Cornwall Gail A, von Horsten H Henning, Swartz Douglas, Johnson Seethal, Chau Kim, Whelly Sandra
Department of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center, 3601 4th Street, Lubbock, TX 79430, USA.
Asian J Androl. 2007 Jul;9(4):500-7. doi: 10.1111/j.1745-7262.2007.00309.x.
The epididymal lumen represents a unique extracellular environment because of the active sperm maturation process that takes place within its confines. Although much focus has been placed on the interaction of epididymal secretory proteins with spermatozoa in the lumen, very little is known regarding how the complex epididymal milieu as a whole is maintained, including mechanisms to prevent or control proteins that may not stay in their native folded state following secretion. Because some misfolded proteins can form cytotoxic aggregate structures known as amyloid, it is likely that control/surveillance mechanisms exist within the epididymis to protect against this process and allow sperm maturation to occur. To study protein aggregation and to identify extracellular quality control mechanisms in the epididymis, we used the cystatin family of cysteine protease inhibitors, including cystatin-related epididymal spermatogenic and cystatin C as molecular models because both proteins have inherent properties to aggregate and form amyloid. In this chapter, we present a brief summary of protein aggregation by the amyloid pathway based on what is known from other organ systems and describe quality control mechanisms that exist intracellularly to control protein misfolding and aggregation. We then present a summary of our studies of cystatin-related epididymal spermatogenic (CRES) oligomerization within the epididymal lumen, including studies suggesting that transglutaminase cross-linking may be one mechanism of extracellular quality control within the epididymis.
附睾管腔代表着一种独特的细胞外环境,这是由于在其范围内发生的活跃精子成熟过程。尽管人们十分关注附睾分泌蛋白与管腔内精子的相互作用,但对于整个复杂的附睾微环境是如何维持的,包括防止或控制那些分泌后可能无法保持天然折叠状态的蛋白质的机制,却知之甚少。由于一些错误折叠的蛋白质会形成被称为淀粉样蛋白的细胞毒性聚集结构,因此附睾内很可能存在控制/监测机制来防止这一过程,并使精子成熟得以发生。为了研究蛋白质聚集并确定附睾中的细胞外质量控制机制,我们使用了半胱氨酸蛋白酶抑制剂的胱抑素家族,包括与胱抑素相关的附睾生精蛋白和胱抑素C作为分子模型,因为这两种蛋白质都具有聚集并形成淀粉样蛋白的固有特性。在本章中,我们基于从其他器官系统了解到的情况,简要总结了淀粉样蛋白途径导致的蛋白质聚集,并描述了细胞内存在的控制蛋白质错误折叠和聚集的质量控制机制。然后,我们总结了我们对附睾管腔内与胱抑素相关的附睾生精蛋白(CRES)寡聚化的研究,包括表明转谷氨酰胺酶交联可能是附睾内细胞外质量控制的一种机制的研究。