Department of Urology, Daping Hospital, The Third Military Medical University, Chongqing, China.
BMB Rep. 2011 Aug;44(8):541-6. doi: 10.5483/bmbrep.2011.44.8.541.
It is generally accepted that spermatozoa capacitation is associated with protein kinase A-mediated tyrosine phosphorylation. In our previous study, we identified the fibrous sheath CABYR binding protein (FSCB), which was phosphorylated by PKA. However, the phosphorylation status of FSCB protein during spermatozoa capacitation should be further investigated. To this aim, in this study, we found that phosphorylation of this 270-kDa protein occurred as early as 1 min after mouse spermatozoa capacitation, which increased over time and remained stable after 60 min. Immunoprecipitation assays demonstrated that the tyrosine and Ser/Thr phosphorylation of FSCB occurred during spermatozoa capacitation. The extent of phosphorylation and was closely associated with the PKA activity and spermatozoa motility characteristics. FSCB phosphorylation could be induced by PKA agonist DB-cAMP, but was blocked by PKA antagonist H-89.Therefore, FSCB contributes to spermatozoa capacitation in a tyrosine-phosphorylated format, which may help in further elucidating the molecular mechanism of spermatozoa capacitation.
普遍认为,精子获能与蛋白激酶 A 介导的酪氨酸磷酸化有关。在我们之前的研究中,我们鉴定了纤维鞘 CABYR 结合蛋白(FSCB),它可被 PKA 磷酸化。然而,FSCB 蛋白在精子获能过程中的磷酸化状态仍需进一步研究。为此,本研究发现,该 270 kDa 蛋白的磷酸化早在小鼠精子获能 1 分钟后就发生,且随着时间的推移而增加,并在 60 分钟后保持稳定。免疫沉淀实验表明,FSCB 的酪氨酸和丝氨酸/苏氨酸磷酸化发生在精子获能过程中。磷酸化的程度与 PKA 活性和精子运动特性密切相关。PKA 激动剂 DB-cAMP 可诱导 FSCB 磷酸化,但 PKA 拮抗剂 H-89 可阻断其磷酸化。因此,FSCB 以酪氨酸磷酸化的形式参与精子获能,这可能有助于进一步阐明精子获能的分子机制。