Phosphoinositide-3-kinases p110α and p110β mediate S phase entry in astroglial cells in the marginal zone of rat neocortex
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Author
Contributions
- Fischer, Catharina 1977- Verfasser - Contributor
- Wilmes, Thomas 1979- Verfasser - Contributor
- Heimrich, Bernd 1956- Verfasser - Contributor
- Distel, Vanessa 1981- Verfasser - Contributor
- Klugbauer, Axel Verfasser - Contributor
and 5 more
- Meyer, Dieter K. Verfasser - Contributor
- Albert-Ludwigs-Universität Freiburg Institut für Experimentelle und Klinische Pharmakologie und Toxikologie - Contributor
- Albert-Ludwigs-Universität Freiburg Abteilung für Neuroanatomie - Contributor
- Albert-Ludwigs-Universität Freiburg Medizinische Fakultät - Contributor
- Albert-Ludwigs-Universität Freiburg - Contributor
Publication
2013 - Universität, Freiburg, Germany
Language
English
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0 pages
Identifiers
- Open LibraryOL37839580M
Classifications
- DDC611.018
Description
Abstract: In cells cultured from neocortex of newborn rats, phosphoinositide-3-kinases of class I regulate the DNA synthesis in a subgroup of astroglial cells. We have studied the location of these cells as well as the kinase isoforms which facilitate the S phase entry. Using dominant negative (dn) isoforms as well as selective pharmacological inhibitors we quantified S phase entry by nuclear labeling with bromodeoxyuridine (BrdU). Only in astroglial cells harvested from the marginal zone (MZ) of the neocortex inhibition of phosphoinositide-3-kinases reduced the nuclear labeling with BrdU, indicating that neocortical astroglial cells differ in the regulation of proliferation. The two kinase isoforms p110α and p110β were essential for S phase entry. p110α diminished the level of the p27Kip1 which inactivates the complex of cyclin E and CDK2 necessary for entry into the S phase. p110β phosphorylated and inhibited glycogen synthase kinase-3β which can prevent S-phase entry. Taken together, both isoforms mediated S phase in a subgroup of neocortical astroglial cells and acted via distinct pathways
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