2003
DOI: 10.1016/s0898-6568(03)00053-6
|View full text |Cite
|
Sign up to set email alerts
|

Regulation of phospholipase D by P2X7 receptors in submandibular ductal cells

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
37
0
2

Year Published

2009
2009
2013
2013

Publication Types

Select...
5
1

Relationship

1
5

Authors

Journals

citations
Cited by 27 publications
(41 citation statements)
references
References 50 publications
2
37
0
2
Order By: Relevance
“…The first mechanism involves a P2X7R-mediated activation of phospholipase D that facilitates maturation and fusion of the mycobacteria/ chlamydia-containing phagosomes with lysosomes [50]. As noted previously, P2X7R-dependent activation of phospholipase D and A 2 has been described in several cell types including macrophages [48,58,[61][62][63]. Although this P2X7R→PLD pathway clearly contributes to the phagosomal maturation and microbiocidal effects stimulated by extracellular ATP, additional purinergic receptors are involved given the differential microbiocidal actions of ATP versus BzATP [58].…”
Section: P2x7r Regulation Of Phagosome Maturation and Microbial Killingmentioning
confidence: 98%
“…The first mechanism involves a P2X7R-mediated activation of phospholipase D that facilitates maturation and fusion of the mycobacteria/ chlamydia-containing phagosomes with lysosomes [50]. As noted previously, P2X7R-dependent activation of phospholipase D and A 2 has been described in several cell types including macrophages [48,58,[61][62][63]. Although this P2X7R→PLD pathway clearly contributes to the phagosomal maturation and microbiocidal effects stimulated by extracellular ATP, additional purinergic receptors are involved given the differential microbiocidal actions of ATP versus BzATP [58].…”
Section: P2x7r Regulation Of Phagosome Maturation and Microbial Killingmentioning
confidence: 98%
“…Il est maintenant bien établi que les récepteurs P2X 7 régulent le métabolisme des phospholipides et activent les phospholipases A 2 et D (PLA 2 et PLD) [24,25]. Le méca-nisme de couplage entre le récepteur P2X 7 et l'activation de PLA 2 implique probablement une MAP kinase.…”
Section: Les Voies De Signalisation Couplées Aux Récepteurs P2x Des Gunclassified
“…Le méca-nisme de couplage entre le récepteur P2X 7 et l'activation de PLA 2 implique probablement une MAP kinase. Quant à l'activation de la PLD, elle dépend du niveau de calcium, ainsi que de la stimulation de la PLA 2 et de la protéine kinase C (PKC) [25,26]. L'activation des récepteurs P2X 7 augmente aussi la concentration de céramides dans les glandes sous-maxillaires de rat suite à l'activation d'une …”
Section: Les Voies De Signalisation Couplées Aux Récepteurs P2x Des Gunclassified
“…Moreover, the activation of PLD by P2X7R was partially dependent on calcium [32]. However, the use of calcium ionophores or the release of calcium stores by thapsigargin could not fully reproduce P2X7R signaling, and the involved signaling pathway was described as being associated with recruitment of different kinases, such as, PKC [35][36][37] or tyrosine kinase [35].…”
Section: P2x7r and The Lipid Metabolism Signaling Pathwaymentioning
confidence: 99%
“…Later, the activation of P2X7R was directly associated with several cellular pathways, including the following: caspase-1 activation [18] and IL-1β maturation [19]; shedding of membrane proteins [20]; recruitment and activation of protein kinases, such as, the mitogen-activated protein kinase [21], protein kinase C (PKC) [22], Src [23], and glycogen synthase kinase 3 [24]; recruitment and activation of phosphatases [15]; and membrane blebbing via the activity of ROCK [25] and the activation of epithelial membrane proteins [26]. Despite this wide assortment of functions, this review will focus on the ability of P2X7R to modulate lipid pathways through the activation of different enzymes, such as, phospholipase A 2 (PLA2) [27,28], phospholipase C (PLC) [29][30][31], phospholipase D (PLD) [32][33][34][35][36][37][38][39], and sphingomyelinases [27,36]. Additionally, it will discuss how these enzymes modify arachidonic acid and its analogues [40][41][42][43][44] as well as ceramides [27,45,46].…”
Section: Introductionmentioning
confidence: 99%