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Actin nucleator Spire 1 is a regulator of ectoplasmic specialization in the testis

机译:肌动蛋白成核剂Spire 1是睾丸胞浆专化的调节剂

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Germ cell differentiation during the epithelial cycle of spermatogenesis is accompanied by extensive remodeling at the Sertoli cell–cell and Sertoli cell–spermatid interface to accommodate the transport of preleptotene spermatocytes and developing spermatids across the blood–testis barrier (BTB) and the adluminal compartment of the seminiferous epithelium, respectively. The unique cell junction in the testis is the actin-rich ectoplasmic specialization (ES) designated basal ES at the Sertoli cell–cell interface, and the apical ES at the Sertoli–spermatid interface. Since ES dynamics (i.e., disassembly, reassembly and stabilization) are supported by actin microfilaments, which rapidly converts between their bundled and unbundled/branched configuration to confer plasticity to the ES, it is logical to speculate that actin nucleation proteins play a crucial role to ES dynamics. Herein, we reported findings that Spire 1, an actin nucleator known to polymerize actins into long stretches of linear microfilaments in cells, is an important regulator of ES dynamics. Its knockdown by RNAi in Sertoli cells cultured in vitro was found to impede the Sertoli cell tight junction (TJ)-permeability barrier through changes in the organization of F-actin across Sertoli cell cytosol. Unexpectedly, Spire 1 knockdown also perturbed microtubule (MT) organization in Sertoli cells cultured in vitro. Biochemical studies using cultured Sertoli cells and specific F-actin vs. MT polymerization assays supported the notion that a transient loss of Spire 1 by RNAi disrupted Sertoli cell actin and MT polymerization and bundling activities. These findings in vitro were reproduced in studies in vivo by RNAi using Spire 1-specific siRNA duplexes to transfect testes with Polyplus in vivo-jetPEI as a transfection medium with high transfection efficiency. Spire 1 knockdown in the testis led to gross disruption of F-actin and MT organization across the seminiferous epithelium, thereby impeding the transport of spermatids and phagosomes across the epithelium and perturbing spermatogenesis. In summary, Spire 1 is an ES regulator to support germ cell development during spermatogenesis.
机译:精子发生上皮细胞周期中的生殖细胞分化伴随着Sertoli细胞-细胞和Sertoli细胞-精子细胞界面的广泛重塑,以适应前瘦素精子细胞的运输和发育中的精子细胞穿过血睾丸屏障(BTB)和分别是生精上皮。睾丸中独特的细胞连接是在Sertoli细胞-细胞界面上称为基础ES的富含肌动蛋白的胞质特化(ES),以及在Sertoli-精子细胞界面上称为顶端的ES。由于肌动蛋白微丝支持ES动力学(即拆卸,重新组装和稳定化),而肌动蛋白微丝会在它们的成束和非成束/支化构型之间快速转换以赋予ES可塑性,因此逻辑上推测肌动蛋白成核蛋白对ES动态。在这里,我们报道了发现,Spire 1(一种肌动蛋白成核剂,已知可将肌动蛋白聚合成细胞中的长条线性微丝)是ES动态的重要调节剂。发现通过在体外培养的Sertoli细胞中通过RNAi抑制它的作用,可通过F-actin在整个Sertoli细胞胞质溶胶中的组织变化来阻止Sertoli细胞紧密连接(TJ)-渗透性屏障。出乎意料的是,Spire 1敲低还干扰了体外培养的Sertoli细胞中的微管(MT)组织。使用培养的Sertoli细胞和特定的F-肌动蛋白与MT聚合分析进行的生化研究支持以下观点:RNAi导致Spire 1的瞬时丧失会破坏Sertoli细胞的肌动蛋白以及MT聚合和捆绑活性。 RNAi使用Spire 1特异性siRNA双链体以Polyplus in-jetPEI作为转染介质以高转染效率转染睾丸,在体内研究中通过RNAi复制了这些体外研究结果。睾丸中的Spire 1敲低导致F-肌动蛋白和MT组织在整个生精上皮细胞的整体破坏,从而阻碍了精子和吞噬体在上皮细胞中的运输并扰乱了精子的生成。总之,Spire 1是在精子发生过程中支持生殖细胞发育的ES调节剂。

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