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Biochem Biophys Res Commun. 2014 Feb 28;445(1):236-43. doi: 10.1016/j.bbrc.2014.01.187. Epub 2014 Feb 6.

Development of in vitro model of insulin receptor cleavage induced by high glucose in HepG2 cells.

Author information

1
Division of Molecular Genetics, Institute for Enzyme Research, Tokushima University, 3-18-15 Kuramotocho, Tokushima 770-8503, Japan.
2
Institute for Health Sciences, Tokushima Bunri University, Tokushima 770-8514, Japan.
3
Division of Molecular Genetics, Institute for Enzyme Research, Tokushima University, 3-18-15 Kuramotocho, Tokushima 770-8503, Japan. Electronic address: ebina@za3.so-net.ne.jp.

Abstract

Soluble insulin receptor (sIR), the ectodomain of IR, has been detected in human plasma, and its concentration parallels that of blood glucose in patients with diabetes. IR has a pivotal role in glucose homeostasis and diabetes development; therefore, cleavage of IR promoted by hyperglycemia is involved in insulin resistance and glucose toxicity. To elucidate the physiology of sIR, we developed an in vitro model mimicking the changes in sIR levels in plasma from patients with diabetes. Among four human cell lines that expressed IR, spontaneous cleavage of IR occurred only in HepG2 cells. The molecular characteristics of sIR derived from HepG2 cells were similar to those of sIR detected in human plasma. The concentration of sIR in the medium did not differ between basal and high-glucose conditions in the initial 24-h period, but increasing the duration of pre-stimulation (>48 h) led to a significant increase in sIR levels in cells exposed to high glucose. Additionally, glucose-dependent increment of sIR was reversible in this model. These results are consistent with the observation of plasma sIR in patients with diabetes. Using this model, O-linked N-acetylglucosamine modification was determined to be involved in high-glucose-induced IR cleavage. A calcium-dependent protease was shown to cleave IR extracellularly. These findings show that this in vitro model could be useful for determining the molecular mechanism underlying IR cleavage.

KEYWORDS:

Calcium-dependent protease; HepG2 cells; O-GlcNAcylation; Shedding; Soluble insulin receptor

PMID:
24508798
DOI:
10.1016/j.bbrc.2014.01.187
[Indexed for MEDLINE]

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