Elena Lima-Cabello1, Victor Alche2, Rhonda C Foley3, Sofianos Andrikopoulos4, Grant Morahan5, Karam B Singh3,6, Juan D Alche1, Jose C Jimenez-Lopez1,6. 1. Plant Reproductive Biology Laboratory; Deptartment of Biochemistry, Cell & Molecular Biology of Plants, Estacion Experimental del Zaidin, Spanish National Research Council (CSIC), Granada, Spain. 2. Andalusian Health System, Health Center "Villanueva de las Torres", Granada, Spain. 3. The Commonwealth Scientific and Industrial Research Organisation (CSIRO), Agriculture and Food, Centre for Environment and Life Sciences (CELS); Floreat, WA, Australia. 4. Department of Medicine, Heidelberg Repatriation Hospital, The University of Melbourne, Heidelberg West, VIC, Australia. 5. Harry Perkins Institute of Medical Research, Centre for Diabetes Research, The University of Western Australia, Perth, WA, Australia. 6. The UWA Institute of Agriculture, The University of Western Australia, Perth, WA, Australia.
Abstract
SCOPE: We have investigated the potential use of β-conglutin protein isoforms from narrow-leafed lupin (Lupinus angustifolius L.) as a diabetes treatment. METHODS AND RESULTS: We produced purified recombinant β1-, β2-, β3-, β4-, and β6-conglutin proteins and showed that β1, β3, and β6 could bind to insulin. To assess β-conglutin proteins modulatory effect on insulin activation meditated kinases, whole blood and peripheral blood mononuclear cell cultures from type 2 diabetes (T2D) and healthy control subjects (C) were incubated with conglutin proteins. The treatment of peripheral blood mononuclear cells from T2D patients with β1, β3, and β6 proteins increased up to threefold mRNA and protein levels of genes important in insulin signaling pathways, namely insulin receptor substrate 1/p85/AKT/glucose transporter type 4. This was accompanied by a comparable fold-change decrease in the mRNA expression level of pro-inflammatory genes (iNOS and IL-1β) and proteins compared to healthy controls. The β2 and β4 isoforms had no effect on the insulin signaling pathway. However, these β-conglutin proteins elicited pro-inflammatory effects since levels of mRNA and proteins of inducible nitric oxide synthase and IL 1 beta were increased. CONCLUSION: Our results raise the possibility of using these particular β-conglutin proteins in the prevention and treatment of diabetes, as well as their potential as anti-inflammatory molecules.
SCOPE: We have investigated the potential use of β-conglutin protein isoforms from narrow-leafed lupin (Lupinus angustifolius L.) as a diabetes treatment. METHODS AND RESULTS: We produced purified recombinant β1-, β2-, β3-, β4-, and β6-conglutin proteins and showed that β1, β3, and β6 could bind to insulin. To assess β-conglutin proteins modulatory effect on insulin activation meditated kinases, whole blood and peripheral blood mononuclear cell cultures from type 2 diabetes (T2D) and healthy control subjects (C) were incubated with conglutin proteins. The treatment of peripheral blood mononuclear cells from T2D patients with β1, β3, and β6 proteins increased up to threefold mRNA and protein levels of genes important in insulin signaling pathways, namely insulin receptor substrate 1/p85/AKT/glucose transporter type 4. This was accompanied by a comparable fold-change decrease in the mRNA expression level of pro-inflammatory genes (iNOS and IL-1β) and proteins compared to healthy controls. The β2 and β4 isoforms had no effect on the insulin signaling pathway. However, these β-conglutin proteins elicited pro-inflammatory effects since levels of mRNA and proteins of inducible nitric oxide synthase and IL 1 beta were increased. CONCLUSION: Our results raise the possibility of using these particular β-conglutin proteins in the prevention and treatment of diabetes, as well as their potential as anti-inflammatory molecules.
Authors: Elena Lima-Cabello; Juan D Alché; Sonia Morales-Santana; Alfonso Clemente; Jose C Jimenez-Lopez Journal: Antioxidants (Basel) Date: 2019-12-23
Authors: Adoración Zafra; Mohammed M'rani-Alaoui; Elena Lima; Jose Carlos Jimenez-Lopez; Juan de Dios Alché Journal: Front Plant Sci Date: 2018-10-12 Impact factor: 5.753