Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Gewählte Publikation:
Hay, JC; Fisette, PL; Jenkins, GH; Fukami, K; Takenawa, T; Anderson, RA; Martin, TF.
ATP-dependent inositide phosphorylation required for Ca(2+)-activated secretion.
Nature. 1995; 374(6518):173-177
Doi: 10.1038/374173a0
Web of Science
PubMed
FullText
FullText_MUG
- Führende Autor*innen der Med Uni Graz
- Hay Jesse
- Altmetrics:
- Dimensions Citations:
- Plum Analytics:
- Scite (citation analytics):
- Abstract:
- Regulated fusion of secretory granules with the plasma membrane in secretory cells requires ATP, Ca2+ and cytosolic as well as membrane proteins. ATP-dependent steps in Ca(2+)-activated secretion from PC12 cells require three cytosolic PEP proteins (priming in exocytosis proteins, PEP1-3), the identity of which will provide insights into the required ATP-using reactions. PEP3 was recently identified as phosphatidylinositol transfer protein (PtdInsTP), and here we report that PEP1 consists of the type I phosphatidylinositol-4-phosphate 5-kinase (PtdInsP5K). The roles of PEP3/PtdInsTP and PEP1/PtdInsP5K in sequential phosphoinositide recruitment and phosphorylation explains their synergistic activity in ATP-dependent priming. Moreover, inhibition of Ca(2+)-activated secretion by PtdIns(4,5)P2-specific antibodies and phospholipase C implies that 5-phosphorylated inositides play a novel, necessary role in the regulated secretory pathway. The results indicate that lipid kinase-mediated phosphorylation is an important basis for ATP use in the exocytotic pathway.
- Find related publications in this database (using NLM MeSH Indexing)
- Adenosine Triphosphate - metabolism
- Animals -
- Calcium - metabolism
- Carrier Proteins - metabolism
- Cattle -
- Cytosol - metabolism
- Exocytosis -
- Membrane Proteins -
- Norepinephrine - secretion
- PC12 Cells -
- Phosphatidylinositols - metabolism
- Phospholipid Transfer Proteins -
- Phosphorylation -
- Phosphotransferases (Alcohol Group Acceptor) - antagonists & inhibitors
- Phosphotransferases (Alcohol Group Acceptor) - metabolism
- Rats -
- Type C Phospholipases - metabolism