Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2006-11-22
pubmed:abstractText
We have found previously that pituitary adenylate cyclase-activating polypeptide (PACAP) increases the number of astrocytes generated from cultured mouse neural stem cells (NSCs) via a mechanism that is independent of the cyclic AMP/protein kinase A pathway (Ohno et al., 2005). In the present study, the signaling pathway involved in the differentiation process was further investigated. PACAP-induced differentiation was inhibited by the phospholipase C inhibitor, U73122, the protein kinase C (PKC) inhibitor, chelerythrine, and the intracellular calcium chelator, BAPTA-AM, and was mimicked by phorbol 12-myristate 13-acetate (PMA), but not by 4alpha-PMA. These results suggest that the PACAP-generated signal was mediated via the PACAP receptor, PAC1 stimulated heterotrimeric G-protein, resulting in activation of phospholipase C, followed by calcium- and phospholipid-dependent protein kinase C (cPKC). To elucidate the involvement of the different isoforms of cPKC, their gene and protein expression were examined. Embryonic NSCs expressed alpha and betaII PKC, but lacked PKCgamma. When NSCs were exposed to 2 nM PACAP, protein expression levels of the betaII isoform transiently increased two-fold before differentiation, returning to basal levels by Day 4, whereas the level of PKCalpha increased linearly up to Day 6. Overexpression of PKCbetaII with adenovirus vector synergistically enhanced differentiation in the presence of 1 nM PACAP, whereas expression of the dominant-negative mutant of PKCbetaII proved inhibitory. These results indicate that the beta isoform of PKC plays a crucial role in the PACAP-induced differentiation of mouse embryonic NSCs into astrocytes.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0360-4012
pubmed:author
pubmed:issnType
Print
pubmed:volume
84
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1645-55
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:17022039-Adenoviridae, pubmed-meshheading:17022039-Analysis of Variance, pubmed-meshheading:17022039-Animals, pubmed-meshheading:17022039-Astrocytes, pubmed-meshheading:17022039-Cell Count, pubmed-meshheading:17022039-Cell Differentiation, pubmed-meshheading:17022039-Cells, Cultured, pubmed-meshheading:17022039-Drug Interactions, pubmed-meshheading:17022039-Embryo, Mammalian, pubmed-meshheading:17022039-Enzyme Inhibitors, pubmed-meshheading:17022039-Gene Expression Regulation, Developmental, pubmed-meshheading:17022039-Glial Fibrillary Acidic Protein, pubmed-meshheading:17022039-Intermediate Filament Proteins, pubmed-meshheading:17022039-Mice, pubmed-meshheading:17022039-Mice, Inbred ICR, pubmed-meshheading:17022039-Nerve Tissue Proteins, pubmed-meshheading:17022039-Pituitary Adenylate Cyclase-Activating Polypeptide, pubmed-meshheading:17022039-Protein Isoforms, pubmed-meshheading:17022039-Protein Kinase C, pubmed-meshheading:17022039-RNA, Messenger, pubmed-meshheading:17022039-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:17022039-Stem Cells, pubmed-meshheading:17022039-Transfection
pubmed:year
2006
pubmed:articleTitle
Pituitary adenylate cyclase-activating polypeptide-induced differentiation of embryonic neural stem cells into astrocytes is mediated via the beta isoform of protein kinase C.
pubmed:affiliation
Department of Anatomy, School of Medicine, Showa University, Tokyo, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't