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lüll Extracellular quality control in the epididymis Cornwall GA; von Horsten HH; Swartz D; Johnson S; Chau K; Whelly SAsian J Androl 2007[Jul]; 9 (4): 500-7The 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.|Amino Acid Substitution[MESH]|Amyloid/physiology/standards[MESH]|Cystatin C[MESH]|Cystatins/genetics[MESH]|Dimerization[MESH]|Epididymis/*physiology[MESH]|Humans[MESH]|Male[MESH]|Mutation[MESH]|Protein Folding[MESH]|Proteins/standards[MESH]|Quality Control[MESH]|Sperm Maturation/*physiology[MESH]|Transglutaminases/physiology[MESH] |