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[Effects of leptin and insulin on leptin receptors mRNA expression in human hepatocellular HepG2 cells].

作者信息

Liu Zheng-Juan, Yao Xing-Jia, Wang Yu-Chuan, Wang De-Ying, Chen Zhu-Ming, Zhai Ling-Ling

机构信息

Department of Pediatrics, 2nd Hospital of Chinese Medical University, Shenyang 110004, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2005 Feb 16;85(6):396-9.

Abstract

OBJECTIVE

To study the leptin receptor isoforms regulation by leptin and insulin.

METHODS

Human hepatocellular carcinoma cells of the line HepG2 were cultured in DMEM containing 10% FBS in six-well plate and were incubated for 24 hours in serum-free medium containing 0, 10(-9), 10(-8), 10(-7), and 10(-6) mol/L of human leptin or insulin. Using the semi-quantitative RT-PCR technique, the mRNA expressions of long (OB-Rb) and short (OB-Ra: OB-R219.3) leptin receptor isoforms were measured.

RESULTS

OB-Rb and OB-R219.3 mRNAs were expressed in this cell line. Leptin of the concentrations of 10(-7) approximately 10(-6) mol/L significantly inhibited the OB-Rb mRNA expression, with the maximum decrease (by 43%) at the concentration of 10(-6) mol/L. Similarly the mRNA expression of OB-R219.3 was also markedly reduced in cells treated with leptin of the concentrations of 10(-8) approximately 10(-6) (mol/L), with the maximum inhibition (by 49%) at the concentrations of 10(-6) mol/L. Insulin showed no effect on OB-Rb and OB-R219.3 mRNAs expression in HepG2 cell.

CONCLUSION

In HepG2 cells, leptin down-regulates the expressions of OB-Rb and OB-R219.3 mRNAs, and insulin has no effect on OB-Rb and OB-R219.3 mRNAs, which contributes at least partly to an understanding of the mechanism of leptin resistance in vivo and suggests that leptin-induced receptor down-regulation may be relevant to leptin resistance at sites of peripheral action.

摘要

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