TY - JOUR
T1 - Significant modulation of the hepatic proteome induced by exposure to low temperature in Xenopus laevis
AU - Nagasawa, Kazumichi
AU - Tanizaki, Yuta
AU - Okui, Takehito
AU - Watarai, Atsuko
AU - Ueda, Shinobu
AU - Kato, Takashi
N1 - Funding Information:
This work was supported in part by a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science; by Health and Labour Sciences Research Grants from the Ministry of Health, Labour and Welfare (MHLW); by Research on Seeds for Publicly Essential Drugs and Medical Devices (from the MHLW); by a Strategic Research Foundation Grant-aided Project for Private Universities from the Japanese Ministry of Education, Culture, Sports, Science, and Technology (MEXT); and by Waseda University grants for special research projects. Part of this study was performed as a component of a Private University ‘‘High-Tech Research Center’’ project supported by MEXT.
Publisher Copyright:
© 2013 Published by The Company of Biologists Ltd.
PY - 2013/10/15
Y1 - 2013/10/15
N2 - The African clawed frog, Xenopus laevis, is an ectothermic vertebrate that can survive at low environmental temperatures. To gain insight into the molecular events induced by low body temperature, liver proteins were evaluated at the standard laboratory rearing temperature (22°C, control) and a low environmental temperature (5°C, cold exposure). Using nano-flow liquid chromatography coupled with tandem mass spectrometry, we identified 58 proteins that differed in abundance. A subsequent Gene Ontology analysis revealed that the tyrosine and phenylalanine catabolic processes were modulated by cold exposure, which resulted in decreases in hepatic tyrosine and phenylalanine, respectively. Similarly, levels of pyruvate kinase and enolase, which are involved in glycolysis and glycogen synthesis, were also decreased, whereas levels of glycogen phosphorylase, which participates in glycogenolysis, were increased. Therefore, we measured metabolites in the respective pathways and found that levels of hepatic glycogen and glucose were decreased. Although the liver was under oxidative stress because of iron accumulation caused by hepatic erythrocyte destruction, the hepatic NADPH/NADP ratio was not changed. Thus, glycogen is probably utilized mainly for NADPH supply rather than for energy or glucose production. In conclusion, X. laevis responds to low body temperature by modulating its hepatic proteome, which results in altered carbohydrate metabolism.
AB - The African clawed frog, Xenopus laevis, is an ectothermic vertebrate that can survive at low environmental temperatures. To gain insight into the molecular events induced by low body temperature, liver proteins were evaluated at the standard laboratory rearing temperature (22°C, control) and a low environmental temperature (5°C, cold exposure). Using nano-flow liquid chromatography coupled with tandem mass spectrometry, we identified 58 proteins that differed in abundance. A subsequent Gene Ontology analysis revealed that the tyrosine and phenylalanine catabolic processes were modulated by cold exposure, which resulted in decreases in hepatic tyrosine and phenylalanine, respectively. Similarly, levels of pyruvate kinase and enolase, which are involved in glycolysis and glycogen synthesis, were also decreased, whereas levels of glycogen phosphorylase, which participates in glycogenolysis, were increased. Therefore, we measured metabolites in the respective pathways and found that levels of hepatic glycogen and glucose were decreased. Although the liver was under oxidative stress because of iron accumulation caused by hepatic erythrocyte destruction, the hepatic NADPH/NADP ratio was not changed. Thus, glycogen is probably utilized mainly for NADPH supply rather than for energy or glucose production. In conclusion, X. laevis responds to low body temperature by modulating its hepatic proteome, which results in altered carbohydrate metabolism.
KW - Animal model
KW - Liver
KW - Low temperature
KW - Pathway
KW - Proteomics
KW - Xenopus laevis
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U2 - 10.1242/bio.20136106
DO - 10.1242/bio.20136106
M3 - Article
AN - SCOPUS:84979499884
SN - 2046-6390
VL - 2
SP - 1057
EP - 1069
JO - Biology Open
JF - Biology Open
IS - 10
ER -