TY - JOUR
T1 - The LIM homeobox gene, L3/Lhx8, is necessary for proper development of basal forebrain cholinergic neurons
AU - Mori, Tetsuji
AU - Yuxing, Zhang
AU - Takaki, Hiromi
AU - Takeuchi, Mayumi
AU - Iseki, Ken
AU - Hagino, Seita
AU - Kitanaka, Jun Ichi
AU - Takemura, Motohiko
AU - Misawa, Hidemi
AU - Ikawa, Masahito
AU - Okabe, Masaru
AU - Wanaka, Akio
PY - 2004/6
Y1 - 2004/6
N2 - Basal forebrain cholinergic neurons (BFCNs) are involved in cognitive functions such as learning and memory, and are affected in several neurodegenerative diseases (e.g. Alzheimer's disease). Despite their importance, the molecular mechanisms of their development are not fully elucidated. A recent report demonstrated that some BFCNs in adult rat are positive for L3/Lhx8, a LIM homeobox transcription factor. To examine the function of L3/Lhx8 in the development of BFCNs, we generated L3/Lhx8 gene-disrupted mice. In these mice, cells expressing cholinergic neuron markers, such as choline acetyltransferase, vesicular acetylcholine transporter and p75 low-affinity NGF receptor, were markedly reduced in the basal forebrain, whereas other cholinergic neurons including brain stem and spinal motor neurons expressed the markers. Neurotransmitter phenotypes other than cholinergic in the basal forebrain appeared intact. From these results, we suggested that L3/Lhx8 has a pivotal and specific role in the development and/or maintenance of BFCNs.
AB - Basal forebrain cholinergic neurons (BFCNs) are involved in cognitive functions such as learning and memory, and are affected in several neurodegenerative diseases (e.g. Alzheimer's disease). Despite their importance, the molecular mechanisms of their development are not fully elucidated. A recent report demonstrated that some BFCNs in adult rat are positive for L3/Lhx8, a LIM homeobox transcription factor. To examine the function of L3/Lhx8 in the development of BFCNs, we generated L3/Lhx8 gene-disrupted mice. In these mice, cells expressing cholinergic neuron markers, such as choline acetyltransferase, vesicular acetylcholine transporter and p75 low-affinity NGF receptor, were markedly reduced in the basal forebrain, whereas other cholinergic neurons including brain stem and spinal motor neurons expressed the markers. Neurotransmitter phenotypes other than cholinergic in the basal forebrain appeared intact. From these results, we suggested that L3/Lhx8 has a pivotal and specific role in the development and/or maintenance of BFCNs.
KW - Brain
KW - Choline acetyltransferase
KW - LIM domain
KW - Mouse
KW - Null mutant
KW - Transcription factor
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U2 - 10.1111/j.0953-816X.2004.03415.x
DO - 10.1111/j.0953-816X.2004.03415.x
M3 - Article
C2 - 15217369
AN - SCOPUS:3042793746
SN - 0953-816X
VL - 19
SP - 3129
EP - 3141
JO - European Journal of Neuroscience
JF - European Journal of Neuroscience
IS - 12
ER -