Maternal Choline Availability Alters the Localization of p15Ink4B and p27Kip1 Cyclin-Dependent Kinase Inhibitors in the Developing Fetal Rat Brain Hippocampus
- 1 April 2001
- journal article
- research article
- Published by S. Karger AG in Developmental Neuroscience
- Vol. 23 (2) , 100-106
- https://doi.org/10.1159/000048701
Abstract
Previously we have shown that changes in maternal dietary choline are associated with permanent behavioral changes in offspring. Importantly, in adult male rats, feeding a choline-deficient diet increases the localization of cyclin-dependent kinase inhibitors (CDKIs) in the liver, whereas young adult CDKI knockout mice (p15Ink4B or p27Kip1) exhibit behavioral abnormalities. Thus, maternal dietary choline-CDKI interactions could underlie the changes we observe in fetal hippocampal development and cognitive function in offspring. Here, timed-pregnant rats on embryonic day E12 were fed the AIN-76 diet with varying levels of dietary choline for 6 days, and, on E18, fetal brain sections were collected, and the localization of CDKI proteins was studied using immunohistochemistry and an unbiased image analysis method. In choline-supplemented animals compared to controls, the number of cells with nuclear immunoreactivity for p15Ink4b CDKI protein was decreased 2- to 3-fold in neuroepithelial ventricular zones and adjacent subventricular zones corresponding to the fimbria, primordial dentate gyrus and Ammon’s horn regions in the fetal hippocampus. In contrast, maternal dietary choline deficiency significantly decreased nuclear p15Ink4b immunoreactivity in the neuroepithelial layer of the dentate gyrus. Unlike p15Ink4b, the CDKI protein p27Kip1 was observed almost exclusively in the cytoplasm, though the protein was distributed throughout the proliferating and postmitotic zones in the E18 fetal hippocampus. Maternal dietary choline supplementation decreased the cytoplasmic staining intensity for p27Kip1 throughout the fetal hippocampus compared to control animals. Choline deficiency increased the staining intensity of p27Kip1 throughout the hippocampus in association with increased expression of MAP-1 and vimentin proteins. These results link maternal dietary choline availability to CDKI protein immunoreactivity and commitment to differentiation during fetal hippocampal development.Keywords
This publication has 10 references indexed in Scilit:
- Single or multiple oligodendroglial lineages: A controversyGlia, 1999
- Cell multiplication: Peering in and peering out: regulation of and by the cell cycleEditorial overviewCurrent Opinion in Cell Biology, 1999
- Postnatal neuronal proliferation in mice lacking Ink4d and Kip1 inhibitors of cyclin-dependent kinasesProceedings of the National Academy of Sciences, 1999
- Prenatal Availability of Choline Alters the Development of Acetylcholinesterase in the Rat HippocampusDevelopmental Neuroscience, 1999
- Ectopic expression of p27Kip1 in oligodendrocyte progenitor cells results in cell‐cycle growth arrestJournal of Neurobiology, 1998
- Tumor-suppressor p53 is expressed in proliferating and newly formed neurons of the embryonic and postnatal rat brain: Comparison with expression of the cell cycle regulators p21Waf1/Cip1, p27Kip1, p57Kip2, p16Ink4a, cyclin G1, and the proto-oncogene baxJournal of Comparative Neurology, 1998
- Cyclin‐dependent kinase inhibitor P27kip1 is expressed at high levels in cells that express a myelinating phenotypeJournal of Neuroscience Research, 1997
- Maternal protein restriction early in rat pregnancy alters brain development in the progenyDevelopmental Brain Research, 1997
- The brain-specific activator p35 allows Cdk5 to escape inhibition by p27Kip1 in neurons.Proceedings of the National Academy of Sciences, 1996
- Principles of CDK regulationNature, 1995