Why the study?
Human cohort studies suggest the ApoB100/ApoAI ratio may be a risk factor in coronary heart disease, but its changes in response to varying glucose levels required in vitro evaluation.
Does higher glucose concentration increase the ApoB100/ApoAI ratio in cultured HepG2 cells?
Does higher glucose concentration increase the ApoB100/ApoAI ratio in cultured HepG2 cells?
Higher glucose concentrations increase the ApoB100/ApoAI ratio in HepG2 cells, providing an in vitro model for understanding lipoprotein changes related to coronary artery disease risk.
Answers are grounded in this paper and cite their sources.
Glucose raises ApoB100/ApoAI secretion ratio in HepG2 cells; leaves open any role in human CHD risk assessment.
<ns3:p> <ns3:bold>Backgroundː</ns3:bold> Numerous <ns3:italic>in vivo</ns3:italic> human cohort studies have suggested that the apolipoprotein B100/apolipoprotein AI (ApoB100/ApoAI) ratio might be a risk factor in coronary heart disease. The aim of this study was to measure ApoB100/ApoAI ratio changes in cell secretions by incubating HepG2 cells with various amounts of glucose <ns3:italic>in vitro</ns3:italic> . </ns3:p> <ns3:p> <ns3:bold>Methods</ns3:bold> <ns3:bold>ː</ns3:bold> HepG2 cells were cultured in low-, normal- or high-glucose Dulbecco's Modified Eagle Medium (DMEM) (1, 4.5 and 10g/L, respectively). Levels of ApoAI and ApoB100 were measured with commercial sandwich enzyme-linked immunosorbent assay kits (cat#: H0123 and H0124) from ShangHai MEIXUAN Biological Science and Technology Ltd (Shanghai, China). Experiments were repeated six times for each assay. </ns3:p> <ns3:p> <ns3:bold>Resultsː</ns3:bold> The results showed that ApoB100/ApoAI ratio have positive correlations with the glucose concentration increase. </ns3:p> <ns3:p> <ns3:bold>Conclusionsː</ns3:bold> A higher concentration of glucose induced an undesirable ApoB100/ApoAI ratio change, which suggests a new regulatory pathway in lipoprotein catabolism and provides a cell model for further mechanism study. This finding may lead to novel therapeutic ways for diagnosis and treatment for coronary artery disease. </ns3:p>
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Minshan Hu (2022) studied this question.
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