TY - JOUR
T1 - Oxidative stress induced lipocalin 2 gene expression
T2 - Addressing its expression under the harmful conditions
AU - Roudkenar, Mehryar Habibi
AU - Kuwahara, Yoshikazu
AU - Baba, Taisuke
AU - Roushandeh, Amaneh Mohammadi
AU - Ebishima, Shigeko
AU - Abe, Shinya
AU - Ohkubo, Yasuhito
AU - Fukumoto, Manabu
PY - 2007
Y1 - 2007
N2 - Lipocalin 2 (Lcn2, NGAL) is a member of the lipocalin superfamily with diverse functions such as the transport of fatty acids and the induction of apoptosis. Previous reports indicated that expression of Lcn2 is induced under harmful conditions. However, the mechanisms of the induction of Lcn2 expression remain to be elucidated. In this report, we intended to identify the factor or factors that induce Lcn2 expression. Up-regulation of Lcn2 expression after X-ray exposure was detected in the heart, the kidney and especially in the liver. Primary culture of liver component cells revealed that this up-regulation in the liver was induced in hepatocytes. Up-regulation of Lcn2 expression was also detected in HepG2 cells after the administration of X-rays or H 2O2. Interestingly, up-regulation of Lcn2 expression after H2O2 treatment was canceled by the addition of the anti-oxidants, dimethylsulfoxide or cysteamine. These results strongly suggest that Lcn2 expression is induced by reactive oxygen species. Therefore, Lcn2 could be a useful biomarker to identify oxidative stress both in vitro and in vivo.
AB - Lipocalin 2 (Lcn2, NGAL) is a member of the lipocalin superfamily with diverse functions such as the transport of fatty acids and the induction of apoptosis. Previous reports indicated that expression of Lcn2 is induced under harmful conditions. However, the mechanisms of the induction of Lcn2 expression remain to be elucidated. In this report, we intended to identify the factor or factors that induce Lcn2 expression. Up-regulation of Lcn2 expression after X-ray exposure was detected in the heart, the kidney and especially in the liver. Primary culture of liver component cells revealed that this up-regulation in the liver was induced in hepatocytes. Up-regulation of Lcn2 expression was also detected in HepG2 cells after the administration of X-rays or H 2O2. Interestingly, up-regulation of Lcn2 expression after H2O2 treatment was canceled by the addition of the anti-oxidants, dimethylsulfoxide or cysteamine. These results strongly suggest that Lcn2 expression is induced by reactive oxygen species. Therefore, Lcn2 could be a useful biomarker to identify oxidative stress both in vitro and in vivo.
KW - HO
KW - Lipocalin 2
KW - Liver
KW - Oxidative stress
KW - Radiation
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UR - http://www.scopus.com/inward/citedby.url?scp=33846888090&partnerID=8YFLogxK
U2 - 10.1269/jrr.06057
DO - 10.1269/jrr.06057
M3 - Article
C2 - 17229997
AN - SCOPUS:33846888090
VL - 48
SP - 39
EP - 44
JO - Journal of Radiation Research
JF - Journal of Radiation Research
SN - 0449-3060
IS - 1
ER -