Rapid non-genomic actions of progesterone stimulate Ca2+ influx and the acrosome reaction in human sperm.

Abstract:

:This review summarizes some recent findings in human sperm which show that progesterone and 17 alpha hydroxyprogesterone are able rapidly (within seconds) to elevate [Ca2+]i and elicit the acrosome reaction (AR) via a non-genomic cell surface receptor. Progesterone promotes a transient elevation in [Ca2+]i which is blocked by extracellular La3+ and Ni2+ and removal of extracellular Ca2+ following chelation with EGTA. Some studies suggest that polyamines, trypsin-like proteases, and progesterone receptor aggregation are involved in progesterone-induced Ca2+ influx and AR. The receptor is not stimulated by the potent synthetic progestigins (e.g. promegestone, norethynodrel, megestrol acetate, cyproterone acetate) and is weakly antagonized by the genomic anti-progestins RU 486 and ZK 98.299. The sedative-hypnotic 3 alpha hydroxyl A-ring reduced pregnane steroids, which are powerful activators of the GABAA Cl- channel, are weak activators of Ca2+ influx and the AR. These data suggest that human sperm have a cell surface steroid receptor which is unlike the genomic progesterone receptor and the GABAA Cl- channel steroid receptor.

journal_name

Cell Signal

journal_title

Cellular signalling

authors

Blackmore PF

doi

10.1016/0898-6568(93)90048-q

subject

Has Abstract

pub_date

1993-09-01 00:00:00

pages

531-8

issue

5

eissn

0898-6568

issn

1873-3913

pii

0898-6568(93)90048-Q

journal_volume

5

pub_type

杂志文章,评审
  • Structural determinants of LL5beta subcellular localisation and association with filamin C.

    abstract::PI3K signalling pathways link cell surface receptors to the control of several intracellular functions including cell growth, survival and movement. Filamins are important regulators of cortical actin structure and function. LL5beta is a filamin binding protein that is an effector of the PI3K signalling pathway. We de...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2006.10.007

    authors: Paranavitane V,Stephens LR,Hawkins PT

    更新日期:2007-04-01 00:00:00

  • Lysophosphatidic acid-induced arterial wall remodeling: requirement of PPARgamma but not LPA1 or LPA2 GPCR.

    abstract::Lysophosphatidic acid (LPA) and its ether analog alkyl-glycerophosphate (AGP) elicit arterial wall remodeling when applied intralumenally into the uninjured carotid artery. LPA is the ligand of eight GPCRs and the peroxisome proliferator-activated receptor gamma (PPARgamma). We pursued a gene knockout strategy to iden...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2009.08.003

    authors: Cheng Y,Makarova N,Tsukahara R,Guo H,Shuyu E,Farrar P,Balazs L,Zhang C,Tigyi G

    更新日期:2009-12-01 00:00:00

  • Genomic analysis of G protein gamma subunits in human and mouse - the relationship between conserved gene structure and G protein betagamma dimer formation.

    abstract::Analysis of the genomic sequences, cDNAs and expressed sequence tags (ESTs) in human and mouse for the 12 genes of the gamma subunits of the heterotrimeric G proteins has allowed us to identify the common versus unique elements of the organization and expression of the members of this important gene family. All of the...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2005.04.011

    authors: Yang W,Hildebrandt JD

    更新日期:2006-02-01 00:00:00

  • Insulin-induced cell division is controlled by the adaptor Grb14 in a Chfr-dependent manner.

    abstract::Beyond its key role in the control of energy metabolism, insulin is also an important regulator of cell division and neoplasia. However, the molecular events involved in insulin-driven cell proliferation are not fully elucidated. Here, we show that the ubiquitin ligase Chfr, a checkpoint protein involved in G2/M trans...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2015.01.003

    authors: Perdereau D,Cailliau K,Browaeys-Poly E,Lescuyer A,Carré N,Benhamed F,Goenaga D,Burnol AF

    更新日期:2015-04-01 00:00:00

  • Molecular interactions of SHP1 and SHP2 in IL-3-signalling.

