scholarly journals Faculty Opinions recommendation of A new insight into male fertility preservation for patients with completely immotile spermatozoa.

Author(s):  
Paul Turek
Author(s):  
Huanhua Chen ◽  
Guixue Feng ◽  
Bo Zhang ◽  
Hong Zhou ◽  
Caizhu Wang ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-13 ◽  
Author(s):  
Md Saidur Rahman ◽  
Woo-Sung Kwon ◽  
Myung-Geol Pang

Freshly ejaculated spermatozoa are incapable or poorly capable of fertilizing an oocyte. The fertilization aptness of spermatozoa depends on the appropriate and time-dependent acquisition of hyperactivation, chemotaxis, capacitation, and the acrosome reaction, where calcium (Ca2+) is extensively involved in almost every step. A literature review showed that several ion channel proteins are likely responsible for regulation of the Ca2+uptake in spermatozoa. Therefore, manipulation of the functions of channel proteins is closely related to Ca2+influx, ultimately affecting male fertility. Recently, it has been shown that, together with different physiological stimuli, protein-protein interaction also modifies the Ca2+influx mechanism in spermatozoa. Modern proteomic analyses have identified several sperm proteins, and, therefore, these findings might provide further insight into understanding the Ca2+influx, protein functions, and regulation of fertility. The objective of this review was to synthesize the published findings on the Ca2+influx mechanism in mammalian spermatozoa and its implications for the regulation of male fertility in the context of sperm proteins. Finally, Pathway Studio (9.0) was used to catalog the sperm proteins that regulate the Ca2+influx signaling by using the information available from the PubMed database following a MedScan Reader (5.0) search.


Cryobiology ◽  
2020 ◽  
Vol 95 ◽  
pp. 1-8 ◽  
Author(s):  
Tie-Cheng Sun ◽  
Hui-Ying Li ◽  
Xiao-Yu Li ◽  
Kun Yu ◽  
Shou-Long Deng ◽  
...  

Niche Journal ◽  
2013 ◽  
Vol 1 (2) ◽  
pp. 42-45 ◽  
Author(s):  
Beril Yuksel ◽  
Sevtap Kilic ◽  
Figen Taser ◽  
Ferda Alparslan Pinarli ◽  
Tuncay Delibasi

Reproduction ◽  
2009 ◽  
Vol 138 (4) ◽  
pp. 655-666 ◽  
Author(s):  
Yongmei Chen ◽  
Huizhen Wang ◽  
Nan Qi ◽  
Hui Wu ◽  
Weipeng Xiong ◽  
...  

Mice lacking TYRO3, AXL and MER (TAM) receptor tyrosine kinases (RTKs) are male sterile. The mechanism of TAM RTKs in regulating male fertility remains unknown. In this study, we analyzed in more detail the testicular phenotype of TAM triple mutant (TAM−/−) mice with an effort to understand the mechanism. We demonstrate that the three TAM RTKs cooperatively regulate male fertility, and MER appears to be more important than AXL and TYRO3. TAM−/− testes showed a progressive loss of germ cells from elongated spermatids to spermatogonia. Young adult TAM−/− mice exhibited oligo-astheno-teratozoospermia and various morphological malformations of sperm cells. As the mice aged, the germ cells were eventually depleted from the seminiferous tubules. Furthermore, we found that TAM−/− Sertoli cells have an impaired phagocytic activity and a large number of differentially expressed genes compared to wild-type controls. By contrast, the function of Leydig cells was not apparently affected by the mutation of TAM RTKs. Therefore, we conclude that the suboptimal function of Sertoli cells leads to the impaired spermatogenesis in TAM−/− mice. The results provide novel insight into the mechanism of TAM RTKs in regulating male fertility.


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