Influence of BMI, Cigarette Smoking and Cryopreservation on Tyrosine Phosphorylation during Sperm Capacitation

Author:

Ortiz-Vallecillo Ana1ORCID,Santamaría-López Esther2,García-Ruiz Diego1ORCID,Martín-Lozano David3,Candenas Luz3,Pinto Francisco M.3ORCID,Fernández-Sánchez Manuel245ORCID,González-Ravina Cristina156

Affiliation:

1. IVIRMA Global Research Alliance, IVI Foundation, Instituto de Investigación Sanitaria La Fe, Avenida Fernando Abril Martorell, 106-Torre A, Planta 1ª, 46026 Valencia, Spain

2. VIDA RECOLETAS Seville, Calle Américo Vespucio, 19, 41092 Seville, Spain

3. Instituto de Investigaciones Químicas, CSIC, Calle Américo Vespucio, 49, 41092 Seville, Spain

4. Departamento de Cirugía, Universidad de Sevilla, Avenida Sánchez Pizjuán, S/N, 41009 Seville, Spain

5. Departamento de Biología Molecular e Ingeniería Bioquímica, Universidad Pablo de Olavide, Carretera de Utrera, 1, 41013 Seville, Spain

6. IVI-RMA Global Headquarters, Calle Américo Vespucio, 5, 41092 Seville, Spain

Abstract

Capacitation involves tyrosine phosphorylation (TP) as a key marker. Lifestyle-related factors, such as obesity and smoking, are recognized for their adverse effects on semen quality and male fertility, yet the underlying mechanisms, including their potential impact on TP, remain unclear. Moreover, the effect of sperm cryopreservation on TP at the human sperm population level is unexplored. Flow cytometry analysis of global TP was performed on pre-capacitated, post-capacitated and 1- and 3-hours’ incubated fresh and frozen–thawed samples from sperm donors (n = 40). Neither being overweight nor smoking (or both) significantly affected the percentage of sperm showing TP. However, elevated BMI and smoking intensity correlated with heightened basal TP levels (r = 0.226, p = 0.003) and heightened increase in TP after 3 h of incubation (r = 0.185, p = 0.017), respectively. Cryopreservation resulted in increased global TP levels after capacitation but not immediately after thawing. Nonetheless, most donors’ thawed samples showed increased TP levels before and after capacitation as well as after incubation. Additionally, phosphorylation patterns in fresh and frozen–thawed samples were similar, indicating consistent sample response to capacitation stimuli despite differences in TP levels. Overall, this study sheds light on the potential impacts of lifestyle factors and cryopreservation on the dynamics of global TP levels during capacitation.

Funder

Centro para el Desarrollo Tecnológico Industrial

Ministry of Science, Innovation and Universities, Government of Spain

Publisher

MDPI AG

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