Premium
Short‐term Type‐1 diabetes differentially modulates 14‐3‐3 proteins in rat brain and liver
Author(s) -
Taurino Federica,
Stanca Eleonora,
Vonghia Luisa,
Siculella Luisa,
Sardanelli Anna Maria,
Papa Sergio,
Zanotti Franco,
Gi Antonio
Publication year - 2014
Publication title -
european journal of clinical investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.164
H-Index - 107
eISSN - 1365-2362
pISSN - 0014-2972
DOI - 10.1111/eci.12241
Subject(s) - messenger rna , endocrinology , medicine , streptozotocin , blot , diabetes mellitus , signal transduction , intraperitoneal injection , apoptosis , insulin , gene isoform , biology , cytosol , receptor , microbiology and biotechnology , biochemistry , gene , enzyme
Background The 14‐3‐3 proteins family consists of seven proteins that are highly conserved molecular chaperones with roles in the regulation of metabolism, signal transduction, cell cycle control, protein trafficking and apoptosis. Their role in several pathologies has been reported. In this study, we investigated the mRNA and protein expression of the 14‐3‐3s in rat brain and liver in the early stage of Type‐1 diabetes (T1D). Material and methods Diabetes was induced by a single intraperitoneal injection (70 mg/kg bw) of freshly prepared streptozotocin (STZ), and, after 3 weeks of treatment, brain and liver nuclei and cytosolic extracts were prepared. Quantitative real‐time PCR and Western blotting analyses were performed to evaluate mRNA and protein expression for each of the seven 14‐3‐3s. Results In nondiabetic control rats, the expression profile of 14‐3‐3s revealed a tissue‐specific distribution, and the expression level of each isoform was found higher in the brain than in the liver. In the diabetic brain, mRNA and protein levels of the 14‐3‐3β, ε, ζ, η and θ were lower; 14‐3‐3σ mRNA significantly increased while its protein level decreased. In the diabetic liver, the mRNA of 14‐3‐3γ, 14‐3‐3θ and 14‐3‐3σ significantly increased, but only the 14‐3‐3γ protein level increased. Overall, in diabetic animals, the changes in the expression levels of brain 14‐3‐3s were much more pronounced than in the liver. Conclusion Our results indicate that during the early phase of STZ ‐induced T1D, the 14‐3‐3 proteins are affected in an isoform‐ and tissue‐specific way.