TY - JOUR
T1 - Effect of lipopolysaccharide on the gene expression of the enzymes involved in tetrahydrobiopterin de novo biosynthesis in murine neuroblastoma cell line N1E-115
AU - Mori, Keiji
AU - Nakashima, Akira
AU - Nagatsu, Toshiharu
AU - Ota, Akira
N1 - Funding Information:
This work was supported by Grants-in-Aid from the Ministry of education, Science, Sports and Culture of Japan to T.N. and by Grants-In-Aid from Fujita Health University, Japan to A.O. and T.N. We appreciate Dr. Haruhiro Higashida (Kanazawa University, Kanazawa, Japan) for his generous supply of N1E-115 cells. We thank Ms. Reiko Furuié for technical assistance.
PY - 1997/11/28
Y1 - 1997/11/28
N2 - The amounts of messenger RNA for three enzymes, namely guanosine triphosphate (GTP) cyclohydrolase I, 6-pyruvoyltetrahydropterin synthase, and sepiapterin reductase, all of which are involved in the de novo biosynthesis of (6R)-L-erythrodihydroxypropyl-2-amino-4-hydroxy-5,6,7,8- tetrahydropteridine (BH4) from GTP, were measured quantitatively in murine neuroblastoma cell line N1E-115 by the competitive polymerase chain reaction (PCR) technique after reverse transcription using a heterologous DNA fragment as an internal standard. Twenty-four hour activation of this cell line with 1 μg/ml lipopolysaccharide resulted in statistically significant increases in the amounts of the messages of all three enzymes. Our data suggest that lipopolysaccharide can activate the intrinsic pathway resulting in the enhanced gene expression of these three enzymes in neuron-derived cells such as N1E-115.
AB - The amounts of messenger RNA for three enzymes, namely guanosine triphosphate (GTP) cyclohydrolase I, 6-pyruvoyltetrahydropterin synthase, and sepiapterin reductase, all of which are involved in the de novo biosynthesis of (6R)-L-erythrodihydroxypropyl-2-amino-4-hydroxy-5,6,7,8- tetrahydropteridine (BH4) from GTP, were measured quantitatively in murine neuroblastoma cell line N1E-115 by the competitive polymerase chain reaction (PCR) technique after reverse transcription using a heterologous DNA fragment as an internal standard. Twenty-four hour activation of this cell line with 1 μg/ml lipopolysaccharide resulted in statistically significant increases in the amounts of the messages of all three enzymes. Our data suggest that lipopolysaccharide can activate the intrinsic pathway resulting in the enhanced gene expression of these three enzymes in neuron-derived cells such as N1E-115.
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U2 - 10.1016/S0304-3940(97)00833-1
DO - 10.1016/S0304-3940(97)00833-1
M3 - Article
C2 - 9464645
AN - SCOPUS:0031459854
SN - 0304-3940
VL - 238
SP - 21
EP - 24
JO - Neuroscience Letters
JF - Neuroscience Letters
IS - 1-2
ER -