A mouse seminal vesicle‐secreted lysozyme c‐like protein modulates sperm capacitation

Seminal vesicle proteins SVS3 and SVS4 facilitate SVS2 effect on sperm capacitation

Reproduction ◽

10.1530/rep-15-0551 ◽

2016 ◽

Vol 152 (4) ◽

pp. 313-321 ◽

Cited By ~ 8

Author(s):

Naoya Araki ◽

Natsuko Kawano ◽

Woojin Kang ◽

Kenji Miyado ◽

Kaoru Yoshida ◽

...

Keyword(s):

Seminal Vesicle ◽

Reproductive Tract ◽

Female Reproductive Tract ◽

The Other ◽

Sperm Capacitation ◽

Other Hand ◽

Sperm Membrane ◽

Vesicle Secretion ◽

Mammalian Spermatozoa

Mammalian spermatozoa acquire their fertilizing ability in the female reproductive tract (sperm capacitation). On the other hand, seminal vesicle secretion, which is a major component of seminal plasma, inhibits the initiation of sperm capacitation (capacitation inhibition) and reduces the fertility of the capacitated spermatozoa (decapacitation). There are seven major proteins involved in murine seminal vesicle secretion (SVS1-7), and we have previously shown that SVS2 acts as both a capacitation inhibitor and a decapacitation factor, and is indispensable forin vivofertilization. However, the effects of SVSs other than SVS2 on the sperm have not been elucidated. Since mouseSvs2–Svs6genes evolved by gene duplication belong to the same gene family, it is possible that SVSs other than SVS2 also have some effects on sperm capacitation. In this study, we examined the effects of SVS3 and SVS4 on sperm capacitation. Our results showed that both SVS3 and SVS4 are able to bind to spermatozoa, but SVS3 alone showed no effects on sperm capacitation. On the other hand, SVS4 acted as a capacitation inhibitor, although it did not show decapacitation abilities. Interestingly, SVS3 showed an affinity for SVS2 and it facilitated the effects of SVS2. Interaction of SVS2 and spermatozoa is mediated by the ganglioside GM1 in the sperm membrane; however, both SVS3 and SVS4 had weaker affinities for GM1 than SVS2. Therefore, we suggest that separate processes may cause capacitation inhibition and decapacitation, and SVS3 and SVS4 act on sperm capacitation cooperatively with SVS2.

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A Seminal Vesicle Autoantigen of Mouse Is Able to Suppress Sperm Capacitation-Related Events Stimulated by Serum Albumin1

Biology of Reproduction ◽

10.1095/biolreprod63.5.1562 ◽

2000 ◽

Vol 63 (5) ◽

pp. 1562-1566 ◽

Cited By ~ 40

Author(s):

Yen-Hua Huang ◽

Sin-Tak Chu ◽

Yee-Hsiung Chen

Keyword(s):

Seminal Vesicle ◽

Sperm Capacitation

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Suppression effect of seminal vesicle autoantigen on platelet-activating factor-induced mouse sperm capacitation

Journal of Cellular Biochemistry ◽

10.1002/jcb.21050 ◽

2007 ◽

Vol 100 (4) ◽

pp. 941-951 ◽

Cited By ~ 8

Author(s):

Yen Hua Huang ◽

Yee Hsiung Chen ◽

Chun Mao Lin ◽

Yi Yun Ciou ◽

Shin Peih Kuo ◽

...

Keyword(s):

Seminal Vesicle ◽

Platelet Activating Factor ◽

Sperm Capacitation ◽

Mouse Sperm ◽

Suppression Effect

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Seminal Vesicle Secretion 2 Acts as a Protectant of Sperm Sterols and Prevents Ectopic Sperm Capacitation in Mice1

Biology of Reproduction ◽

10.1095/biolreprod.114.120642 ◽

2015 ◽

Vol 92 (1) ◽

Cited By ~ 19

Author(s):

Naoya Araki ◽

György Trencsényi ◽

Zoárd T. Krasznai ◽

Enikő Nizsalóczki ◽

Ayako Sakamoto ◽

...

Keyword(s):

Seminal Vesicle ◽

Sperm Capacitation ◽

Vesicle Secretion

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SPINKL, a Kazal-type serine protease inhibitor-like protein purified from mouse seminal vesicle fluid, is able to inhibit sperm capacitation

Reproduction ◽

10.1530/rep-07-0375 ◽

2008 ◽

Vol 136 (5) ◽

pp. 559-571 ◽

Cited By ~ 34

Author(s):

Ming-Huei Lin ◽

Robert Kuo-Kuang Lee ◽

Yuh-Ming Hwu ◽

Chung-Hao Lu ◽

Shian-Ling Chu ◽

...

