4.6 Article

Host defense functions of the epididymal amyloid matrix

期刊

MOLECULAR HUMAN REPRODUCTION
卷 28, 期 12, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/molehr/gaac038

关键词

amyloid; epididymis; reproductive tract; host defense; cystatin; CRES; bacterial ghost; E; coli; epididymitis

资金

  1. TTUHSC
  2. Newby Family

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This study reveals the role of the epididymal amyloid matrix in host defense, showing that CRES amyloids and epididymal amyloids have potent antimicrobial activity against bacteria causing epididymal infections. The amyloids use various defense mechanisms and elicit strain-specific host defense responses.
The epididymal lumen is an immunologically distinct environment. It maintains tolerance for the naturally antigenic spermatozoa to allow their maturation into functional cells while simultaneously defending against pathogens that can ascend the male tract and cause infertility. We previously demonstrated that a nonpathological amyloid matrix that includes several cystatin-related epididymal spermatogenic (CRES) subgroup family members is distributed throughout the mouse epididymal lumen but its function was unknown. Here, we reveal a role for the epididymal amyloid matrix in host defense and demonstrate that the CRES amyloids and CD-1 mouse epididymal amyloid matrix exhibit potent antimicrobial activity against bacterial strains that commonly cause epididymal infections in men. We show the CRES and epididymal amyloids use several defense mechanisms including bacterial trapping, disruption of bacterial membranes and promotion of unique bacterial ghost-like structures. Remarkably, these antimicrobial actions varied depending on the bacterial strain indicating CRES amyloids and the epididymal amyloids elicit strain-specific host defense responses. We also demonstrate that the CRES monomer and immature assemblies of the epididymal amyloid transitioned into advanced structures in the presence of bacteria, suggesting their amyloid-forming/shape-shifting properties allows for a rapid reaction to a pathogen and provides an inherent plasticity in their host defense response. Together, our studies reveal new mechanistic insight into how the male reproductive tract defends against pathogens. Future studies using a mouse model for human epididymitis are needed to establish the epididymal amyloid responses to pathogens in vivo. Broadly, our studies provide an example of why nature has maintained the amyloid fold throughout evolution.

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