Title : A role for MRP8 in in stent restenosis in diabetes.

Pub. Date : 2012 Apr

PMID : 22381691






7 Functional Relationships(s)
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Protein Name
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1 Expression of MRP8/14 was also elevated in EC exposed to high glucose conditions. Glucose ATP binding cassette subfamily C member 8 Homo sapiens
2 EC function was impaired by high glucose concentrations, and this effect could be mimicked by MRP8 over-expression. Glucose ATP binding cassette subfamily C member 8 Homo sapiens
3 MRP8 knockdown by shRNA significantly restored EC function after exposure to high glucose concentrations. Glucose ATP binding cassette subfamily C member 8 Homo sapiens
4 MRP8 expression in glucose exposed cells was also inhibited using pharmacological blockade of glucose-induced pathways. Glucose ATP binding cassette subfamily C member 8 Homo sapiens
5 MRP8 expression in glucose exposed cells was also inhibited using pharmacological blockade of glucose-induced pathways. Glucose ATP binding cassette subfamily C member 8 Homo sapiens
6 CONCLUSIONS: EC dysfunction caused by elevated glucose levels could be mimicked by MRP8/14 over-expression and reversed/prevented by MRP8 knockdown. Glucose ATP binding cassette subfamily C member 8 Homo sapiens
7 CONCLUSIONS: EC dysfunction caused by elevated glucose levels could be mimicked by MRP8/14 over-expression and reversed/prevented by MRP8 knockdown. Glucose ATP binding cassette subfamily C member 8 Homo sapiens