Cytoplasmic extrusion and the switch from creatine kinase B to M isoform are completed by the commencement of epididymal transport in human and stallion spermatozoa.
Abstract: Although in several species there is a relationship between epididymal sperm transport and fertility, in human in vitro fertilization (IVF), spermatozoa recovered from the caput epididymidis or even the rete testis are fertile. We studied two objective markers of sperm maturity in the sperm of men and stallions: creatine kinase (CK) concentrations, which are a measure of cytoplasmic retention in immature spermatozoa, and the ratio of CK-M and CK-B isoforms (% CK-M/[CK-M + CK-B]), which is proportional to the incidence of mature sperm. The CK markers and the fertilizing function are closely related: Immature sperm with cytoplasmic retention do not bind to the zona, because during cytoplasmic extrusion, the sperm plasma membrane is also remodeled. We examined whether changes in sperm CK values are still ongoing during epididymal transport, or if cellular maturation is completed prior to the arrival of sperm in the caput epididymidis. The incidences of mature sperm in human caput and corpus epididymidis (studied in six men with obstructive azoospermia of various pathogeneses) were (mean+/-SEM) 55.7+/-2.2 and 49.3+/-7.6%, respectively; and the sperm CK-M ratios in the caput epididymidis of three men were 72, 75, and 70%, values that are similar to those of ejaculated sperm. In four segments of the proximal and distal epididymis of three stallions (the origin of sperm was also verified by the position of the cytoplasmic droplet) and in ejaculate of five stallions, the incidences of mature sperm were 88.2+/-6.2, 89.0+/-6.7, 90.3+/-7.8, 87.6+/-5.9, and 86.7+/-0.8%, and the respective CK-M ratios were 75.0+/-8.7, 84.2+/-2.9, 87.9+/-1.2, 92.5+/-1.5, and 69.3+/-3.5%. There were no differences in the incidences of mature and immature spermatozoa or in CK-M ratios among sperm arising from the various epididymal regions or from the ejaculate in men or stallions. Thus, the cellular maturation events in sperm, as detected by the CK markers, are completed by the time the sperm commences epididymal transport. These findings are in agreement with the IVF fertility of sperm aspirated from the male reproductive tract. The data may also suggest that the primary role of sperm epididymal transport in men is to remodel the plasma membrane to enhance sperm functional integrity in the diverse environments of the male and female reproductive tracts prior to fertilization.
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The research investigates the connection between epididymal sperm transport and fertility, focusing on the changes in sperm creative kinase (CK) values during epididymal transport. The study found that maturation events in sperm, monitored using CK markers, are completed before the sperm commences epididymal transport.
Objective and Method
The research aims to understand the relationship between epididymal sperm transport and sperm maturity in human and stallion spermatozoa. The two key features studied are creatine kinase (CK) concentrations, which indicate immature sperm via cytoplasmic retention, and the ratio between CK-M and CK-B isoforms, which is indicative of mature sperm.
To achieve this, the researchers examined whether changes in CK values are still ongoing during epididymal transport or if the maturation is complete prior to the arrival of sperm in the caput epididymidis. The observation involved human sperm from caput and corpus epididymis as well as stallion sperm from various epididymal regions and the ejaculate.
Findings
The research found no differences in the incidences of mature and immature spermatozoa or in CK-M ratios among sperm arising from the various epididymal regions or from the ejaculate in men or stallions. This suggests that maturation events in sperm, as detected by the CK markers, are completed by the time the sperm commence epididymal transport.
These results align with the known fertility of sperm aspirated from the male reproductive tract, used in in vitro fertilization, even if the sperm are recovered from the caput epididymidis or the rete testis. Thus, the data may imply that the main role of sperm epididymal transport in men is to remodel the plasma membrane to enhance sperm functional integrity in the diverse environments of the male and female reproductive tracts before fertilization occurs.
Implication
The findings reveal that the cellular maturation in sperm, detected using CK markers, is completed before the sperm start their journey through the epididymis, debunking any previous assumptions of ongoing maturation during the travel.
These results add to our understanding of human and animal fertility, and may guide future developments in fertility treatments and technologies.
Cite This Article
APA
Huszar G, Patrizio P, Vigue L, Willets M, Wilker C, Adhoot D, Johnson L.
(1998).
Cytoplasmic extrusion and the switch from creatine kinase B to M isoform are completed by the commencement of epididymal transport in human and stallion spermatozoa.
J Androl, 19(1), 11-20.
Department of Obstetrics and Gynecology, Yale University School of Medicine, New Haven, Connecticut 06525, USA.
Patrizio, P
Vigue, L
Willets, M
Wilker, C
Adhoot, D
Johnson, L
MeSH Terms
Animals
Creatine Kinase / metabolism
Cytoplasm / enzymology
Epididymis / physiology
Horses
Humans
Immunohistochemistry
Isoenzymes
Male
Sperm Motility
Spermatozoa / enzymology
Grant Funding
HD-19505 / NICHD NIH HHS
HD-39209 / NICHD NIH HHS
Citations
This article has been cited 9 times.
Butler ML, Hartman AR, Bormann JM, Weaber RL, Grieger DM, Rolf MM. Genome-wide association study of beef bull semen attributes. BMC Genomics 2022 Jan 23;23(1):74.
Scieglinska D, Krawczyk Z. Expression, function, and regulation of the testis-enriched heat shock HSPA2 gene in rodents and humans. Cell Stress Chaperones 2015 Mar;20(2):221-35.
Sati L, Cayli S, Delpiano E, Sakkas D, Huszar G. The pattern of tyrosine phosphorylation in human sperm in response to binding to zona pellucida or hyaluronic acid. Reprod Sci 2014 May;21(5):573-81.
Rengan AK, Agarwal A, van der Linde M, du Plessis SS. An investigation of excess residual cytoplasm in human spermatozoa and its distinction from the cytoplasmic droplet. Reprod Biol Endocrinol 2012 Nov 17;10:92.
Petersen CG, Massaro FC, Mauri AL, Oliveira JB, Baruffi RL, Franco JG Jr. Efficacy of hyaluronic acid binding assay in selecting motile spermatozoa with normal morphology at high magnification. Reprod Biol Endocrinol 2010 Dec 3;8:149.
Rago V, Siciliano L, Aquila S, Carpino A. Detection of estrogen receptors ER-alpha and ER-beta in human ejaculated immature spermatozoa with excess residual cytoplasm. Reprod Biol Endocrinol 2006 Jul 17;4:36.