    abstract::SHP1 and SHP2 tyrosine phosphatases have both been implicated in signalling pathways downstream of the interleukin-3 (IL-3) receptor. We have investigated the co-association of SHP1 and SHP2 with tyrosine-phosphorylated proteins in IL-3-dependent BaF/3 cells. We demonstrate that both SHP1 and SHP2 associate with Aic2A...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/s0898-6568(01)00241-8

    authors: Wheadon H,Paling NR,Welham MJ

    更新日期:2002-03-01 00:00:00

  • Angiotensin II induces nephrin dephosphorylation and podocyte injury: role of caveolin-1.

    abstract::Nephrin, an important structural and signal molecule of podocyte slit-diaphragm (SD), has been suggested to contribute to the angiotensin II (Ang II)-induced podocyte injury. Caveolin-1 has been demonstrated to play a crucial role in signaling transduction. In the present study, we evaluated the role of caveolin-1 in ...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2011.09.022

    authors: Ren Z,Liang W,Chen C,Yang H,Singhal PC,Ding G

    更新日期:2012-02-01 00:00:00

  • Arf GAPs: multifunctional proteins that regulate membrane traffic and actin remodelling.

    abstract::The ADP-ribosylation factor (Arf) Arf GTPase-activating proteins (GAPs) are a family of proteins that induce hydrolysis of GTP bound to Arf. A conserved domain containing a zinc finger motif mediates catalysis. The substrate, Arf.GTP, affects membrane trafficking and actin remodelling. Consistent with activity as an A...

    journal_title:Cellular signalling

    pub_type: 杂志文章,评审

    doi:10.1016/j.cellsig.2003.09.012

    authors: Randazzo PA,Hirsch DS

    更新日期:2004-04-01 00:00:00

  • Physiological levels of PTEN control the size of the cellular Ins(1,3,4,5,6)P(5) pool.

    abstract::To understand how a signaling molecule's activities are regulated, we need insight into the processes controlling the dynamic balance between its synthesis and degradation. For the Ins(1,3,4,5,6)P5 signal, this information is woefully inadequate. For example, the only known cytosolic enzyme with the capacity to degrad...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2005.05.017

    authors: Deleu S,Choi K,Pesesse X,Cho J,Sulis ML,Parsons R,Shears SB

    更新日期:2006-04-01 00:00:00

  • Oncogenic RAC1 and NRAS drive resistance to endoplasmic reticulum stress through MEK/ERK signalling.

    abstract::Cancer cells are able to survive under conditions that cause endoplasmic reticulum stress (ER-stress), and can adapt to this stress by upregulating cell-survival signalling pathways and down-regulating apoptotic pathways. The cellular response to ER-stress is controlled by the unfolded protein response (UPR). Small Rh...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2018.01.004

    authors: Bright MD,Clarke PA,Workman P,Davies FE

    更新日期:2018-04-01 00:00:00

  • Proteasome inhibitor-I enhances tunicamycin-induced chemosensitization of prostate cancer cells through regulation of NF-κB and CHOP expression.

    abstract::Although endoplasmic reticulum (ER) stress induction by some anticancer drugs can lead to apoptotic death of cancer cells, combination therapy with other chemicals would be much more efficient. It has been reported that proteasome inhibitors could induce cancer cell death through ER-stress. Our study, however, showed ...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2011.01.010

    authors: Huong PT,Moon DO,Kim SO,Kim KE,Jeong SJ,Lee KW,Lee KS,Jang JH,Erikson RL,Ahn JS,Kim BY

    更新日期:2011-05-01 00:00:00

  • Is the glycogen synthase analogue C1-peptide a suitable fluorescent substrate for routine measurements of protein kinase C?

    abstract::We have compared a new commercially available non-radioactive protein kinase C (PKC) activity assay based on the fluorescent [A9,10K11]glycogen synthase1-11 analogue C1-peptide with a classical radioactive assay based on myelin basic protein4-14 (MBP4-14) and other substrates. The C1-peptide had lower affinity for PKC...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/0898-6568(95)00029-o

    authors: Erdbrügger W,Strohm P,Michel MC

    更新日期:1995-08-01 00:00:00

  • GATA3-driven expression of miR-503 inhibits prostate cancer progression by repressing ZNF217 expression.

