Background: Spermatogenesis is regulated by a complex network of intercellular communication processes. Extracellular vesicles (EVs) are one of the important mediators in intercellular communication. Previous reports have demonstrated the involvement of EVs from the epididymis and prostate in sperm maturation and function. However, the presence of EVs in the testis and their potential involvement in spermatogenesis has not been explored. Here, we have established a testis dissociation protocol that allows the isolation and characterization of testicular EVs.

Results: We show that testicular EVs are specifically and efficiently taken up by somatic cells and germ cells, including the spermatozoa in the interstitial space and the seminiferous tubule compartments. We profiled the proteome of testicular EVs and probed the cell types that release them, revealing the potential contributions from the Leydig cells and testicular macrophages. Moreover, we sequenced the small RNA cargoes of testicular EVs and identified sets of small non-coding RNAs that were overlooked in the testis transcriptome. Selected miRNA candidates in testicular EVs were found in sperm RNA payload and demonstrated specific resistance towards ribonuclease A independent of the vesicle membrane. Small molecule inhibition of EV secretion perturbed spermatogenesis via inter-compartmental communication.

Conclusions: Together, our study provides a valuable resource on the repertoire of cargoes carried by testicular EVs and uncovers a physiological function of testicular EVs in inter-compartmental communication associated to spermatogenesis.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966158PMC
http://dx.doi.org/10.1186/s12915-022-01268-5DOI Listing

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Article Synopsis
  • Key proteins from epididymal extracellular vesicles (EVs) help mature sperm cells by improving their centrosomal functions and development potential.
  • The study focused on the presence and role of galectin-3-binding protein (LGALS3BP) in EVs, finding it increases in sperm during epididymal transit and affects fertilization ability.
  • Inhibiting LGALS3BP led to decreased fertilization rates and slower cell cycles, highlighting its significance and potential for improving fertility treatments.
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