scholarly journals Membrane hyperpolarization during human sperm capacitation

2014 ◽  
Vol 20 (7) ◽  
pp. 619-629 ◽  
Author(s):  
I. López-González ◽  
P. Torres-Rodríguez ◽  
O. Sánchez-Carranza ◽  
A. Solís-López ◽  
C.M. Santi ◽  
...  
2020 ◽  
Vol 22 (1) ◽  
pp. 93
Author(s):  
Arturo Matamoros-Volante ◽  
Valeria Castillo-Viveros ◽  
Paulina Torres-Rodríguez ◽  
Marcela B. Treviño ◽  
Claudia L. Treviño

Plasma membrane (PM) hyperpolarization, increased intracellular pH (pHi), and changes in intracellular calcium concentration ([Ca2+]i) are physiological events that occur during human sperm capacitation. These parameters are potential predictors of successful outcomes for men undergoing artificial reproduction techniques (ARTs), but methods currently available for their determination pose various technical challenges and limitations. Here, we developed a novel strategy employing time-lapse flow cytometry (TLFC) to determine capacitation-related membrane potential (Em) and pHi changes, and progesterone-induced [Ca2+]i increases. Our results show that TLFC is a robust method to measure absolute Em and pHi values and to qualitatively evaluate [Ca2+]i changes. To support the usefulness of our methodology, we used sperm from two types of normozoospermic donors: known paternity (subjects with self-reported paternity) and no-known paternity (subjects without self-reported paternity and no known fertility problems). We found relevant differences between them. The incidences of membrane hyperpolarization, pHi alkalinization, and increased [Ca2+]i were consistently high among known paternity samples (100%, 100%, and 86%, respectively), while they varied widely among no-known paternity samples (44%, 17%, and 45%, respectively). Our results indicate that TLFC is a powerful tool to analyze key physiological parameters of human sperm, which pending clinical validation, could potentially be employed as fertility predictors.


2021 ◽  
Vol 35 (6) ◽  
Author(s):  
Paula A. Balestrini ◽  
Claudia Sanchez‐Cardenas ◽  
Guillermina M. Luque ◽  
Carolina Baro Graf ◽  
Jessica M. Sierra ◽  
...  

2009 ◽  
Vol 46 (10) ◽  
pp. 1420-1427 ◽  
Author(s):  
Eve de Lamirande ◽  
Geneviève Lamothe ◽  
Michèle Villemure

2001 ◽  
Vol 45 (1) ◽  
pp. 12-20 ◽  
Author(s):  
TOMOMI AOYAMA ◽  
YASUHIKO OZAKI ◽  
KAORU SUZUMORI ◽  
YASUHIKO OZAKI ◽  
MITOSHI KUNIMATSU ◽  
...  

2018 ◽  
Vol 234 (4) ◽  
pp. 5276-5288 ◽  
Author(s):  
Nicolás Gastón Brukman ◽  
Sol Yanel Nuñez ◽  
Lis del Carmen Puga Molina ◽  
Mariano Gabriel Buffone ◽  
Alberto Darszon ◽  
...  

Andrology ◽  
2019 ◽  
Vol 8 (2) ◽  
pp. 442-449 ◽  
Author(s):  
L. Mayorga ◽  
K. Altamirano ◽  
E. Zanni Ruiz ◽  
M. Pavarotti

2019 ◽  
Vol 25 (10) ◽  
pp. 587-600 ◽  
Author(s):  
Héctor Zapata-Carmona ◽  
Lina Barón ◽  
Lidia M Zuñiga ◽  
Emilce Silvina Díaz ◽  
Milene Kong ◽  
...  

Abstract One of the first events of mammalian sperm capacitation is the activation of the soluble adenyl cyclase/cAMP/protein kinase A (SACY/cAMP/PKA) pathway. Here, we evaluated whether the increase in PKA activity at the onset of human sperm capacitation is responsible for the activation of the sperm proteasome and whether this activation is required for capacitation progress. Viable human sperm were incubated with inhibitors of the SACY/cAMP/PKA pathway. The chymotrypsin-like activity of the sperm proteasome was evaluated using a fluorogenic substrate. Sperm capacitation status was evaluated using the chlortetracycline assay and tyrosine phosphorylation. To determine whether proteasomal subunits were phosphorylated by PKA, the proteasome was immunoprecipitated and tested on a western blot using an antibody against phosphorylated PKA substrates. Immunofluorescence microscopy analysis and co-immunoprecipitation (IPP) were used to investigate an association between the catalytic subunit alpha of PKA (PKA-Cα) and the proteasome. The chymotrypsin-like activity of the sperm proteasome significantly increased after 5 min of capacitation (P < 0.001) and remained high for the remaining incubation time. Treatment with H89, KT5720 or KH7 significantly decreased the chymotrypsin-like activity of the proteasome (P < 0.001). IPP experiments indicated that PKA inhibition significantly modified phosphorylation of proteasome subunits. In addition, PKA-Cα colocalized with the proteasome in the equatorial segment and in the connecting piece, and co-immunoprecipitated with the proteasome. This is the first demonstration of sperm proteasome activity being directly regulated by SACY/PKA-Cα. This novel discovery extends our current knowledge of sperm physiology and may be used to manage sperm capacitation during assisted reproductive technology procedures.


2012 ◽  
Vol 87 (Suppl_1) ◽  
pp. 448-448
Author(s):  
Patricio J. Morales ◽  
Kely Ordenes ◽  
Lidia Zuñiga ◽  
Emilce S. Diaz

2012 ◽  
Vol 87 (Suppl_1) ◽  
pp. 425-425
Author(s):  
Lidia M. Zuñiga ◽  
Kely Ordenes ◽  
Emilce S. Diaz ◽  
Patricio Morales

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