    abstract::Although increasing evidence demonstrated that deregulation of mircoRNA-503 (miRNA-503) contributes to tumorigenesis, little is known about the biological role and intrinsic regulatory mechanisms of miR-503 in prostate cancer (PCa). In present study, we found that miR-503 was significantly downregulated in advanced PC...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2016.06.002

    authors: Jiang X,Chen Y,Du E,Yang K,Zhang Z,Qi S,Xu Y

    更新日期:2016-09-01 00:00:00

  • The interaction of dystrophin with beta-dystroglycan is regulated by tyrosine phosphorylation.

    abstract::Dystrophin and the dystrophin-associated protein complex (DAPC) have recently been implicated in cell signalling events. These proteins are ideally placed to transduce signals from the extracellular matrix (ECM) to the cytoskeleton. Here we show that beta-dystroglycan is tyrosine-phosphorylated in C2/C4 mouse myotubes...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/s0898-6568(01)00188-7

    authors: Ilsley JL,Sudol M,Winder SJ

    更新日期:2001-09-01 00:00:00

  • Upregulation of sestrin 2 expression via JNK pathway activation contributes to autophagy induction in cancer cells.

    abstract::JNK signaling functions to induce defense mechanisms that protect organisms against a variety of different situations. The sestrin 2 gene, a p53-regulated member of the sestrins family, which lead to AMPK-dependent inhibition of TOR signaling, emerges as a novel player in autophagy induction. However, the relationship...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2012.09.004

    authors: Zhang XY,Wu XQ,Deng R,Sun T,Feng GK,Zhu XF

    更新日期:2013-01-01 00:00:00

  • Lysophosphatidic acid induces integrin β6 expression in human oral squamous cell carcinomas cells via LPAR1 coupling to Gαi and downstream SMAD3 and ETS-1 activation.

    abstract::Integrin β6 (ITGB6), an epithelial-specific integrin, is upregulated in oral squamous cell carcinomas (OSCC) and is associated with progression and metastasis of OSCC. Lysophosphatidic acid (LPA), an important bioactive phospholipid present in saliva, has also been related to OSCC cell migration and invasiveness. LPA ...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2019.04.008

    authors: Xu M,Yin H,Cai Y,Huang W,Ji Q,Liu F,Shi S,Deng X

    更新日期:2019-08-01 00:00:00

  • A novel role for Gq alpha in alpha-thrombin-mediated mitogenic signalling pathways.

    abstract::alpha-Thrombin activates several G-proteins including members of the Gq, Gi, and G12/13 families, although the physiological importance of these proteins is still not completely understood. We specifically investigated the role of Gq alpha in modulating alpha-thrombin-induced mitogenesis. In Gqa1 cells, a stable cell ...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/s0898-6568(01)00279-0

    authors: Gardner A,Phillips-Mason PJ,Raben DM,Baldassare JJ

    更新日期:2002-06-01 00:00:00

  • Interleukin-17A stimulates cardiac fibroblast proliferation and migration via negative regulation of the dual-specificity phosphatase MKP-1/DUSP-1.

    abstract::The dual-specificity mitogen-activated protein kinase (MAPK) phosphatase-1 (MKP-1) inactivates MAP kinases by dephosphorylation. Here we show that the proinflammatory cytokine interleukin (IL)-17A induces adult mouse primary cardiac fibroblast (CF) proliferation and migration via IL-17 receptor A//IL-17 receptor C-dep...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2011.10.010

    authors: Valente AJ,Yoshida T,Gardner JD,Somanna N,Delafontaine P,Chandrasekar B

    更新日期:2012-02-01 00:00:00

  • Activation of c-Jun N-terminal kinase 1 (JNK-1) after amino acid deficiency in HeLa cells.

