Short‐term Type‐1 diabetes differentially modulates 14‐3‐3 proteins in rat brain and liver. (21st February 2014)
- Record Type:
- Journal Article
- Title:
- Short‐term Type‐1 diabetes differentially modulates 14‐3‐3 proteins in rat brain and liver. (21st February 2014)
- Main Title:
- Short‐term Type‐1 diabetes differentially modulates 14‐3‐3 proteins in rat brain and liver
- Authors:
- Taurino, Federica
Stanca, Eleonora
Vonghia, Luisa
Siculella, Luisa
Sardanelli, Anna Maria
Papa, Sergio
Zanotti, Franco
Gnoni, Antonio - Abstract:
- <abstract abstract-type="main" id="eci12241-abs-0001"> <title>Abstract</title> <sec id="eci12241-sec-0001" sec-type="section"> <title>Background</title> <p>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).</p> </sec> <sec id="eci12241-sec-0002" sec-type="section"> <title>Material and methods</title> <p>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.</p> </sec> <sec id="eci12241-sec-0003" sec-type="section"> <title>Results</title> <p>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<abstract abstract-type="main" id="eci12241-abs-0001"> <title>Abstract</title> <sec id="eci12241-sec-0001" sec-type="section"> <title>Background</title> <p>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).</p> </sec> <sec id="eci12241-sec-0002" sec-type="section"> <title>Material and methods</title> <p>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.</p> </sec> <sec id="eci12241-sec-0003" sec-type="section"> <title>Results</title> <p>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.</p> </sec> <sec id="eci12241-sec-0004" sec-type="section"> <title>Conclusion</title> <p>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.</p> </sec> </abstract> … (more)
- Is Part Of:
- European journal of clinical investigation. Volume 44:Number 4(2014:Apr.)
- Journal:
- European journal of clinical investigation
- Issue:
- Volume 44:Number 4(2014:Apr.)
- Issue Display:
- Volume 44, Issue 4 (2014)
- Year:
- 2014
- Volume:
- 44
- Issue:
- 4
- Issue Sort Value:
- 2014-0044-0004-0000
- Page Start:
- 350
- Page End:
- 358
- Publication Date:
- 2014-02-21
- Subjects:
- Pathology -- Periodicals
Medical research -- Periodicals
616.075 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2362 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/eci.12241 ↗
- Languages:
- English
- ISSNs:
- 0014-2972
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.727100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4201.xml