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

https://doi.org/10.15252/embj.2019102363
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cyto.990050407openalex-snapshot
Rotational and translational swimming of human spermatozoa: A dynamic laser light scattering study
inferredcites →https://doi.org/10.1016/j.cell.2009.12.053openalex-snapshot
Acid Extrusion from Human Spermatozoa Is Mediated by Flagellar Voltage-Gated Proton Channel
inferredcites →https://doi.org/10.1016/j.cell.2014.02.056openalex-snapshot
Structurally Distinct Ca2+ Signaling Domains of Sperm Flagella Orchestrate Tyrosine Phosphorylation and Motility
inferredcites →https://doi.org/10.1016/j.cell.2019.03.047openalex-snapshot
Dual Sensing of Physiologic pH and Calcium by EFCAB9 Regulates Sperm Motility
inferredcites →https://doi.org/10.1016/j.celrep.2018.08.016openalex-snapshot
Asymmetrically Positioned Flagellar Control Units Regulate Human Sperm Rotation
inferredcites →https://doi.org/10.1016/j.cub.2013.02.007openalex-snapshot
Rheotaxis Guides Mammalian Sperm
inferredcites →https://doi.org/10.1016/j.mce.2009.02.006openalex-snapshot
Nongenomic activation of spermatozoa by steroid hormones: Facts and fictions
inferredcites →https://doi.org/10.1016/j.tcb.2016.10.002openalex-snapshot
Signaling in Sperm: More Different than Similar
inferredcites →https://doi.org/10.1016/j.ydbio.2006.05.038openalex-snapshot
Soluble adenylyl cyclase (sAC) is indispensable for sperm function and fertilization
inferredcites →https://doi.org/10.1016/j.ydbio.2007.09.017openalex-snapshot
External Ca2+ acts upstream of adenylyl cyclase SACY in the bicarbonate signaled activation of sperm motility
inferredcites →https://doi.org/10.1016/s0022-5347(17)41225-0openalex-snapshot
Effects of Extracellular Ionized Calcium, Diltiazem and Camp on Motility of Human Spermatozoa
inferredcites →https://doi.org/10.1021/ja808334fopenalex-snapshot
Caged Progesterone: A New Tool for Studying Rapid Nongenomic Actions of Progesterone
inferredcites →https://doi.org/10.1038/35098027openalex-snapshot
A sperm ion channel required for sperm motility and male fertility
inferredcites →https://doi.org/10.1038/ejhg.2010.108openalex-snapshot
Genetic male infertility and mutation of CATSPER ion channels
inferredcites →https://doi.org/10.1038/emboj.2012.30openalex-snapshot
The CatSper channel: a polymodal chemosensor in human sperm
inferredcites →https://doi.org/10.1038/ki.2011.95openalex-snapshot
Intracellular cAMP signaling by soluble adenylyl cyclase
inferredcites →https://doi.org/10.1038/nature04417openalex-snapshot
Whole-cell patch-clamp measurements of spermatozoa reveal an alkaline-activated Ca2+ channel
inferredcites →https://doi.org/10.1038/nature09767openalex-snapshot
Progesterone activates the principal Ca2+ channel of human sperm
inferredcites →https://doi.org/10.1038/nature09769openalex-snapshot
The CatSper channel mediates progesterone-induced Ca2+ influx in human sperm
inferredcites →https://doi.org/10.1038/ncb915openalex-snapshot
The signal flow and motor response controling chemotaxis of sea urchin sperm
inferredcites →https://doi.org/10.1038/ncomms1153openalex-snapshot
A novel gene required for male fertility and functional CATSPER channel formation in spermatozoa
inferredcites →https://doi.org/10.1038/ncomms8985openalex-snapshot
Sperm navigation along helical paths in 3D chemoattractant landscapes
inferredcites →https://doi.org/10.1038/ncomms9703openalex-snapshot
Two-dimensional slither swimming of sperm within a micrometre of a surface
inferredcites →https://doi.org/10.1038/nmeth.1274openalex-snapshot
Whole-cell 3D STORM reveals interactions between cellular structures with nanometer-scale resolution
inferredcites →https://doi.org/10.1038/srep23553openalex-snapshot
Human sperm rheotaxis: a passive physical process
inferredcites →https://doi.org/10.1039/c3lc51297eopenalex-snapshot
