The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, China.
The Mary M. Wohlford Laboratory for Male Contraceptive Research, Center for Biomedical Research, Population Council, New York, New York, USA.
FASEB J. 2021 Oct;35(10):e21925. doi: 10.1096/fj.202100960R.
In mammalian testes, extensive remodeling of the microtubule (MT) and actin cytoskeletons takes place in Sertoli cells across the seminiferous epithelium to support spermatogenesis. However, the mechanism(s) involving regulatory and signaling proteins remains poorly understood. Herein, A-kinase anchoring protein 9 (AKAP9, a member of the AKAP multivalent scaffold protein family) was shown to be one of these crucial regulatory proteins in the rat testis. Earlier studies have shown that AKAP9 serves as a signaling platform by recruiting multiple signaling and regulatory proteins to create a large protein complex that binds to the Golgi and centrosome to facilitate the assembly of the MT-nucleating γ-tubulin ring complex to initiate MT polymerization. We further expanded our earlier studies based on a Sertoli cell-specific AKAP9 knockout mouse model to probe the function of AKAP9 by using the techniques of immunofluorescence analysis, RNA interference (RNAi), and biochemical assays on an in vitro primary Sertoli cell culture model, and an adjudin-based animal model. AKAP9 robustly expressed across the seminiferous epithelium in adult rat testes, colocalizing with MT-based tracks, and laid perpendicular across the seminiferous epithelium, and prominently expressed at the Sertoli-spermatid cell-cell anchoring junction (called apical ectoplasmic specialization [ES]) and at the Sertoli cell-cell interface (called basal ES, which together with tight junction [TJ] created the blood-testis barrier [BTB]) stage specifically. AKAP9 knockdown in Sertoli cells by RNAi was found to perturb the TJ-permeability barrier through disruptive changes in the distribution of BTB-associated proteins at the Sertoli cell cortical zone, mediated by a considerable loss of ability to induce both MT polymerization and actin filament bundling. A considerable decline in AKAP9 expression and a disruptive distribution of AKAP9 across the seminiferous tubules was also noted during adjudin-induced germ cell (GC) exfoliation in this animal model, illustrating AKAP9 is essential to maintain the homeostasis of cytoskeletons to maintain Sertoli and GC adhesion in the testis.
在哺乳动物的睾丸中,在生精上皮中,支持精子发生的 Sertoli 细胞中广泛发生微管 (MT) 和肌动蛋白细胞骨架的重塑。然而,涉及调节和信号蛋白的机制仍知之甚少。本文证明,激酶锚定蛋白 9 (AKAP9,AKAP 多价支架蛋白家族的成员之一) 是大鼠睾丸中这些关键调节蛋白之一。早期研究表明,AKAP9 通过招募多种信号和调节蛋白作为信号平台,形成一个大的蛋白质复合物,与高尔基体和中心体结合,促进 MT 成核 γ-微管蛋白环复合物的组装,从而启动 MT 聚合。我们进一步扩展了我们之前基于 Sertoli 细胞特异性 AKAP9 敲除小鼠模型的研究,通过在体外原代 Sertoli 细胞培养模型和基于 adjudin 的动物模型中使用免疫荧光分析、RNA 干扰 (RNAi) 和生化测定技术,来探究 AKAP9 的功能。AKAP9 在成年大鼠睾丸的生精上皮中强烈表达,与基于 MT 的轨道共定位,并垂直于生精上皮排列,在 Sertoli-精子细胞细胞锚定连接 (称为顶质外特化 [ES]) 和 Sertoli 细胞-细胞界面 (称为基底 ES,与紧密连接 [TJ] 一起形成血睾屏障 [BTB]) 阶段特别表达。通过 RNAi 在 Sertoli 细胞中敲低 AKAP9 发现,通过破坏 BTB 相关蛋白在 Sertoli 细胞皮质区的分布,扰乱 TJ 通透性屏障,这是通过丧失诱导 MT 聚合和肌动蛋白丝 bundling 的能力介导的。在这个动物模型中,在用 adjudin 诱导生精细胞 (GC) 脱落期间,还观察到 AKAP9 在生精小管中的表达显著下降和分布紊乱,表明 AKAP9 对于维持细胞骨架的动态平衡以维持睾丸中 Sertoli 和 GC 的黏附是必不可少的。