca(2+) oscillations could be mediated by intercellular communication via gap junctions, although intercellular bridges could also be involved. We also observed an increase in [Ca(2+)]i after testosterone application, suggesting the presence of functional Sertoli cells in the SST. In summary, we believe that the SST preparation is suitable to explore the physiology of spermatogenic cells in their natural environment, within the seminiferous tubules, in particular Ca(2+) signaling phenomena, functional cell-cell communication, and multicellular functional arrangements.
精子发生细胞的分化涉及细胞质 Ca(2+) 浓度 ([Ca(2+)]i) 的变化;然而,关于这些细胞中 [Ca(2+)]i 动力学的研究很少。其他组织显示涉及多细胞功能排列的 Ca(2+) 振荡。这些现象已在急性切片制备中进行了研究,这些制备方法保留了组织结构和细胞间通讯。在这里,我们报告了在切片生精小管 (SST) 制备中实施细胞内 Ca(2+) 成像的情况,以可视化 SST 制备中活精子细胞内 [Ca(2+)]i 的变化。Ca(2+) 成像显示,一部分雄性生殖细胞显示自发的 [Ca(2+)]i 波动,这可能是由于 Ca(V)3 通道的 Ca(2+) 进入引起的。这些 [Ca(2+)]i 波动模式也存在于急性分离的单个生殖细胞中,但与从 SST 制备中记录的生殖细胞记录的模式不同。通常,SST 中精子发生细胞的自发 Ca(2+) 波动会同步发生,因此至少可以持续 10 分钟。同步 Ca(2+) 振荡可以通过缝隙连接的细胞间通讯来介导,尽管细胞间桥也可能参与其中。我们还观察到睾酮应用后 [Ca(2+)]i 的增加,这表明 SST 中存在功能性支持细胞。总之,我们认为 SST 制备适合在其天然环境中生精小管内探索精子发生细胞的生理学,特别是 Ca(2+) 信号转导现象、功能性细胞-细胞通讯和多细胞功能排列。