Genetic influences on mouse sperm capacitation in vivo and in vitro

1980 ◽  
Vol 3 (4) ◽  
pp. 343-349 ◽  
Author(s):  
P. C. Hoppe
Keyword(s):  
Genetic Influences ◽  
Sperm Capacitation ◽  
Mouse Sperm

Mechanisms of displacement of sperm basic nuclear proteins in mammals. An in vitro simulation of post-fertilization results

1982 ◽  
Vol 53 (1) ◽  
pp. 227-244
Author(s):  
T.C. Rodman ◽  
F.H. Pruslin ◽  
V.G. Allfrey
Keyword(s):  
Sperm Nucleus ◽  
Nuclear Proteins ◽  
Mouse Sperm ◽  
Basic Proteins ◽  
Molecular Events ◽  
In Vitro Simulation ◽  
Sperm Nuclei ◽  
Two Parameters

A standardized cytological preparation of mature mouse sperm has been devised to serve as an in vitro system for probing the intra-ooplasmic molecular events of transformation of the fertilizing sperm. Two parameters of the early phase of transformation in vivo are defined at the resolution of the light microscope: deletion of sperm-unique nuclear proteins, detectable by immunofluorescence, and retention of homogeneity of the residual DNA complex, with intact chromatin boundaries detectable by ethidium bromide staining. These studies show that both parameters are conserved when in vitro sperm preparations are treated with NaCl under reducing conditions. The deletion of 2 different classes of the unique basic proteins of mouse sperm nuclei is specified by the NaCl concentration: 0.7 M-NaCl displaces the non-protamine class but not the protamines, while 1 M-NaCl displaces both. On the other hand the effects of treatment with trypsin at various concentrations and intervals are less consistent with the in vivo parameters, indicating fragmentation and displacement, not only of the sperm-unique basic proteins, but also of structural proteins believed to maintain the fundamental cohesive organization of the DNA matrix. These observations suggest that mechanisms other than proteolysis, e.g. localized changes in ionic concentrations, may participate in the post-fertilization displacement of the sperm-unique nuclear proteins in vivo. This study also supports the validity of the in vitro simulation as a model with which to probe the progression of transformation of the sperm nucleus to the zygote pronucleus.

scholarly journals In vivo exposure to 17β-estradiol triggers premature sperm capacitation in cauda epididymis

Reproduction ◽  
2013 ◽  
Vol 145 (3) ◽  
pp. 255-263 ◽  
Author(s):  
Lukas Ded ◽  
Natasa Sebkova ◽  
Martina Cerna ◽  
Fatima Elzeinova ◽  
Pavla Dostalova ◽  
...  
Keyword(s):  
Reproductive Tract ◽  
Negative Impact ◽  
Reproductive Potential ◽  
Female Reproductive Tract ◽  
Sperm Capacitation ◽  
Epididymal Sperm ◽  
Knock Out ◽  
17Β Estradiol

Estrogens play a crucial role in spermatogenesis and estrogen receptor α knock-out male mice are infertile. It has been demonstrated that estrogens significantly increase the speed of capacitation in vitro; however this may lead to the reduction of reproductive potential due to the decreased ability of these sperm to undergo the acrosome reaction. To date the in vivo effect of estrogens on the ability of sperm to capacitate has not been investigated. Therefore, in this study, we exposed mice (n=24) to 17β-estradiol (E2) at the concentration of 20 ng/ml either during puberty from the fourth to seventh week of age (n=8), or continuously from birth for a period of 12 weeks (n=8) at which age the animals from both groups were killed. The capacitation status of epididymal and testicular sperm was analysed by tyrosine phosphorylation (TyrP) antibody (immunofluorescence and western blot) and chlortetracycline (CTC) assay. According to our results, in vivo exposure to increased E2 concentrations caused premature sperm capacitation in the epididymis. The effect of E2, however, seems reversible because after the termination of the exposure premature epididymal sperm capacitation is decreased in animals treated during puberty. Furthermore the changes in epididymal sperm capacitation status detected by TyrP and CTC positively correlate with plasma levels of E2 and the expression of the estrogen-dependent trefoil factor 1 (Tff1) gene in testicular tissue. Therefore, our data implicate that in vivo exposure to E2 under specific conditions leads to the premature capacitation of mouse sperm in epididymis with a potential negative impact on the sperm reproductive fitness in the female reproductive tract.

ZP2 peptide beads that select human sperm in vitro, decoy mouse sperm in vivo, and provide reversible contraception

2016 ◽  
Vol 106 (3) ◽  
pp. e112
Author(s):  
M. Avella ◽  
B. Baibakov ◽  
A. Burkart Sadusky ◽  
J. Dean
Keyword(s):  
Human Sperm ◽  
Mouse Sperm

scholarly journals The slower the better: how sperm capacitation and acrosome reaction is modified in the presence of estrogens

Reproduction ◽  
2012 ◽  
Vol 143 (3) ◽  
pp. 297-307 ◽  
Author(s):  
Natasa Sebkova ◽  
Martina Cerna ◽  
Lukas Ded ◽  
Jana Peknicova ◽  
Katerina Dvorakova-Hortova
Keyword(s):  
Acrosome Reaction ◽  
Estrogen Receptor Beta ◽  
Calcium Ionophore ◽  
Membrane Receptors ◽  
Sperm Capacitation ◽  
Mouse Sperm ◽  
Synthetic Estrogens ◽  
Dependent Protein ◽  
Plasma Membrane Receptors

In order for mammalian sperm to obtain a fertilizing ability, they must undergo a complex of molecular changes, called capacitation. During capacitation, steroidal compounds can exert a fast nongenomic response in sperm through their interaction with plasma membrane receptors, and activate crucial signaling pathways leading to time-dependent protein tyrosine phosphorylation (TyrP). Estrogen receptor beta was detected in epididymal mouse sperm; therefore, the effect of 17B-estradiol, estrone, estriol, and 17A-ethynylestradiol on mouse sperm capacitation in vitro was investigated. The effect was evaluated by positive TyrP in sperm heads and in the whole sperm lysates. Simultaneously, the state of the acrosome after the calcium ionophore-induced acrosome reaction was assessed. Generally, estrogens displayed a time and concentration-dependent stimulatory effect on sperm TyrP during capacitation. In contrast, the number of sperm that underwent the acrosome reaction was lower in the experimental groups. It has been demonstrated that both natural and synthetic estrogens can modify the physiological progress of mouse sperm capacitation. The potential risk in the procapacitation effect of estrogens can also be seen in the decreased ability of sperm to undergo the acrosome reaction. In conclusion, the capacitating ability of sperm can be significantly lowered by increasing the level of estrogens in the environment.

scholarly journals ZP2 peptide beads select human sperm in vitro, decoy mouse sperm in vivo, and provide reversible contraception

2016 ◽  
Vol 8 (336) ◽  
pp. 336ra60-336ra60 ◽  
Author(s):  
Matteo A. Avella ◽  
Boris A. Baibakov ◽  
Maria Jimenez-Movilla ◽  
Anna Burkart Sadusky ◽  
Jurrien Dean
Keyword(s):  
Human Sperm ◽  
Mouse Sperm
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