scholarly journals Sperm Release at Spermiation Is Regulated by Changes in the Organization of Actin- and Microtubule-Based Cytoskeletons at the Apical Ectoplasmic Specialization—A Study Using the Adjudin Model

Endocrinology ◽  
2017 ◽  
Vol 158 (12) ◽  
pp. 4300-4316 ◽  
Author(s):  
Linxi Li ◽  
Elizabeth I Tang ◽  
Haiqi Chen ◽  
Qingquan Lian ◽  
Renshan Ge ◽  
...  
2021 ◽  
Vol 99 (Supplement_1) ◽  
pp. 113-114
Author(s):  
David J Miller

Abstract Because mating is not always synchronized with ovulation, females from many species store sperm in the female reproductive tract until ovulation and fertilization. This may be done for short periods, a day or two for swine and cattle, or longer periods. Other mammals, such as some species of bats, store sperm for several months. Chickens and turkeys store sperm for 2–4 weeks and queens of some species of insects store sperm for over a decade in specialized structures. How sperm are retained, kept fertile for varying times and released is unclear. We have identified two specific carbohydrate motifs that are abundant in the porcine oviduct that bind and retain sperm in the isthmus. When immobilized, these two glycans lengthen sperm lifespan and suppress the normal increase in intracellular Ca2+ that normally accompanies capacitation. Porcine sperm can be released from oviduct cells and immobilized glycans by progesterone, perhaps of ovarian or cumulus-oocyte complex origin, which activates CatSper, a sperm-specific Ca2+ channel. Progesterone, as well as other compounds that stimulate hyperactivated motility, trigger sperm release, suggesting that hyperactivated motility is sufficient to release porcine sperm from oviduct glycans. We also have found that blocking proteasome-induced sperm protein lysis diminishes the number of sperm released from oviduct glycans. Finally, a transcriptomic approach has identified several groups of genes that are differentially regulated in both bovine and porcine oviducts from estrus animals that are storing sperm compared to oviducts from diestrus animals. This provides clues about how sperm lifespan is extended during storage.


2005 ◽  
Vol 65 (1) ◽  
pp. 29-41 ◽  
Author(s):  
H. K. Boscolo ◽  
F. L. Silveira

The reproductive biology of Palythoa caribaeorum (Duchassaing & Michelotti 1860) and Protopalythoa variabilis (Duerden 1898) was studied through monthly samples from tagged colonies from June 1996 to June 1997, in São Sebastião channel, São Paulo, Brazil (45º26'W, 23º50'S). The gametogenesis was similar to that of other zoanthids as shown by histological preparations. Oocyte diameters and maturation stages of testis vesicles were evaluated on squash preparations. Both species showed sequential protogynic hermaphroditism, with high frequency of fertile polyps (83% in P. variabilis and 72% in P. caribaeorum), high frequency of colonies in female sex condition (65.3% of P. variabilis and 41.7% of P. caribaeorum), and apparently continuous gametogenesis. In P. caribaeorum, egg release was continuous and sperm release took place during half of the analyzed period. In P. variabilis, egg and sperm release occurred in April-May and February-March 1997, respectively.


2013 ◽  
Vol 305 (6) ◽  
pp. E687-E699 ◽  
Author(s):  
Hin-Ting Wan ◽  
Dolores D. Mruk ◽  
Stephen Y. T. Li ◽  
Ka-Wai Mok ◽  
Will M. Lee ◽  
...  

During spermatogenesis, the molecular mechanism that confers spermatid adhesion to the Sertoli cell at the apical ectoplasmic specialization (apical ES), a testis-specific F-actin-rich adherens junction, in the rat testis remains elusive. Herein, the activated form of focal adhesion kinase (FAK), p-FAK-Tyr397, a component of the apical ES that was expressed predominantly and stage specifically in stage VII-early stage VIII tubules, was found to be a crucial apical ES regulator. Using an FAK-Y397E phosphomimetic mutant cloned in a mammalian expression vector for its transfection vs. FAK and vector alone in adult rat testes in vivo, its overexpression was found to cause defects in spermiation. These defects in spermiation were manifested by entrapment of spermatids in the seminiferous epithelium in late stage VIII–X tubules and were mediated by a disruption on the spatiotemporal expression and/or mislocalization of actin regulatory protein actin-related protein 3, which induces branched actin polymerization, epidermal growth factor receptor pathway substrate 8 (an actin barbed end capping and bundling protein), and palladin (an actin cross-linking and bundling protein). This thus perturbed changes of F-actin organization at the apical ES to facilitate spermiation, which also led to a concomitant alteration in the distribution and upregulation of adhesion proteins nectin-2 and nectin-3 at the apical ES. As such, nectin-2 and -3 remained at the apical ES to anchor step 19 spermatids on to the epithelium, delaying spermiation. These findings illustrate a mechanistic pathway mediated by p-FAK-Tyr397 that regulates spermatid adhesion at the apical ES in vivo.


2019 ◽  
Vol 6 ◽  
Author(s):  
Hillary A. Smith ◽  
Aurelie Moya ◽  
Neal E. Cantin ◽  
Madeleine J. H. van Oppen ◽  
Gergely Torda

Biology Open ◽  
2019 ◽  
Vol 8 (2) ◽  
pp. bio036939 ◽  
Author(s):  
Pankaj Dubey ◽  
Tushna Kapoor ◽  
Samir Gupta ◽  
Seema Shirolikar ◽  
Krishanu Ray

2003 ◽  
Vol 20 (5) ◽  
pp. 809-821 ◽  
Author(s):  
Zdenka Syrova ◽  
Ivo Sauman ◽  
Jadwiga M. Giebultowicz

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