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  Rotational motion and rheotaxis of human sperm do not require functional CatSper channels and transmembrane Ca2+ signaling.

Schiffer, C., Rieger, S., Brenker, C., Young, S., Hamzeh, H., Wachten, D., et al. (2020). Rotational motion and rheotaxis of human sperm do not require functional CatSper channels and transmembrane Ca2+ signaling. The EMBO Journal, 39(4): e102363. doi:10.15252/embj.2019102363.

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Schiffer_et_al-2020-The_EMBO_Journal.pdf (Publisher version), 3MB
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Schiffer_et_al-2020-The_EMBO_Journal.pdf
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 Creators:
Schiffer, Christian1, Author           
Rieger, Steffen1, Author
Brenker, Christoph1, Author
Young, Samuel1, Author
Hamzeh, Hussein2, Author
Wachten, Dagmar3, Author           
Tüttelmann, Frank1, Author
Röpke, Albrecht1, Author
Kaupp, Ulrich Benjamin2, Author           
Wang, Tao1, Author
Wagner, Alice1, Author
Krallmann, Claudia1, Author
Kliesch, Sabine1, Author
Fallnich, Carsten1, Author
Strünker, Timo1, Author
Affiliations:
1External Organizations, ou_persistent22              
2Department of Molecular Sensory Systems, Center of Advanced European Studies and Research (caesar), Max Planck Society, ou_2173679              
3Max Planck Research Group Molecular Physiology, Center of Advanced European Studies and Research (caesar), Max Planck Society, ou_2173682              

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Free keywords: Ca2+ signaling; CatSper; human sperm; rheotaxis; rolling
 Abstract: Navigation of sperm in fluid flow, called rheotaxis, provides long-range guidance in the mammalian oviduct. The rotation of sperm around their longitudinal axis (rolling) promotes rheotaxis. Whether sperm rolling and rheotaxis require calcium (Ca2+ ) influx via the sperm-specific Ca2+ channel CatSper, or rather represent passive biomechanical and hydrodynamic processes, has remained controversial. Here, we study the swimming behavior of sperm from healthy donors and from infertile patients that lack functional CatSper channels, using dark-field microscopy, optical tweezers, and microfluidics. We demonstrate that rolling and rheotaxis persist in CatSper-deficient human sperm. Furthermore, human sperm undergo rolling and rheotaxis even when Ca2+ influx is prevented. Finally, we show that rolling and rheotaxis also persist in mouse sperm deficient in both CatSper and flagellar Ca2+ -signaling domains. Our results strongly support the concept that passive biomechanical and hydrodynamic processes enable sperm rolling and rheotaxis, rather than calcium signaling mediated by CatSper or other mechanisms controlling transmembrane Ca2+ flux.

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Language(s): eng - English
 Dates: 2020-01-192020-02-17
 Publication Status: Issued
 Pages: 15
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.15252/embj.2019102363
 Degree: -

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Title: The EMBO Journal
  Abbreviation : EMBO J.
Source Genre: Journal
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Publ. Info: Nature Publishing Group
Pages: - Volume / Issue: 39 (4) Sequence Number: e102363 Start / End Page: - Identifier: ISSN: 0261-4189
CoNE: https://pure.mpg.de/cone/journals/resource/954925497061_1