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© 2016. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.

Abstract

Sperm motility is driven by motile cytoskeletal elements in the tail, called axonemes. The structure of axonemes consists of 9 + 2 microtubules, molecular motors (dyneins), and their regulatory structures. Axonemes are well conserved in motile cilia and flagella through eukaryotic evolution. Deficiency in the axonemal structure causes defects in sperm motility, and often leads to male infertility. It has been known since the 1970s that, in some cases, male infertility is linked with other symptoms or diseases such as Kartagener syndrome. Given that these links are mostly caused by deficiencies in the common components of cilia and flagella, they are called “immotile cilia syndrome” or “primary ciliary dyskinesia,” or more recently, “ciliopathy,” which includes deficiencies in primary and sensory cilia. Here, we review the structure of the sperm flagellum and epithelial cilia in the human body, and discuss how male fertility is linked to ciliopathy.

Details

Title
Sperm dysfunction and ciliopathy
Author
Inaba, Kazuo 1 ; Mizuno, Katsutoshi 2 

 Shimoda Marine Research Center, University of Tsukuba, Shizuoka, Japan 
 Shimoda Marine Research Center, University of Tsukuba, Shizuoka, Japan; Department of Biological Sciences, Dartmouth College, Hanover, NH, USA 
Pages
77-94
Section
Review Article
Publication year
2016
Publication date
Apr 2016
Publisher
John Wiley & Sons, Inc.
ISSN
14455781
e-ISSN
14470578
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3066202491
Copyright
© 2016. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.