Altered epididymal sperm maturation and cytoplasmic droplet migration in subfertile male Alox15 mice

2010 ◽  
Vol 340 (3) ◽  
pp. 569-581 ◽  
Author(s):  
Kelly Moore ◽  
Kyle Lovercamp ◽  
Dongyan Feng ◽  
Jennifer Antelman ◽  
Miriam Sutovsky ◽  
...  
2021 ◽  
Vol 548 ◽  
pp. 7-13
Author(s):  
Zongzhuang Wen ◽  
Dongyue Liu ◽  
Haixia Zhu ◽  
Xiaoyang Sun ◽  
Yu Xiao ◽  
...  

Open Biology ◽  
2015 ◽  
Vol 5 (8) ◽  
pp. 150080 ◽  
Author(s):  
Catherine E. Au ◽  
Louis Hermo ◽  
Elliot Byrne ◽  
Jeffrey Smirle ◽  
Ali Fazel ◽  
...  

Discovered in 1909 by Retzius and described mainly by morphology, the cytoplasmic droplet of sperm (renamed here the Hermes body) is conserved among all mammalian species but largely undefined at the molecular level. Tandem mass spectrometry of the isolated Hermes body from rat epididymal sperm characterized 1511 proteins, 43 of which were localized to the structure in situ by light microscopy and two by quantitative electron microscopy localization. Glucose transporter 3 (GLUT-3) glycolytic enzymes, selected membrane traffic and cytoskeletal proteins were highly abundant and concentrated in the Hermes body. By electron microscope gold antibody labelling, the Golgi trafficking protein TMED7/p27 localized to unstacked flattened cisternae of the Hermes body, as did GLUT-3, the most abundant protein. Its biogenesis was deduced through the mapping of protein expression for all 43 proteins during male germ cell differentiation in the testis. It is at the terminal step 19 of spermiogenesis that the 43 characteristic proteins accumulated in the nascent Hermes body.


2018 ◽  
Vol 24 (3) ◽  
pp. 111-122 ◽  
Author(s):  
Jinghua Hu ◽  
D Jo Merriner ◽  
Anne E O’Connor ◽  
Brendan J Houston ◽  
Luc Furic ◽  
...  

2015 ◽  
Vol 113 ◽  
pp. 226-243 ◽  
Author(s):  
Valérie Labas ◽  
Lucie Spina ◽  
Clémence Belleannee ◽  
Ana-Paula Teixeira-Gomes ◽  
Audrey Gargaros ◽  
...  

1994 ◽  
Vol 17 (5) ◽  
pp. 256-261 ◽  
Author(s):  
R. WEISSENBERG ◽  
S. YOSSEFI ◽  
Y. OSCHRY ◽  
I. MADGAR ◽  
L. M. LEWIN

Author(s):  
Louis Hermo ◽  
Regiana L. Oliveira ◽  
Charles E. Smith ◽  
John J.M. Bergeron

Reproduction ◽  
2009 ◽  
Vol 137 (3) ◽  
pp. 379-389 ◽  
Author(s):  
P Sipilä ◽  
J Jalkanen ◽  
I T Huhtaniemi ◽  
M Poutanen

Apart from condoms and vasectomy, modern contraceptive methods for men are still not available. Besides hormonal approaches to stop testicular sperm production, the post-meiotic blockage of epididymal sperm maturation carries lots of promise. Microarray and proteomics techniques and libraries of expressed sequence tags, in combination with digital differential display tools and publicly available gene expression databases, are being currently used to identify and characterize novel epididymal proteins as putative targets for male contraception. The data reported indicate that these technologies provide complementary information for the identification of novel highly expressed genes in the epididymis. Deleting the gene of interest by targeted ablation technology in mice or using immunization against the cognate protein are the two preferred methods to functionally validate the function of novel genesin vivo. In this review, we summarize the current knowledge of several epididymal proteins shown eitherin vivoorin vitroto be involved in the epididymal sperm maturation. These proteins include CRISP1, SPAG11e, DEFB126, carbonyl reductase P34H, CD52, and GPR64. In addition, we introduce novel proteinases and protease inhibitor gene families with potentially important roles in regulating the sperm maturation process. Furthermore, potential contraceptive strategies as well as delivery methods will be discussed. Despite the progress made in recent years, further studies are needed to reveal further details in the epididymal sperm maturation process and the factors involved, in order to facilitate the development of new epididymal contraceptives.


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