PTEN in neural precursor cells: Regulation of migration, apoptosis, and proliferation

被引:113
作者
Li, L
Liu, FH
Salmonsen, RA
Turner, TK
Litofsky, NS
Di Cristofano, A
Pandolfi, PP
Jones, SN
Recht, LD
Ross, AH
机构
[1] Univ Massachusetts, Sch Med, Dept Mol Pharmacol & Biochem, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Dept Neurol, Worcester, MA 01655 USA
[3] Univ Massachusetts, Sch Med, Dept Cell Biol, Worcester, MA 01655 USA
[4] Univ Massachusetts, Sch Med, Dept Surg Neurosurg, Worcester, MA 01655 USA
[5] Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10021 USA
[6] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
关键词
D O I
10.1006/mcne.2002.1115
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
PTEN is a lipid phosphatase, and PTEN mutations are associated with gliomas, macrocephaly, and mental deficiencies. We have used PTEN +/- mice to assess PTEN's role in subventricular zone (SVZ) precursor cells. For cultured SVZ neurosphere cells, haploinsufficiency for PTEN increases phosphorylation of Akt and forkhead transcription factor and slightly enhances proliferation. Based on a filter penetration assay, PTEN +/- cells are substantially more migratory and invasive than +/+ cells. The +/- cells also are more resistant to H2O2-induced apoptosis. Analysis of PTEN +/- and +/+ mice by BrdU labeling reveals no difference in the rate of cell proliferation in the SVZ. Exit of BrdU-labeled cells from the SVZ and radial migration to the outer layers of the olfactory bulb are more rapid for +/- cells. These observations indicate that PTEN regulates SVZ precursor cell function and is particularly important for migration and apoptosis in response to oxidative stress.
引用
收藏
页码:21 / 29
页数:9
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