    abstract::Long-term amino acid starvation represents a form of metabolic stress which stimulates gene expression. Here we report that depriving HeLa cells for any one of a series of amino acids activates c-Jun N-terminal kinase-1 (JNK-1). In contrast, the other mitogen-activated protein kinases (MAPKs) ERK-1 and, to a lesser ex...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/s0898-6568(01)00159-0

    authors: Aubel C,Dehez S,Chabanon H,Seva C,Ferrara M,Brachet P

    更新日期:2001-06-01 00:00:00

  • Phosphodiesterase 4 in inflammatory diseases: Effects of apremilast in psoriatic blood and in dermal myofibroblasts through the PDE4/CD271 complex.

    abstract::Phosphodiesterases 4 (PDE4) act as proinflammatory enzymes via degradation of cAMP, whereas PDE4 inhibitors play an anti-inflammatory role in vitro and in vivo. In particular, apremilast has been recently approved for the treatment of psoriasis and psoriatic arthritis. However, little is known on the expression patter...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2016.01.007

    authors: Schafer PH,Truzzi F,Parton A,Wu L,Kosek J,Zhang LH,Horan G,Saltari A,Quadri M,Lotti R,Marconi A,Pincelli C

    更新日期:2016-07-01 00:00:00

  • Illumina-microarray analysis of mycophenolic acid-induced cell death in an insulin-producing cell line and primary rat islet cells: new insights into apoptotic pathways involved.

    abstract::Mycophenolic acid (MPA), widely used to prevent organ transplant rejection, may induce toxicity and impair function in beta-cells. Mechanisms of MPA-induced cell death have not been fully explored. In this study, we examined gene expression patterns in INS-1E cells and isolated primary rat islets following MPA treatme...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2010.07.005

    authors: Park YJ,Ahn HJ,Kim YS,Cho Y,Joo DJ,Ju MK

    更新日期:2010-11-01 00:00:00

  • Cycloheximide-induced cPLA(2) activation is via the MKP-1 down-regulation and ERK activation.

    abstract::Extracellular signal-regulated kinase (ERK)-dependent phosphorylation is an important regulator for cytosolic phospholipase A(2) (cPLA(2)). In this study, we found that the protein synthesis inhibitor cycloheximide can potentiate thapsigargin-induced arachidonic acid (AA) release concomitant with ERK phosphorylation f...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/s0898-6568(00)00090-5

    authors: Lin WW,Hsu YW

    更新日期:2000-07-01 00:00:00

  • p130Cas: a key signalling node in health and disease.

    abstract::p130Cas/breast cancer anti-oestrogen resistance 1 (BCAR1) is a member of the Cas (Crk-associated substrate) family of adaptor proteins, which have emerged as key signalling nodes capable of interactions with multiple proteins, with important regulatory roles in normal and pathological cell function. The Cas family of ...

    journal_title:Cellular signalling

    pub_type: 杂志文章,评审

    doi:10.1016/j.cellsig.2012.12.019

    authors: Barrett A,Pellet-Many C,Zachary IC,Evans IM,Frankel P

    更新日期:2013-04-01 00:00:00

  • Loss of Raf-1-binding activity of v-Ha-Ras by the deletion of amino acid residues 64-72 and 143-151.

    abstract::In order to elucidate the molecular events in signal transduction, examination of the interaction between Ras and Raf-1 seems crucial. Many Raf-1 mutants have been investigated in terms of their binding activities to Ras, where only a few Ras mutants have been examined thus far. We have investigated the Raf-1-binding ...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/0898-6568(96)00078-2

    authors: Hiwasa T,Kasama M,Nakadai T,Sawada T,Sakiyama S

    更新日期:1996-08-01 00:00:00

  • Granzyme B induction signalling pathway in acute myeloid leukemia cell lines stimulated by tumor necrosis factor alpha and Fas ligand.

