| Literature DB >> 15093680 |
Heidi S Phillips1, Merry Nishimura, Mark P Armanini, Karen Chen, Kathryn M Albers, Brian M Davis.
Abstract
Basal forebrain cholinergic (BFC) neurons are an important substrate of cognitive function and are hypothesized to require the presence of nerve growth factor (NGF) for survival and target innervation. NGF-deficient mice develop BFC neurons that extend projections into telencephalic targets, but the mice perish before innervation is fully established. Rescue of NGF-deficient mice by transgenic expression of NGF under the keratin promoter yields viable mice with disrupted CNS expression of NGF. In the current study, rescued NGF-deficient mice contain normal numbers of septal cholinergic neurons yet reveal severe compromise of cholinergic innervation of both cortex and hippocampus. Surprisingly, intracerebroventricular infusion of NGF into juvenile mice can induce an essentially normal pattern of cholinergic innervation of the hippocampus. These results indicate that NGF is required for induction of proper innervation by BFC neurons, but that the cellular pattern of expression of this factor is not critical for specifying the distribution of axon terminals.Entities:
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Year: 2004 PMID: 15093680 DOI: 10.1016/j.molbrainres.2003.01.001
Source DB: PubMed Journal: Brain Res Mol Brain Res ISSN: 0169-328X