Cooperative roles of biological flow and surface topography in guiding sperm migration revealed by a microfluidic model
inferredcites →https://doi.org/10.1039/c4ib00196fopenalex-snapshot
Characterization of rheotaxis of bull sperm using microfluidics
inferredcites →https://doi.org/10.1042/bj20021560openalex-snapshot
Encoding of progesterone stimulus intensity by intracellular [Ca2+] ([Ca2+]i) in human spermatozoa
inferredcites →https://doi.org/10.1073/pnas.0400050101openalex-snapshot
Mice deficient for soluble adenylyl cyclase are infertile because of a severe sperm-motility defect
inferredcites →https://doi.org/10.1073/pnas.1216588110openalex-snapshot
Disruption of the principal, progesterone-activated sperm Ca 2+ channel in a CatSper2-deficient infertile patient
inferredcites →https://doi.org/10.1073/pnas.1515159112openalex-snapshot
Bimodal rheotactic behavior reflects flagellar beat asymmetry in human sperm cells
inferredcites →https://doi.org/10.1073/pnas.1700367114openalex-snapshot
Regulation of the sperm calcium channel CatSper by endogenous steroids and plant triterpenoids
inferredcites →https://doi.org/10.1073/pnas.1717929115openalex-snapshot
Action of steroids and plant triterpenoids on CatSper Ca 2+ channels in human sperm
inferredcites →https://doi.org/10.1073/pnas.221454998openalex-snapshot
A voltage-gated ion channel expressed specifically in spermatozoa
inferredcites →https://doi.org/10.1073/pnas.95.6.3008openalex-snapshot
A new prostaglandin E receptor mediates calcium influx and acrosome reaction in human spermatozoa
inferredcites →https://doi.org/10.1074/jbc.m701083200openalex-snapshot
CatSperβ, a Novel Transmembrane Protein in the CatSper Channel Complex
inferredcites →https://doi.org/10.1093/humrep/den265openalex-snapshot
The sperm chemoattractant secreted from human cumulus cells is progesterone
inferredcites →https://doi.org/10.1093/humrep/der237openalex-snapshot
Sodium influx induced by external calcium chelation decreases human sperm motility
inferredcites →https://doi.org/10.1093/humrep/des467openalex-snapshot
The clinical significance of calcium-signalling pathways mediating human sperm hyperactivation
inferredcites →https://doi.org/10.1093/humrep/det454openalex-snapshot
The CatSper calcium channel in human sperm: relation with motility and involvement in progesterone-induced acrosome reaction
inferredcites →https://doi.org/10.1093/humrep/dev103openalex-snapshot
Quantification of CatSper1 expression in human spermatozoa and relation to functional parameters
inferredcites →https://doi.org/10.1093/humrep/dey275openalex-snapshot
Synergistic activation of CatSper Ca2+ channels in human sperm by oviductal ligands and endocrine disrupting chemicals
inferredcites →https://doi.org/10.1093/humrep/dez056openalex-snapshot
Rapid sperm capture: high-throughput flagellar waveform analysis
inferredcites →https://doi.org/10.1095/biolreprod.107.060186openalex-snapshot
Catsper3 and Catsper4 Are Essential for Sperm Hyperactivated Motility and Male Fertility in the Mouse1
inferredcites →https://doi.org/10.1095/biolreprod.109.077107openalex-snapshot
A Novel, Single, Transmembrane Protein CATSPERG Is Associated with CATSPER1 Channel Protein1
inferredcites →https://doi.org/10.1095/biolreprod.113.111708openalex-snapshot
CatSper and the Relationship of Hyperactivated Motility to Intracellular Calcium and pH Kinetics in Equine Sperm1
inferredcites →https://doi.org/10.1103/physrevlett.114.108102openalex-snapshot
Emergence of Upstream Swimming via a Hydrodynamic Transition
inferredcites →https://doi.org/10.1111/bph.14355openalex-snapshot
A novel cross‐species inhibitor to study the function of CatSper Ca2+ channels in sperm
inferredcites →https://doi.org/10.1113/jp273189openalex-snapshot
Post‐translational cleavage of Hv1 in human sperm tunes pH‐ and voltage‐dependent gating
inferredcites →https://doi.org/10.1126/science.aad6887openalex-snapshot
