Abstract
Molecular effects of pre-conditioning by 1-h hypoxia were investigated in cultured neurons from fetal rat forebrain, submitted the following day to a 6-h hypoxia that induces apoptosis. While preventing from apoptosis, pre-conditioning led to increased number of living neurons, DNA synthesis, with persistent overexpression of Bcl-2 and proliferating cell nuclear antigen (PCNA). Adaptative mechanisms would involve anti-apoptotic proteins and regulators of the cell cycle, to finally promote neuronal proliferation.
Copyright 1998 Elsevier Science B.V. All rights reserved.
MeSH terms
-
Animals
-
Apoptosis / drug effects
-
Apoptosis / physiology*
-
Cell Cycle
-
Cell Division
-
Cell Hypoxia*
-
Cells, Cultured
-
Culture Media, Serum-Free
-
DNA / biosynthesis
-
Epidermal Growth Factor / pharmacology
-
Fetus
-
Fibroblast Growth Factor 2 / pharmacology
-
Mitosis
-
Necrosis
-
Neurons / cytology*
-
Neurons / physiology*
-
Proliferating Cell Nuclear Antigen / biosynthesis
-
Prosencephalon / cytology*
-
Prosencephalon / physiology*
-
Proto-Oncogene Proteins c-bcl-2 / biosynthesis
-
Rats
-
Time Factors
Substances
-
Culture Media, Serum-Free
-
Proliferating Cell Nuclear Antigen
-
Proto-Oncogene Proteins c-bcl-2
-
Fibroblast Growth Factor 2
-
Epidermal Growth Factor
-
DNA