Li Linxi, Tang Elizabeth I, Chen Haiqi, Lian Qingquan, Ge Renshan, Silvestrini Bruno, Cheng C Yan
Mary M. Wohlford Laboratory for Male Contraceptive Research, Center for Biomedical Research.
Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, China.
Endocrinology. 2017 Dec 1;158(12):4300-4316. doi: 10.1210/en.2017-00660.
The mechanism that regulates sperm release at spermiation is unknown. Herein, we used an animal model wherein rats were treated with adjudin, 1-(2,4-dichlorobenzyl)-1H-indazole-3-carbohydrazide, via oral gavage to induce premature release of elongating/elongated spermatids, followed by round spermatids and spermatocytes. Spermatid release mimicking spermiation occurred within 6 to 12 hours following adjudin treatment and, by 96 hours, virtually all tubules were devoid of elongating/elongated spermatids. Using this model, we tracked the organization of F-actin and microtubules (MTs) by immunofluorescence microscopy, and the association of actin or MT regulatory proteins that either promote or demolish cytoskeletal integrity through changes in the organization of actin microfilaments or MTs by coimmunoprecipitation. Adjudin treatment induced an increase in the association of (1) epidermal growth factor receptor pathway substrate 8 (an actin barbed-end capping and bundling protein) or formin 1 (an actin nucleator) with actin and (2) end-binding protein 1 (an MT stabilizing protein) with MT shortly after adjudin exposure (at 6 hours), in an attempt to maintain spermatid adhesion to the Sertoli cell at the apical ectoplasmic specialization (ES). However, this was followed by a considerable decline of their steady-state protein levels, replacing with an increase in association of (1) actin-related protein 3 (a branched actin nucleator that converts actin filaments into a branched/unbundled network) with actin and (2) MT affinity-regulating kinase 4 (an MT destabilizing protein kinase) with MTs by 12 hours after adjudin treatment. These latter changes thus promoted actin and MT disorganization, leading to apical ES disruption and the release of elongating/elongated spermatids, mimicking spermiation. In summary, spermiation is a cytoskeletal-dependent event, involving regulatory proteins that modify cytoskeletal organization.
精子释放期调节精子释放的机制尚不清楚。在此,我们使用了一种动物模型,通过口服灌胃给予大鼠阿地津(1-(2,4-二氯苄基)-1H-吲唑-3-碳酰肼),以诱导延长型/延长的精子细胞过早释放,随后是圆形精子细胞和精母细胞。阿地津处理后6至12小时内发生了模拟精子释放期的精子细胞释放,到96小时时,几乎所有的曲细精管都没有延长型/延长的精子细胞。利用该模型,我们通过免疫荧光显微镜追踪F-肌动蛋白和微管(MTs)的组织情况,并通过免疫共沉淀法追踪肌动蛋白或MT调节蛋白的关联,这些蛋白通过改变肌动蛋白微丝或MTs的组织来促进或破坏细胞骨架的完整性。阿地津处理后不久(6小时),诱导了以下关联增加:(1) 表皮生长因子受体途径底物8(一种肌动蛋白尖端封端和捆绑蛋白)或formin 1(一种肌动蛋白成核剂)与肌动蛋白,以及(2) 末端结合蛋白1(一种MT稳定蛋白)与MT,试图在顶端外质特化(ES)处维持精子细胞与支持细胞的黏附。然而,随后它们的稳态蛋白水平大幅下降,取而代之的是,阿地津处理12小时后,(1) 肌动蛋白相关蛋白3(一种将肌动蛋白丝转化为分支/非捆绑网络的分支肌动蛋白成核剂)与肌动蛋白,以及(2) MT亲和力调节激酶4(一种MT不稳定蛋白激酶)与MTs的关联增加。因此,这些后期变化促进了肌动蛋白和MT的解聚,导致顶端ES破坏和延长型/延长的精子细胞释放,模拟精子释放期。总之,精子释放期是一个依赖细胞骨架的事件,涉及修饰细胞骨架组织的调节蛋白。