Unconventional endocannabinoid signaling governs sperm activation via the sex hormone progesterone
inferredcites →https://doi.org/10.1136/jmg.2006.045765openalex-snapshot
Sensorineural deafness and male infertility: a contiguous gene deletion syndrome
inferredcites →https://doi.org/10.1186/s12915-014-0067-3openalex-snapshot
Episodic rolling and transient attachments create diversity in sperm swimming behavior
inferredcites →https://doi.org/10.1364/ol.11.000288openalex-snapshot
Observation of a single-beam gradient force optical trap for dielectric particles
inferredcites →https://doi.org/10.1371/journal.pone.0019426openalex-snapshot
Copy Number Variants in Patients with Severe Oligozoospermia and Sertoli-Cell-Only Syndrome
inferredcites →https://doi.org/10.1371/journal.pone.0199678openalex-snapshot
Four-dimensional analysis by high-speed holographic imaging reveals a chiral memory of sperm flagella
inferredcites →https://doi.org/10.1387/ijdb.072554bnopenalex-snapshot
Ion channels that control fertility in mammalian spermatozoa
inferredcites →https://doi.org/10.15252/embj.201489376openalex-snapshot
The CatSper channel controls chemosensation in sea urchin sperm
inferredcites →https://doi.org/10.15252/embr.201438869openalex-snapshot
Direct action of endocrine disrupting chemicals on human sperm
inferredcites →https://doi.org/10.1530/jrf.0.0730441openalex-snapshot
Relationship between the movement characteristics of human spermatozoa and their ability to penetrate cervical mucus and zona-free hamster oocytes
inferredcites →https://doi.org/10.2741/3105openalex-snapshot
Ca2+ signalling in the control of motility and guidance in mammalian sperm
inferredcites →https://doi.org/10.7554/elife.02403openalex-snapshot
Rheotaxis facilitates upstream navigation of mammalian sperm cells
inferredcites →https://doi.org/10.7554/elife.07624openalex-snapshot
A K+-selective CNG channel orchestrates Ca2+ signalling in zebrafish sperm
inferredcites →https://doi.org/10.7554/elife.23082openalex-snapshot
CatSperζ regulates the structural continuity of sperm Ca2+ signaling domains and is required for normal fertility

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.12688/openreseurope.16671.1zenodo-depositor-declared
Lab-on-chip (LoC) application for quality sperm selection: An undelivered promise?
inferred← citeshttps://doi.org/10.1007/978-3-031-08881-0_23openalex-snapshot
Voltage-Dependent Calcium Channels (CaVs) and CatSper in Spermatogenic and Sperm Cells
inferred← citeshttps://doi.org/10.1007/978-3-662-61901-8_3openalex-snapshot
Physiologie der Spermienreifung und Fertilisierung
inferred← citeshttps://doi.org/10.1007/s00232-024-00316-1openalex-snapshot
Sperm-Specific CatSper is Not Conserved in All Vertebrates and May Not be the Only Progesterone-Responsive Ion Channel Present in Sperm
inferred← citeshttps://doi.org/10.1007/s00521-022-07390-3openalex-snapshot
A hybrid IMM-JPDAF algorithm for tracking multiple sperm targets and motility analysis
inferred← citeshttps://doi.org/10.1007/s44369-026-00005-7openalex-snapshot
Rheotaxis of sperm cells: mechanism and applications in microfluidic separation
inferred← citeshttps://doi.org/10.1016/j.apm.2026.116909openalex-snapshot
A microtubule-sliding–based sperm model for near-wall swimming dynamics
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.110226openalex-snapshot
C2cd6-encoded CatSperτ targets sperm calcium channel to Ca2+ signaling domains in the flagellar membrane
inferred← citeshttps://doi.org/10.1016/j.mce.2020.110951openalex-snapshot
CatSper: The complex main gate of calcium entry in mammalian spermatozoa
inferred← citeshttps://doi.org/10.1016/j.mce.2020.110952openalex-snapshot
Progesterone, spermatozoa and reproduction: An updated review
inferred← citeshttps://doi.org/10.1016/j.mce.2020.110953openalex-snapshot
Ca2+ signaling in mammalian spermatozoa
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2022.01.011openalex-snapshot