    abstract::Acute myeloid leukemia (AML) cell lines treated by genotoxic agents or by Tumor Necrosis Factor alpha (TNFalpha) acquire potent cytotoxicity towards myeloid cells through activation of granzyme B (GrB)/perforin (PFN) system. Here we first extend this observation to another death receptor activator, Fas Ligand (FasL). ...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2006.12.005

    authors: Guilloton F,Jean C,de Thonel A,Laurent G,Quillet-Mary A

    更新日期:2007-06-01 00:00:00

  • Adenosine A1 receptors inhibit both adenylate cyclase activity and TRH-activated Ca2+ channels by a pertussis toxin-sensitive mechanism in GH3 cells.

    abstract::The present study has examined the effects of adenosine A1 receptors on second messenger processes in GH3 cells. A1 receptors are present which are shown to inhibit adenylate cyclase in a GTP-requiring manner. Hormone (VIP) stimulation is also absolutely required for the observation of inhibition. Adenosine A1 recepto...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/0898-6568(89)90023-5

    authors: Cooper DM,Caldwell KK,Boyajian CL,Petcoff DW,Schlegel W

    更新日期:1989-01-01 00:00:00

  • Interaction of PLD1b with actin in antigen-stimulated mast cells.

    abstract::Phosphatidic acid, the product of phospholipase D catalysed phosphatidylcholine hydrolysis is an important signalling molecule that has been implicated in regulation of actin cytoskeleton remodelling and secretion from mast cells. We show that human PLD1b (hPLD1b) is an actin-binding protein and the N-terminus is pred...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2006.07.016

    authors: Farquhar MJ,Powner DJ,Levine BA,Wright MH,Ladds G,Hodgkin MN

    更新日期:2007-02-01 00:00:00

  • 5-Hydroxytryptamine-induced phosphoinositide hydrolysis and Ca2+ mobilisation in canine cultured aorta smooth muscle cells.

    abstract::The effect of 5-hydroxytryptamine (5-HT) on phospholipase C (PLC)-mediated phosphoinositide (PI) hydrolysis and intracellular Ca2+ ([Ca2+]i) changes was investigated in canine cultured aorta smooth muscle cells (ASMCs). 5-HT-stimulated inositol phosphate (IP) accumulation was time and concentration dependent with a ha...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/s0898-6568(99)00010-8

    authors: Chiu CT,Tsao HL,Fan LW,Wang CC,Chien CS,Yang CM

    更新日期:1999-05-01 00:00:00

  • Human colon carcinoma cell-line HCT116 transfected by antisense cDNA as a tool to study the Ku86 involvement in cell proliferation.

    abstract::In this work, we used colon carcinoma cell-line HCT116 to study the involvement of the 86-kDa subunit (Ku86) of DNA-protein kinase (DNA-PK) in human tumoural cell proliferation. We transfected these cells with a 639-bp cDNA encoding a Ku86 portion inserted into pcDNA3.1 vector in the antisense orientation. After selec...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/s0898-6568(00)00126-1

    authors: Sadji Z,Le Romancer M,Lewin MJ,Reyl-Desmars F

    更新日期:2000-12-01 00:00:00

  • Sec8 modulates TGF-β induced EMT by controlling N-cadherin via regulation of Smad3/4.

    abstract::Sec8 is one of the subunits of the exocyst, which is an evolutionarily conserved complex of eight proteins, comprising Sec3 (EXOC1), Sec5 (EXOC2), Sec6 (EXOC3), Sec8 (EXOC4), Sec10 (EXOC5), Sec15 (EXOC6), Exo70 (EXOC7), and Exo84 (EXOC8) subunits. Sec8 knockout mice embryos initiate gastrulation but are unable to prog...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2016.10.007

    authors: Tanaka T,Goto K,Iino M

    更新日期:2017-01-01 00:00:00

  • Gbetagamma subunit combinations differentially modulate receptor and effector coupling in vivo.

    abstract::In vitro, little specificity is seen for modulation of effectors by different combinations of Gbetagamma subunits from heterotrimeric G proteins. Here, we demonstrate that the coupling of specific combinations of Gbetagamma subunits to different receptors leads to a differential ability to modulate effectors in vivo. ...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/s0898-6568(00)00118-2

    authors: Robillard L,Ethier N,Lachance M,Hébert TE

    更新日期:2000-10-01 00:00:00