Mass spectrometry reveals distinct proteomic profiles in high- and low-quality stallion spermatozoa

Author:

Griffin Róisín A1,Swegen Aleona12,Baker Mark1,Aitken Robert John1,Skerrett-Byrne David A1,Silva Rodriguez Antonio3,Martín-Cano Francisco E4,Nixon Brett15,Peña Fernando J4,Delehedde Maryse6,Sergeant Nicolas67,Gibb Zamira1

Affiliation:

1. 1Priority Research Centre for Reproductive Science, University of Newcastle, New South Wales, Australia

2. 2Nuffield Department of Women’s and Reproductive Health, University of Oxford, Oxford, UK

3. 3Facility of Innovation and Analysis in Animal Source Foodstuffs, University of Extremadura, Cáceres, Spain

4. 4Laboratory of Equine Reproduction and Equine Spermatology, Veterinary Teaching Hospital, University of Extremadura, Cáceres, Spain

5. 5Pregnancy and Reproduction Program, Hunter Medical Research Institute, New South Wales, Australia

6. 6SPQI – 4BioDx-Breeding Section, Lille, France

7. 7INSERM UMRS1172, CHU-Lille, LilNCog Research Center, University of Lille, Lille, France

Abstract

The horse breeding industry relies upon optimal stallion fertility. Conventional sperm assessments provide limited information regarding ejaculate quality and are not individually predictive of fertilizing potential. The aim of this study was to harness mass spectrometry to compare the proteomic profiles of high- and low-quality stallion spermatozoa, with the ultimate goal of identifying fertility biomarker candidates. Extended stallion semen (n = 12) was fractionated using Percoll density gradients to isolate low-quality and high-quality sperm populations. Motility and morphological assessments were carried out, and proteomic analyses was conducted using UHPLC-MS/MS. High-quality spermatozoa recorded higher total (95.2 ± 0.52% vs 70.6 ± 4.20%; P ≤ 0.001) and progressive motilities (43.4 ± 3.42% vs 27.3 ± 4.32%; P ≤ 0.05), and a higher proportion of morphologically normal cells (50.2 ± 4.34% vs 38.8 ± 2.72%; P ≤ 0.05). In total, 1069 proteins were quantified by UHPLC-MS/MS, of which 22 proteins were significantly more abundant in the high-quality sperm population (P ≤ 0.05). A-kinase anchor protein 4 (AKAP4) and Hexokinase 1 (HK1) were considered possible biomarker candidates and their differential expression was confirmed by immunoblot. Protein expression was significantly correlated with total (AKAP4 R2 = 0.38, P ≤ 0.01; HK1 R2 = 0.46, P ≤ 0.001) and progressive motilities (AKAP4 R 2 = 0.51, P ≤ 0.001; HK1 R2 = 0.55, P ≤ 0.01), percentage rapid (AKAP4 R2 = 0.29, P ≤ 0.05; HK1 R2 = 0.58, P ≤ 0.001), straight-line velocity (HK1 R2 = 0.50, P ≤ 0.01) and straightness (HK1 R2 = 0.40, P ≤ 0.01). Furthermore, AKAP4 was highly susceptible to adduction by 4-hydroxynonenal (4HNE), which resulted in a global reduction in the phosphorylation profiles following capacitation. In conclusion, the proteomic profiles of high- and low-quality stallion spermatozoa differ substantially, and proteins such as AKAP4 and HK1 could serve as biomarkers of ejaculate quality.

Publisher

Bioscientifica

Subject

Cell Biology,Obstetrics and Gynecology,Endocrinology,Embryology,Reproductive Medicine

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