Literature DB >> 12297107

Hyperactivated motility of bull sperm is triggered at the axoneme by Ca2+ and not cAMP.

Han-Chen Ho1, Katherine A Granish, Susan S Suarez.   

Abstract

Hyperactivated motility, a swimming pattern of mammalian sperm in the oviduct, is essential for fertilization in vivo. It is characterized by high-amplitude flagellar waves and, usually, highly asymmetrical flagellar beating. It had been suggested, but not tested, that Ca2+ and cAMP switch on hyperactivation by directly affecting the flagellar axoneme. In this study, the direct affects of these agents on the axoneme were tested by using detergent-demembranated bull sperm. As confirmed by TEM, treatment of sperm with 0.2% Triton X-100 disrupted the plasma, acrosomal, and inner mitochondrial membranes, leaving axonemes intact. In the presence of 2 mM ATP, the percentage of reactivated sperm that were hyperactivated increased to 80% when free Ca2+ was increased from 50 to 400 nM. The effect of the Ca2+ in this range was to increase beat asymmetry by increasing the curvature of the principal bend. No additional increases were observed above 400 nM free Ca2+, but motility was suppressed at 1 mM. The ability of Ca2+ to produce hyperactivation depended on ATP availability, such that more ATP was required to produce the high amplitude flagellar bends characteristic of hyperactivated motility than to produce activated motility. Cyclic AMP was not required for reactivation, nor for hyperactivation. Production of hyperactivated motility also required an alkaline environment (pH 7.9-8.5). These results suggest that, provided sufficient ATP is present and pH is sufficiently alkaline, Ca2+ switches on hyperactivation by enabling curvature of the principal bends to increase.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12297107     DOI: 10.1006/dbio.2002.0797

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  65 in total

1.  Hyperactivated sperm motility driven by CatSper2 is required for fertilization.

Authors:  Timothy A Quill; Sarah A Sugden; Kristen L Rossi; Lynda K Doolittle; Robert E Hammer; David L Garbers
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-01       Impact factor: 11.205

2.  Regulation of fertilization in male rats by CatSper2 knockdown.

Authors:  Zhen Zhang; Gen-Lin Wang; Hui-Xia Li; Lian Li; Qun-Wei Cui; Cheng-Bin Wei; Fei Zhou
Journal:  Asian J Androl       Date:  2011-10-17       Impact factor: 3.285

Review 3.  Rethinking the relationship between hyperactivation and chemotaxis in mammalian sperm.

Authors:  Haixin Chang; Susan S Suarez
Journal:  Biol Reprod       Date:  2010-05-12       Impact factor: 4.285

4.  The flagellar protein Enkurin is required for mouse sperm motility and for transport through the female reproductive tract.

Authors:  Melissa K Jungnickel; Keith A Sutton; Mark A Baker; Michael G Cohen; Michael J Sanderson; Harvey M Florman
Journal:  Biol Reprod       Date:  2018-10-01       Impact factor: 4.285

5.  The "soluble" adenylyl cyclase in sperm mediates multiple signaling events required for fertilization.

Authors:  Kenneth C Hess; Brian H Jones; Becky Marquez; Yanqiu Chen; Teri S Ord; Margarita Kamenetsky; Catarina Miyamoto; Jonathan H Zippin; Gregory S Kopf; Susan S Suarez; Lonny R Levin; Carmen J Williams; Jochen Buck; Stuart B Moss
Journal:  Dev Cell       Date:  2005-08       Impact factor: 12.270

6.  All four CatSper ion channel proteins are required for male fertility and sperm cell hyperactivated motility.

Authors:  Huayu Qi; Magdalene M Moran; Betsy Navarro; Jayhong A Chong; Grigory Krapivinsky; Luba Krapivinsky; Yuriy Kirichok; I Scott Ramsey; Timothy A Quill; David E Clapham
Journal:  Proc Natl Acad Sci U S A       Date:  2007-01-16       Impact factor: 11.205

7.  Extracellular adenosine 5'-triphosphate alters motility and improves the fertilizing capability of mouse sperm.

Authors:  Esmeralda Rodríguez-Miranda; Mariano G Buffone; Scott E Edwards; Teri S Ord; Kathleen Lin; Mary D Sammel; George L Gerton; Stuart B Moss; Carmen J Williams
Journal:  Biol Reprod       Date:  2008-04-09       Impact factor: 4.285

8.  Contributions of extracellular and intracellular Ca2+ to regulation of sperm motility: Release of intracellular stores can hyperactivate CatSper1 and CatSper2 null sperm.

Authors:  Becky Marquez; George Ignotz; Susan S Suarez
Journal:  Dev Biol       Date:  2006-11-10       Impact factor: 3.582

9.  Intracellular translocation and differential accumulation of cell-penetrating peptides in bovine spermatozoa: evaluation of efficient delivery vectors that do not compromise human sperm motility.

Authors:  Sarah Jones; Monika Lukanowska; Julia Suhorutsenko; Senga Oxenham; Christopher Barratt; Steven Publicover; Dana Maria Copolovici; Ülo Langel; John Howl
Journal:  Hum Reprod       Date:  2013-04-12       Impact factor: 6.918

10.  Characterization of 3-hydroxyisobutyrate dehydrogenase, HIBADH, as a sperm-motility marker.

Authors:  Yung-Chieh Tasi; Hsin-Chih Albert Chao; Chia-Ling Chung; Xiu-Ying Liu; Ying-Ming Lin; Pao-Chi Liao; Hsien-An Pan; Han-Sun Chiang; Pao-Lin Kuo; Ying-Hung Lin
Journal:  J Assist Reprod Genet       Date:  2013-02-20       Impact factor: 3.412

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.