An ex-vivo assessment of differential sperm transport in the female reproductive tract between high and low fertility bulls
inferred← citeshttps://doi.org/10.1016/j.trac.2023.117255openalex-snapshot
Single-molecule detection-based super-resolution imaging in single-cell analysis: Inspiring progress and future prospects
inferred← citeshttps://doi.org/10.1016/j.xcrp.2023.101646openalex-snapshot
The cooperative impact of flow and viscosity on sperm flagellar energetics in biomimetic environments
inferred← citeshttps://doi.org/10.1021/acsptsci.6c00091openalex-snapshot
Off-Target Activation of CatSper Limits the Utility of a Novel Small Molecule Slo3 Inhibitor and its Derivatives in Human Sperm
inferred← citeshttps://doi.org/10.1038/s41467-022-31050-8openalex-snapshot
3D structure and in situ arrangements of CatSper channel in the sperm flagellum
inferred← citeshttps://doi.org/10.1038/s41467-023-40855-0openalex-snapshot
Control of intracellular pH and bicarbonate by CO2 diffusion into human sperm
inferred← citeshttps://doi.org/10.1038/s41567-025-02783-2openalex-snapshot
Twist–torsion coupling in beating axonemes
inferred← citeshttps://doi.org/10.1038/s41585-020-00390-9openalex-snapshot
Sperm ion channels and transporters in male fertility and infertility
inferred← citeshttps://doi.org/10.1038/s41585-021-00530-9openalex-snapshot
Simulating nature in sperm selection for assisted reproduction
inferred← citeshttps://doi.org/10.1038/s41598-021-88568-yopenalex-snapshot
Artificial insemination and parthenogenesis in the whitespotted bamboo shark Chiloscyllium plagiosum
inferred← citeshttps://doi.org/10.1038/s42003-025-08358-4openalex-snapshot
Sperm navigation in humans: a concerted action of multiple means
inferred← citeshttps://doi.org/10.1039/d2lc00150kopenalex-snapshot
Rheotaxis quality index: a new parameter that reveals male mammalian in vivo fertility and low sperm DNA fragmentation
inferred← citeshttps://doi.org/10.1071/rd26043openalex-snapshot
Assisted reproductive technologies on-chip: the application of microfluidics and optics to sperm assessment and sorting
inferred← citeshttps://doi.org/10.1074/jbc.ra120.013218openalex-snapshot
The Ca2+ channel CatSper is not activated by cAMP/PKA signaling but directly affected by chemicals used to probe the action of cAMP and PKA
inferred← citeshttps://doi.org/10.1080/19768354.2024.2345647openalex-snapshot
Ca 2+ homeostasis and male fertility: a target for a new male contraceptive system
inferred← citeshttps://doi.org/10.1080/19942060.2021.2008500openalex-snapshot
Hydrodynamic behaviors of self-propelled sperms in confined spaces
inferred← citeshttps://doi.org/10.1093/biolre/ioaf268openalex-snapshot
Thermal modulation of CatSper activity regulates hyperactivated motility in human sperm
inferred← citeshttps://doi.org/10.1093/humrep/deab190openalex-snapshot
The antidepressant Sertraline inhibits CatSper Ca2+ channels in human sperm
inferred← citeshttps://doi.org/10.1093/humrep/deaf020openalex-snapshot
The major phytocannabinoids, delta-9-tetrahydrocannabinol (THC) and cannabidiol (CBD), affect the function of CatSper calcium channels in human sperm
inferred← citeshttps://doi.org/10.1093/molehr/gaac027openalex-snapshot
Thermotaxis of mammalian sperm
inferred← citeshttps://doi.org/10.1101/2025.09.14.675619openalex-snapshot
Membrane potential and feedback dynamics regulate CatSper-mediated progesterone signaling in human sperm
inferred← citeshttps://doi.org/10.1111/bph.70009openalex-snapshot
Chemosensory signalling in human sperm is controlled by Ca2+ influx via CatSper and Ca2+ clearance via plasma membrane Ca2+ ATPases
inferred← citeshttps://doi.org/10.1140/epje/s10189-021-00050-9openalex-snapshot
Micromotor-mediated sperm constrictions for improved swimming performance
inferred← citeshttps://doi.org/10.1140/epje/s10189-021-00076-zopenalex-snapshot
Reconstruction of the three-dimensional beat pattern underlying swimming behaviors of sperm
