Barón L, Fara K, Zapata-Carmona H, Zuñiga L, Kong M, Signorelli J, Díaz E S, Morales P
Laboratory of Biology of Reproduction, Department of Biomedicine, Faculty of Health Sciences, University of Antofagasta, Antofagasta, Chile.
Antofagasta Institute, University of Antofagasta, Antofagasta, Chile.
Andrology. 2016 Nov;4(6):1073-1083. doi: 10.1111/andr.12234. Epub 2016 Oct 1.
In human spermatozoa, protein kinases have a role in the acrosome reaction (AR) induced by a variety of stimuli. However, there is disagreement or a lack of information regarding the role of protein kinases and phosphatases in the progesterone (P)-induced increase in intracellular calcium concentration ([Ca ] ). In addition, there are no studies regarding the role of Ser/Thr and Tyr phosphatases and there are contradictory results regarding the role of Tyr kinases in the P-induced acrosome reaction. Here, we performed a simultaneous evaluation of the involvement of protein kinases and phosphatases in the P-induced acrosome reaction and in the P-induced calcium influx. Motile spermatozoa were capacitated for 18 h and different aliquots were allocated to treated or control groups and then evaluated for their ability to undergo the acrosome reaction and to increase [Ca ] in response to P. The acrosome reaction was evaluated using Pisum sativum agglutinin (PSA)-FITC, and [Ca ] was evaluated using fura 2AM. At all of the concentrations tested, PKA inhibitors significantly reduced the percentage of the P-induced acrosome reaction (p < 0.001). However, only the highest concentrations of PKA inhibitors reduced the P-induced calcium influx; lower concentrations of PKA inhibitors did not affect it. Similar results were apparent for PKC inhibitors and for tyrosine kinase inhibitors. None of the Ser/Thr phosphatase inhibitors affected the P-induced acrosome reaction or the P-induced calcium influx, except for the PP2B inhibitors that significantly reduced the P-induced acrosome reaction without affecting calcium influx. Finally, the protein tyrosine phosphatase inhibitors significantly blocked the P-induced acrosome reaction and reduced the amplitude of the P-induced calcium transient (p < 0.001) as well as the amplitude of the plateau phase (p < 0.01). The data suggest that protein kinases and possibly PP2B have a role on the acrosome reaction at some point downstream of calcium entry and that Tyr phosphatases have a role on the acrosome reaction upstream of calcium entry.
在人类精子中,蛋白激酶在多种刺激诱导的顶体反应(AR)中发挥作用。然而,关于蛋白激酶和磷酸酶在孕酮(P)诱导的细胞内钙浓度([Ca])升高过程中的作用,存在分歧或信息不足。此外,尚无关于丝氨酸/苏氨酸磷酸酶和酪氨酸磷酸酶作用的研究,且关于酪氨酸激酶在P诱导的顶体反应中的作用存在相互矛盾的结果。在此,我们同时评估了蛋白激酶和磷酸酶在P诱导的顶体反应及P诱导的钙内流中的作用。将活动精子进行18小时的获能处理,然后将不同等分试样分配到处理组或对照组,接着评估它们发生顶体反应以及对P作出反应时增加[Ca]的能力。使用豌豆凝集素(PSA)-异硫氰酸荧光素(FITC)评估顶体反应,使用fura 2AM评估[Ca]。在所有测试浓度下,蛋白激酶A(PKA)抑制剂均显著降低P诱导的顶体反应百分比(p < 0.001)。然而,只有最高浓度的PKA抑制剂降低了P诱导的钙内流;较低浓度的PKA抑制剂未对其产生影响。蛋白激酶C(PKC)抑制剂和酪氨酸激酶抑制剂也出现了类似结果。除了能显著降低P诱导的顶体反应而不影响钙内流的蛋白磷酸酶2B(PP2B)抑制剂外,丝氨酸/苏氨酸磷酸酶抑制剂均未影响P诱导的顶体反应或P诱导的钙内流。最后,蛋白酪氨酸磷酸酶抑制剂显著阻断了P诱导的顶体反应,降低了P诱导的钙瞬变幅度(p < 0.001)以及平台期幅度(p < 0.01)。数据表明,蛋白激酶以及可能的PP2B在钙进入后的某个下游点对顶体反应起作用,而酪氨酸磷酸酶在钙进入的上游对顶体反应起作用。