Keyword(s):

Ion Exchange ◽

Protease Inhibitor ◽

Seminal Vesicle ◽

Serine Protease ◽

Serine Protease Inhibitor ◽

Exchange Chromatography ◽

Seminal Vesicles ◽

Sperm Capacitation ◽

Anion Exchange Column

We report a secreted serine protease inhibitor Kazal-type-like (SPINKL) protein. The SPINKL protein was purified from mouse seminal vesicle secretions through a series of steps, including ion-exchange chromatography on a diethylaminoethyl-Sephacel column, gel filtration on a Sephadex G-75 column, and ion-exchange HPLC on a Q strong anion exchange column. Further analysis identified several SPINKL proteins with various N-linked carbohydrates. The SPINKL protein has six conserved cysteine residues that are nearly identical to those of members of the SPINK protein family. It was noted that the SPINKL protein showed no inhibitory activities against common serine proteases such as trypsin, chymotrypsin, subtilisin, or elastase.SpinklmRNA and SPINKL proteins were found to be primarily expressed in seminal vesicles. Immunohistochemistry revealed that the SPINKL protein occurred in the luminal fluid and mucosal epithelium of the seminal vesicles and was regulated by testosterone. The SPINKL protein was able to bind onto sperm and enhance sperm motility. Also, it was able to suppress BSA-stimulated sperm capacitation and block sperm–oocyte interactionsin vitro, suggesting that SPINKL may be a decapacitation factor.

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Electron Microscopic Study of the Epithelium of the Seminal Vesicle of Aging Rats

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100050706 ◽

1974 ◽

Vol 32 ◽

pp. 138-139

Author(s):

V. F. Allison ◽

G. C. Fink ◽

G. W. Cearley

Keyword(s):

Cell Growth ◽

Epithelial Cell ◽

Epithelial Cells ◽

Seminal Vesicle ◽

Seminal Vesicles ◽

Epithelial Layer ◽

Epithelial Hyperplasia ◽

Electron Microscopic ◽

Aging Rats ◽

Pseudostratified Epithelium

It is well known that epithelial hyperplasia (benign hypertrophy) is common in the aging prostate of dogs and man. In contrast, little evidence is available for abnormal epithelial cell growth in seminal vesicles of aging animals. Recently, enlarged seminal vesicles were reported in senescent mice, however, that enlargement resulted from increased storage of secretion in the lumen and occurred concomitant to epithelial hypoplasia in that species.The present study is concerned with electron microscopic observations of changes occurring in the pseudostratified epithelium of the seminal vescles of aging rats. Special attention is given to certain non-epithelial cells which have entered the epithelial layer.

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The Effect of Androgen Depletion and Replacement on the Epithelium of the Seminal Vesicle of the Aging Rat

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100116577 ◽

1975 ◽

Vol 33 ◽

pp. 590-591

Author(s):

Venita F. Allison

Keyword(s):

Cell Proliferation ◽

Seminal Vesicle ◽

Male Rats ◽

Target Cells ◽

Cell Regeneration ◽

Secretory Function ◽

Electron Microscopic ◽

Aging Rat ◽

Microscopic Studies ◽

Androgen Depletion

In 1930, Moore, Hughes and Gallager reported that after castration seminal vesicle epithelial cell atrophy occurred and that cell regeneration could be achieved with daily injections of testis extract. Electron microscopic studies have confirmed those observations and have shown that testosterone injections restore the epithelium of the seminal vesicle in adult castrated male rats. Studies concerned with the metabolism of androgens point out that dihydrotestosterone stimulates cell proliferation and that other metabolites of testosterone probably influence secretory function in certain target cells.Although the influence of androgens on adult seminal vesicle epithelial cytology is well documented, little is known of the effect of androgen depletion and replacement on those cells in aging animals. The present study is concerned with the effect of castration and testosterone injection on the epithelium of the seminal vesicle of aging rats.

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Fine structure and possible functions of the hermaphrodite duct of some pulmonate snails (Mollusca: Gastropoda)

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100157887 ◽

1990 ◽

Vol 48 (3) ◽

pp. 68-69

Author(s):

Alan N. Hodgson

Keyword(s):

Electron Microscopy ◽

Transmission Electron Microscopy ◽

Fine Structure ◽

Seminal Vesicle ◽

Reproductive Biology ◽

Light Microscope ◽

Light Microscope Level ◽

Transmission Electron ◽

Standard Techniques

The hermaphrodite duct of pulmonate snails connects the ovotestis to the fertilization pouch. The duct is typically divided into three zones; aproximal duct which leaves the ovotestis, the middle duct (seminal vesicle) and the distal ovotestis duct. The seminal vesicle forms the major portion of the duct and is thought to store sperm prior to copulation. In addition the duct may also play a role in sperm maturation and degredation. Although the structure of the seminal vesicle has been described for a number of snails at the light microscope level there appear to be only two descriptions of the ultrastructure of this tissue. Clearly if the role of the hermaphrodite duct in the reproductive biology of pulmonatesis to be understood, knowledge of its fine structure is required.Hermaphrodite ducts, both containing and lacking sperm, of species of the terrestrial pulmonate genera Sphincterochila, Levantina, and Helix and the marine pulmonate genus Siphonaria were prepared for transmission electron microscopy by standard techniques.

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