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Cdc42 activity is essential for the interplay between cAMP/PKA pathway and CatSper function

https://doi.org/10.1101/2020.08.24.264739

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

inferredcites →https://doi.org/10.1002/jcp.24873openalex-snapshot

Biphasic Role of Calcium in Mouse Sperm Capacitation Signaling Pathways

inferredcites →https://doi.org/10.1002/jcp.26883openalex-snapshot

Only a subpopulation of mouse sperm displays a rapid increase in intracellular calcium during capacitation

inferredcites →https://doi.org/10.1002/mrd.20192openalex-snapshot

Actin polymerization in the equatorial and postacrosomal regions of guinea pig spermatozoa during the acrosome reaction is regulated by G proteins

inferredcites →https://doi.org/10.1016/0014-5793(95)00962-9openalex-snapshot

Mouse sperm membrane potential: changes induced by Ca2+

inferredcites →https://doi.org/10.1016/j.ajhg.2009.03.004openalex-snapshot

Human Male Infertility Caused by Mutations in the CATSPER1 Channel Protein

inferredcites →https://doi.org/10.1016/j.ceca.2014.10.009openalex-snapshot

Flagellar ion channels of sperm: similarities and differences between species

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.chembiol.2006.02.009openalex-snapshot

Biochemical Suppression of Small-Molecule Inhibitors: A Strategy to Identify Inhibitor Targets and Signaling Pathway Components

inferredcites →https://doi.org/10.1016/j.cophys.2018.02.004openalex-snapshot

CatSper: a unique calcium channel of the sperm flagellum

inferredcites →https://doi.org/10.1016/j.ydbio.2015.07.008openalex-snapshot

PKA-dependent phosphorylation of LIMK1 and Cofilin is essential for mouse sperm acrosomal exocytosis

inferredcites →https://doi.org/10.1016/s0960-9822(00)00571-6openalex-snapshot

Cdc42 is required for PIP2-induced actin polymerization and early development but not for cell viability

inferredcites →https://doi.org/10.1017/s0967199406003790openalex-snapshot

Localization of the Rho GTPases and some Rho effector proteins in the sperm of several mammalian species

inferredcites →https://doi.org/10.1038/168697b0openalex-snapshot

Fertilizing Capacity of Spermatozoa deposited into the Fallopian Tubes

inferredcites →https://doi.org/10.1038/170326a0openalex-snapshot

The ‘Capacitation’ of the Mammalian Sperm

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/emboj.2012.30openalex-snapshot

The CatSper channel: a polymodal chemosensor in human sperm

inferredcites →https://doi.org/10.1038/emboj.2012.62openalex-snapshot

Sperm are promiscuous and CatSper is to blame…

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/ncb1047openalex-snapshot

Involvement of CFTR in uterine bicarbonate secretion and the fertilizing capacity of sperm

inferredcites →https://doi.org/10.1038/nchembio751openalex-snapshot

Secramine inhibits Cdc42-dependent functions in cells and Cdc42 activation in vitro

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/nrm1587openalex-snapshot

GEF means go: turning on RHO GTPases with guanine nucleotide-exchange factors

inferredcites →https://doi.org/10.1038/nrm3153openalex-snapshot

The 'invisible hand': regulation of RHO GTPases by RHOGDIs

inferredcites →https://doi.org/10.1038/sj.ejhg.5200991openalex-snapshot

CATSPER2, a human autosomal nonsyndromic male infertility gene

inferredcites →https://doi.org/10.1038/srep17721openalex-snapshot

Superdiffusive motion of membrane-targeting C2 domains

inferredcites →https://doi.org/10.1038/srep33589openalex-snapshot

Transient exposure to calcium ionophore enables in vitro fertilization in sterile mouse models

inferredcites →https://doi.org/10.1042/bst20120103openalex-snapshot

Rho family GTPases

inferredcites →https://doi.org/10.1073/pnas.0610286104openalex-snapshot

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

inferredcites →https://doi.org/10.1073/pnas.0611296104openalex-snapshot

A sperm-specific Na + /H + exchanger (sNHE) is critical for expression and in vivo bicarbonate regulation of the soluble adenylyl cyclase (sAC)

inferredcites →https://doi.org/10.1073/pnas.1016325108openalex-snapshot

Ergodic and nonergodic processes coexist in the plasma membrane as observed by single-molecule tracking

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.2136654100openalex-snapshot