inferred← citeshttps://doi.org/10.1146/annurev-animal-021022-040629openalex-snapshot
Sperm in the Mammalian Female Reproductive Tract: Surfing Through the Tract to Try to Beat the Odds
inferred← citeshttps://doi.org/10.1152/function.083.2025openalex-snapshot
The systems that transport ions and their impact on sperm function and male fertility
inferred← citeshttps://doi.org/10.1152/physiol.00028.2022openalex-snapshot
CatSper Calcium Channels: 20 Years On
inferred← citeshttps://doi.org/10.1172/jci173564openalex-snapshot
Human fertilization in vivo and in vitro requires the CatSper channel to initiate sperm hyperactivation
inferred← citeshttps://doi.org/10.1186/s12958-025-01476-yopenalex-snapshot
Colony-stimulating factor-1 as a potential therapeutic target in asthenozoospermia
inferred← citeshttps://doi.org/10.12688/f1000research.109279.1openalex-snapshot
Lupeol and pristimerin do not inhibit activation of the human sperm CatSper Ca(2+)-channel
inferred← citeshttps://doi.org/10.1364/boe.519258openalex-snapshot
Time and power dependence of laser-induced photodamage on human sperm revealed by longitudinal rolling measurement using optical tweezers
inferred← citeshttps://doi.org/10.1530/raf-21-0001openalex-snapshot
Behavioural switching during oscillations of intracellular Ca2+ concentration in free-swimming human sperm
inferred← citeshttps://doi.org/10.3389/fbioe.2022.1028857openalex-snapshot
Chirality and frequency measurement of longitudinal rolling of human sperm using optical trap
inferred← citeshttps://doi.org/10.3389/fcell.2021.699554openalex-snapshot
The Action of Reproductive Fluids and Contained Steroids, Prostaglandins, and Zn2+ on CatSper Ca2+ Channels in Human Sperm
inferred← citeshttps://doi.org/10.3389/fcell.2023.1136537openalex-snapshot
CatSper mediates not only chemotactic behavior but also the motility of ascidian sperm
inferred← citeshttps://doi.org/10.3389/fcell.2023.1221578openalex-snapshot
The action of physiological and synthetic steroids on the calcium channel CatSper in human sperm
inferred← citeshttps://doi.org/10.3389/fcell.2024.1284988openalex-snapshot
Analysis of Ca2+-mediated sperm motility to evaluate the functional normality of the sperm-specific Ca2+ channel, CatSper
inferred← citeshttps://doi.org/10.3389/fendo.2020.00324openalex-snapshot
Bisphenol A Diglycidyl Ether (BADGE) and Bisphenol Analogs, but Not Bisphenol A (BPA), Activate the CatSper Ca2+ Channel in Human Sperm
inferred← citeshttps://doi.org/10.3390/cells10061297openalex-snapshot
Co-Adaptation of Physical Attributes of the Mammalian Female Reproductive Tract and Sperm to Facilitate Fertilization
inferred← citeshttps://doi.org/10.3390/ijms21062174openalex-snapshot
The Roles of NO and H2S in Sperm Biology: Recent Advances and New Perspectives
inferred← citeshttps://doi.org/10.3390/ijms22094306openalex-snapshot
Role and Modulation of TRPV1 in Mammalian Spermatozoa: An Updated Review
inferred← citeshttps://doi.org/10.3390/ijms23073926openalex-snapshot
Sperm Ion Transporters and Channels in Human Asthenozoospermia: Genetic Etiology, Lessons from Animal Models, and Clinical Perspectives
inferred← citeshttps://doi.org/10.3390/ijms231810607openalex-snapshot
cAMP and the Fibrous Sheath Protein CABYR (Ca2+-Binding Tyrosine-Phosphorylation-Regulated Protein) Is Required for 4D Sperm Movement
inferred← citeshttps://doi.org/10.5187/jast.2023.e133openalex-snapshot
Sperm hyperactivation and the CatSper channel: current understanding and future contribution of domestic animals
inferred← citeshttps://doi.org/10.7554/elife.68693openalex-snapshot
Rolling controls sperm navigation in response to the dynamic rheological properties of the environment
inferred← citeshttps://doi.org/10.7717/peerj.18429openalex-snapshot
The regulation role of calcium channels in mammalian sperm function: a narrative review with a focus on humans and mice
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