作者: Ewa Gurgul-Convey , Martin T. Kaminski , Sigurd Lenzen
DOI: 10.1016/J.BBRC.2015.05.072
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摘要: Abstract In the new human EndoC-βH1 β-cell line, a detailed analysis of physiological characteristics was performed. This line expressed all target structures on gene and protein level, which are crucial for function insulin secretion induced by glucose other secretagogues. Glucose influx measurements revealed an excellent uptake capacity β-cells Glut1 Glut2 transporters. A high expression level glucokinase enabled efficient phosphorylation, increasing ATP/ADP ratio along with stimulation in concentration range. The EC50 value 10.3 mM. Mannoheptulose, specific inhibitor, blocked glucose-induced (GSIS). nutrient secretagogues l -leucine 2-ketoisocaproate also stimulated secretion, potentiating effect -glutamine. Kir 6.2 potassium channel blocker glibenclamide Bay K 8644, opener voltage-sensitive Ca2+ significantly potentiated GSIS. Potentiation GSIS IBMX forskolin went strong cAMP generation. conclusion, fully mirrors analogous primary mouse, rat β-cells. Thus, this is very well suited studies.