Hyperactivated sperm motility driven by CatSper2 is required for fertilization

inferredcites →https://doi.org/10.1073/pnas.221454998openalex-snapshot

A voltage-gated ion channel expressed specifically in spermatozoa

inferredcites →https://doi.org/10.1074/jbc.m008340200openalex-snapshot

Caveolin-1 Regulates Transforming Growth Factor (TGF)-β/SMAD Signaling through an Interaction with the TGF-β Type I Receptor

inferredcites →https://doi.org/10.1074/jbc.m011252200openalex-snapshot

Identification of Sperm-specific Proteins That Interact with A-kinase Anchoring Proteins in a Manner Similar to the Type II Regulatory Subunit of PKA

inferredcites →https://doi.org/10.1074/jbc.m114.607556openalex-snapshot

SLO3 K+ Channels Control Calcium Entry through CATSPER Channels in Sperm

inferredcites →https://doi.org/10.1074/jbc.m206284200openalex-snapshot

Involvement of a Na+/HCO 3− Cotransporter in Mouse Sperm Capacitation

inferredcites →https://doi.org/10.1074/jbc.m701083200openalex-snapshot

CatSperβ, a Novel Transmembrane Protein in the CatSper Channel Complex

inferredcites →https://doi.org/10.1074/jbc.ra117.001566openalex-snapshot

CatSper channels are regulated by protein kinase A

inferredcites →https://doi.org/10.1074/jbc.ra118.002286openalex-snapshot

Disruption of protein kinase A localization induces acrosomal exocytosis in capacitated mouse sperm

inferredcites →https://doi.org/10.1083/jcb.200704169openalex-snapshot

Positive feedback between Cdc42 activity and H+ efflux by the Na-H exchanger NHE1 for polarity of migrating cells

inferredcites →https://doi.org/10.1083/jcb.201412041openalex-snapshot

CRISP1 as a novel CatSper regulator that modulates sperm motility and orientation during fertilization

inferredcites →https://doi.org/10.1093/bioinformatics/btu202openalex-snapshot

ThunderSTORM: a comprehensive ImageJ plug-in for PALM and STORM data analysis and super-resolution imaging

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/molehr/gar044openalex-snapshot

Rediscovering sperm ion channels with the patch-clamp technique

inferredcites →https://doi.org/10.1093/molehr/gau029openalex-snapshot

Membrane hyperpolarization during human sperm capacitation

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/biolreprod46.5.779openalex-snapshot

Hyperactivated Sperm Progress in the Mouse Oviduct1

inferredcites →https://doi.org/10.1095/biolreprod53.6.1280openalex-snapshot

Sperm Motility Hyperactivation Facilitates Penetration of the Hamster Zona Pellucida1

inferredcites →https://doi.org/10.1126/science.1153529openalex-snapshot

Three-Dimensional Super-Resolution Imaging by Stochastic Optical Reconstruction Microscopy

inferredcites →https://doi.org/10.1126/science.aad0836openalex-snapshot

Sperm calcineurin inhibition prevents mouse fertility with implications for male contraceptive

inferredcites →https://doi.org/10.1126/science.aad6887openalex-snapshot

Unconventional endocannabinoid signaling governs sperm activation via the sex hormone progesterone

inferredcites →https://doi.org/10.1177/1087057109352240openalex-snapshot

Identification of a Small GTPase Inhibitor Using a High-Throughput Flow Cytometry Bead-Based Multiplex Assay

inferredcites →https://doi.org/10.1186/1477-7827-1-53openalex-snapshot

Identification of human and mouse CatSper3 and CatSper4 genes: Characterisation of a common interaction domain and evidence for expression in testis

inferredcites →https://doi.org/10.1242/dev.121.4.1139openalex-snapshot

Capacitation of mouse spermatozoa: II. Protein tyrosine phosphorylation and capacitation are regulated by a cAMP-dependent pathway

inferredcites →https://doi.org/10.1242/dev.136499openalex-snapshot

The tyrosine kinase FER is responsible for the capacitation-associated increase in tyrosine phosphorylation in murine sperm

inferredcites →https://doi.org/10.1242/jcs.093344openalex-snapshot

Flow cytometry analysis reveals a decrease in intracellular sodium during sperm capacitation

inferredcites →https://doi.org/10.1242/jcs.113.1.103openalex-snapshot

Ropporin, a sperm-specific binding protein of rhophilin, that is localized in the fibrous sheath of sperm flagella

inferredcites →https://doi.org/10.1242/jcs.215897openalex-snapshot

The actin cytoskeleton of the mouse sperm flagellum is organized in a helical structure

inferredcites →https://doi.org/10.1364/oe.20.004957openalex-snapshot

PSF shaping using adaptive optics for three-dimensional single-molecule super-resolution imaging and tracking

inferredcites →https://doi.org/10.1387/ijdb.072554bnopenalex-snapshot

Ion channels that control fertility in mammalian spermatozoa

inferredcites →https://doi.org/10.1530/rep-11-0433openalex-snapshot

The association between CDC42 and caveolin-1 is involved in the regulation of capacitation and acrosome reaction of guinea pig and mouse sperm

inferredcites →https://doi.org/10.2164/jandrol.109.009662openalex-snapshot

Functional Expression of Ropporin in Human Testis and Ejaculated Spermatozoa

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

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