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P2 receptor stimulation induces amyloid precursor protein production and secretion in rat cortical astrocytes
Authors:Tran Minh D
Affiliation:Research Service 151, Miami VAMC, 1201 NW 16th Street, Miami, FL 33125, United States. Minh.Tran@va.gov
Abstract:
Amyloid precursor protein (APP) is ubiquitously expressed in a variety of tissues but is predominantly expressed in the brain. The expression of APP has been well studied in neurons but little is known about its presence in astrocytes. The study presented here shows that purinergic signaling is involved in the production and secretion of APP in primary cultures of rat cortical astrocytes. Extracellular ATP caused an increase in APP production and release in a time- and concentration-dependent manner and was inhibited by antagonists of P2 receptors. Further agonist and antagonist studies revealed involvement of P2Y2 and P2Y4 receptors in nucleotide-stimulated production and release of APP. In addition, signaling studies with various protein kinase inhibitors demonstrated that blockade of mitogen-activated protein kinases, but not Akt, inhibited nucleotide-stimulated APP expression and release. These results indicate that APP production and secretion can be regulated by activation of P2Y2/4 receptors coupled to protein kinase signaling pathways and suggest that astrocytes can be a potential source of APP.
Keywords:2MeSADP, 2-methylthio-ADP   8PSPT, 8-(p-sulfophenyl)-theophylline   AD, Alzheimer's disease   APP, amyloid precursor protein   BzATP, 3′-O-(4-benzoyl)benzoyl-ATP   DAPI, 4′-6-diamidino-2-phenylindole   DMEM, Dulbecco's modified Eagle's medium   ERK, extracellular signal regulated protein kinase   MAPK, mitogen-activated protein kinase   MEK, MAPK/ERK kinase   NECA, N-ethylcarboxamidoadenosine   NGF, nerve growth factor   PI3K, phosphatidylinositol 3-kinase   PPADS, pyridoxalphosphate-6-azophenyl-2′-4′-disulfonice acid   RB2, reactive blue 2   SAPK/JNK, stress-activated protein kinase/c-Jun N-terminal kinase   SB, SB202190   SP, SP600125
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