Elevated aminopeptidase N affects sperm motility and early embryo development

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Abstract

Aminopeptidase N (APN) is a naturally occurring ectopeptidase present in mammalian semen. Previous studies have demonstrated that APN adversely affects male fertility through the alteration of sperm motility. This enzyme constitutes 0.5 to 1% of the seminal plasma proteins, which can be transferred from the prostasomes to sperms by a fusion process. In the present study, we investigated the molecular mechanism of action of APN and its role in regulating sperm functions and male fertility. In this in vitro study, epididymal mouse spermatozoa were incubated in a capacitating media (pH 7) containing 20 ng/mL of recombinant mouse APN for 90 min. Our results demonstrated that the supplementation of recombinant APN in sperm culture medium significantly increased APN activity, and subsequently altered motility, hyperactivated motility, rapid and medium swimming speeds, viability, and the acrosome reaction of mouse spermatozoa. These effects were potentially caused by increased toxicity in the spermatozoa. Further, altered APN activity in sperm culture medium affected early embryonic development. Interestingly, the effect of elevated APN activity in sperm culture medium was independent of protein tyrosine phosphorylation and protein kinase A activity. On the basis of these results, we concluded that APN plays a significant role in the regulation of several sperm functions and early embryonic development. In addition, increased APN activity could potentially lead to several adverse consequences related to male fertility.

Figures

  • Fig 1. Localization of APN in spermatozoa and the effect of recombinant APN (20 ng/mL) on APN level and its enzymatic activity in mouse spermatozoa. (A) Localization of APN (green). (B) Location of nucleus (Hoechst 33258, blue). (C) Location of the acrosome (lectin PNA, red). (D) Merged location of the nucleus, acrosome, and APN. Images were obtained using the Nikon TS-1000 microscope and NIS-Elements imaging software (Nikon, Japan). Bar = 20 μm. (E) Quantification of APN in spermatozoa. (F) Representative image of western blot showing the band (~100 kDa) corresponding to APN in the spermatozoa (P = 0.234). (G) Enzymatic activity of APN in the control and treated groups (P = 0.00001). Data represent the mean ± SEM of three replicates. *P < 0.05, calculated using two-tailed Student’s t-test.
  • Fig 2. Effects of addition of recombinant APN (20 ng/mL) on motility, hyperactive motility, viability, LDH, and intracellular ROS levels in mice spermatozoa. (A) Sperm motility (%) (P = 0.00001). (B) Hyperactive motility (HYP%) (P = 0.003). Data represent the mean ± SEM of four replicates. (C) The percentage of rapid- (P = 0.00001), medium- (P = 0.001), and slow-speed (P = 0.053) spermatozoa (D) The percentage of viable spermatozoa (P = 0.002). (E) LDH levels (P = 0.045). (F) Intracellular ROS levels (P = 0.142). Data represent the mean ± SEM of three replicates. *P < 0.05, calculated using two-tailed Student’s t-test.
  • Fig 3. Effect of recombinant APN (20 ng/mL) on the capacitation status of mouse spermatozoa. Different patterns of spermatozoa, such as (A) acrosome-reacted (AR pattern), capacitated (B pattern), non capacitated (F pattern), and dead (D pattern), observed after combined Hoechst 33258/chlortetracycline fluorescence staining. (B) Difference in AR pattern spermatozoa (P = 0.006). (C) Difference in B pattern spermatozoa (P = 0.100). (D) Difference in F pattern spermatozoa (P = 0.123). Data represent the mean ± SEM of three replicates. *P < 0.05, calculated using two-tailed Student’s t-test.
  • Fig 4. Effect of addition of recombinant APN (20 ng/mL) on protein tyrosine phosphorylation and PKA activity in mouse spermatozoa. (A) Densities of tyrosine phosphorylated proteins (~90 and 30 kDa) in the control and treated groups (P = 0.179 and 0.215, respectively). (B) Representative image of the western blot for tyrosine phosphorylated proteins. (C) Densities of PKA substrates (~55 and 34 kDa) in the control and treated groups (P = 0.353 and 0.342, respectively). (D) Representative image of the western blot for phospho-PKA substrates. Data represent the mean ± SEM of three replicates. *P < 0.05, calculated using two-tailed Student’s t-test.
  • Fig 5. Effect of recombinant APN on fertilization and embryonic development. (A) Blastocyst quality in the control and APN-treated groups (Bar = 50 μM). Red, blue, and yellow arrows indicate grade 1, 2, and 3 blastocysts, respectively. (B) Difference in cleavage rate between the control and treated groups (P = 0.568). (C) Blastocyst formation rate in the control and treated groups (P = 0.008). Data represent the mean ± SEM of three replicates. *P < 0.05, calculated using two-tailed Student’s t-test. (D) Effect of APN on mouse spermatozoa and its hypothetical mechanisms of action. High APN activity induces toxicity in spermatozoa and subsequently decreases sperm motility, viability, and acrosome reaction. Ultimately, the affected spermatozoa display pathological conditions induced by dysregulation of early embryonic development.
  • Fig 6. Illustration of the APN-regulated proteins, cellular functions, and diseases analyzed using the Pathway Studio program.

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APA

Khatun, A., Rahman, M. S., Ryu, D. Y., Kwon, W. S., & Pang, M. G. (2017). Elevated aminopeptidase N affects sperm motility and early embryo development. PLoS ONE, 12(8). https://doi.org/10.1371/journal.pone.0184294

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