Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/13483
Title: Transduction mechanisms of P2Z purinoceptors.
Authors: Wiley, J S;Chen, J R;Snook, M S;Gargett, C E;Jamieson, Gary P
Affiliation: Haematology Department, Austin Hospital, Heidelberg, Victoria, Australia.
Issue Date: 16-May-1996
Citation: Ciba Foundation Symposium; 198(): 149-60; discussion 160-5
Abstract: The ability of extracellular ATP to increase the cation permeability of a variety of fresh and cultured cells has been known for decades, but evidence of a separate class of P2 purinoceptor, termed P2Z, which mediates this effect has only recently been obtained. Several features of the P2Z purinoceptor clearly distinguish it from other P2 purinoceptors and show that it is a ligand-gated ion channel. P2Z purinoceptors are highly selective for the ATP4- species and addition of Mg2+ in excess over ATP closes the channel. The most potent agonist is 3'-O-(4-benzoyl)benzoyl ATP which has a 10-fold lower EC50 than ATP. Ca2+ is the preferred permeant for the P2Z ion channel although it will pass ions up to the size of ethidium(+) (314 Da) in lymphocytes or fura-2 (813 Da) in macrophages. The inhibitors of the P2Z purinoceptor or its associated ion channel include suramin, amiloride analogues, high extracellular Na+ concentrations and 2',3'-dialdehyde ATP (oxidized ATP), which blocks irreversibly. Occupancy of P2Z purinoceptors stimulates a phospholipase D activity, which may be involved in membrane remodelling. Moreover, extracellular ATP causes loss of the glycosylated adhesion molecule L-selection from the surfaces of human lymphocytes by enzymic cleavage, suggesting a possible role for P2Z purinoceptors in intercellular interactions.
Internal ID Number: 8879824
URI: http://ahro.austin.org.au/austinjspui/handle/1/13483
URL: http://www.ncbi.nlm.nih.gov/pubmed/8879824
Type: Journal Article
Subjects: Adenosine Triphosphate.pharmacology
Animals
Down-Regulation
Enzyme Activation
Humans
Ion Channels.antagonists & inhibitors.metabolism
L-Selectin.metabolism
Lymphocytes.drug effects.metabolism
Phospholipase D.metabolism
Purinergic P2 Receptor Agonists
Purinergic P2 Receptor Antagonists
Receptors, Purinergic P2.metabolism
Receptors, Purinergic P2X7
Signal Transduction.physiology
Sodium.pharmacology
Appears in Collections:Journal articles

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