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    The p75 neurotrophin receptor is expressed by adult mouse dentate progenitor cells and regulates neuronal and non-neuronal cell genesis

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    <p>Abstract</p> <p>Background</p> <p>The ability to regulate neurogenesis in the adult dentate gyrus will require further identification and characterization of the receptors regulating this process. <it>In vitro </it>and <it>in vivo </it>studies have demonstrated that neurotrophins and the p75 neurotrophin receptor (p75<sup>NTR</sup>) can promote neurogenesis; therefore we tested the hypothesis that p75<sup>NTR </sup>is expressed by adult dentate gyrus progenitor cells and is required for their proliferation and differentiation.</p> <p>Results</p> <p>In a first series of studies focusing on proliferation, mice received a single BrdU injection and were sacrificed 2, 10 and 48 hours later. Proliferating, BrdU-positive cells were found to express p75<sup>NTR</sup>. In a second series of studies, BrdU was administered by six daily injections and mice were sacrificed 1 day later. Dentate gyrus sections demonstrated a large proportion of BrdU/p75<sup>NTR </sup>co-expressing cells expressing either the NeuN neuronal or GFAP glial marker, indicating that p75<sup>NTR </sup>expression persists at least until early stages of maturation. In p75<sup>NTR </sup>(-/-) mice, there was a 59% decrease in the number of BrdU-positive cells, with decreases in the number of BrdU cells co-labeled with NeuN, GFAP or neither marker of 35%, 60% and 64%, respectively.</p> <p>Conclusions</p> <p>These findings demonstrate that p75<sup>NTR </sup>is expressed by adult dentate progenitor cells and point to p75<sup>NTR </sup>as an important receptor promoting the proliferation and/or early maturation of not only neural, but also glial and other cell types.</p
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