Expression of Syntaxin 8 in Visceral Adipose Tissue Is Increased in Obese Patients with Type 2 Diabetes and Related to Markers of Insulin Resistance and Inflammation
Obesity is associated with increased adipose tissue inflammation as well as with the development of type 2 diabetes (T2D). Syntaxin 8 (STX8) is a protein required for the transport of endosomes. In this study we analyzed the relationship of STX8 with the presence of T2D in the context of obesity. Wi...
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Published in | Archives of medical research Vol. 46; no. 1; pp. 47 - 53 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.01.2015
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ISSN | 0188-4409 1873-5487 1873-5487 |
DOI | 10.1016/j.arcmed.2014.12.003 |
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Abstract | Obesity is associated with increased adipose tissue inflammation as well as with the development of type 2 diabetes (T2D). Syntaxin 8 (STX8) is a protein required for the transport of endosomes. In this study we analyzed the relationship of STX8 with the presence of T2D in the context of obesity.
With this purpose, 21 subjects (seven lean [LN], eight obese normoglycemic [OB-NG] and six obese with type 2 diabetes [OB-T2D]) were included in the study. Gene and protein expression levels of STX8 and GLUT4 were analyzed in visceral adipose tissue (VAT).
mRNA (p = 0.008) and protein (p <0.001) expression levels of STX8 were significantly increased in VAT of OB-T2D patients. Moreover, gene expression levels of SLC2A4 (GLUT4) were downregulated (p = 0.002) in VAT of obese patients. We found that STX8 was positively correlated (p <0.05) with fasting glucose concentrations, plasma glucose 2 h after an OGTT and C-reactive protein. Interestingly, the expression of STX8 was negatively correlated (p <0.05) with the expression of SLC2A4 in VAT.
Increased STX8 expression in VAT appears to be associated with the presence of T2D in obese patients through a mechanism that may involve GLUT4. |
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AbstractList | Obesity is associated with increased adipose tissue inflammation as well as with the development of type 2 diabetes (T2D). Syntaxin 8 (STX8) is a protein required for the transport of endosomes. In this study we analyzed the relationship of STX8 with the presence of T2D in the context of obesity.
With this purpose, 21 subjects (seven lean [LN], eight obese normoglycemic [OB-NG] and six obese with type 2 diabetes [OB-T2D]) were included in the study. Gene and protein expression levels of STX8 and GLUT4 were analyzed in visceral adipose tissue (VAT).
mRNA (p = 0.008) and protein (p <0.001) expression levels of STX8 were significantly increased in VAT of OB-T2D patients. Moreover, gene expression levels of SLC2A4 (GLUT4) were downregulated (p = 0.002) in VAT of obese patients. We found that STX8 was positively correlated (p <0.05) with fasting glucose concentrations, plasma glucose 2 h after an OGTT and C-reactive protein. Interestingly, the expression of STX8 was negatively correlated (p <0.05) with the expression of SLC2A4 in VAT.
Increased STX8 expression in VAT appears to be associated with the presence of T2D in obese patients through a mechanism that may involve GLUT4. Obesity is associated with increased adipose tissue inflammation as well as with the development of type 2 diabetes (T2D). Syntaxin 8 (STX8) is a protein required for the transport of endosomes. In this study we analyzed the relationship of STX8 with the presence of T2D in the context of obesity.BACKGROUND AND AIMSObesity is associated with increased adipose tissue inflammation as well as with the development of type 2 diabetes (T2D). Syntaxin 8 (STX8) is a protein required for the transport of endosomes. In this study we analyzed the relationship of STX8 with the presence of T2D in the context of obesity.With this purpose, 21 subjects (seven lean [LN], eight obese normoglycemic [OB-NG] and six obese with type 2 diabetes [OB-T2D]) were included in the study. Gene and protein expression levels of STX8 and GLUT4 were analyzed in visceral adipose tissue (VAT).METHODSWith this purpose, 21 subjects (seven lean [LN], eight obese normoglycemic [OB-NG] and six obese with type 2 diabetes [OB-T2D]) were included in the study. Gene and protein expression levels of STX8 and GLUT4 were analyzed in visceral adipose tissue (VAT).mRNA (p = 0.008) and protein (p <0.001) expression levels of STX8 were significantly increased in VAT of OB-T2D patients. Moreover, gene expression levels of SLC2A4 (GLUT4) were downregulated (p = 0.002) in VAT of obese patients. We found that STX8 was positively correlated (p <0.05) with fasting glucose concentrations, plasma glucose 2 h after an OGTT and C-reactive protein. Interestingly, the expression of STX8 was negatively correlated (p <0.05) with the expression of SLC2A4 in VAT.RESULTSmRNA (p = 0.008) and protein (p <0.001) expression levels of STX8 were significantly increased in VAT of OB-T2D patients. Moreover, gene expression levels of SLC2A4 (GLUT4) were downregulated (p = 0.002) in VAT of obese patients. We found that STX8 was positively correlated (p <0.05) with fasting glucose concentrations, plasma glucose 2 h after an OGTT and C-reactive protein. Interestingly, the expression of STX8 was negatively correlated (p <0.05) with the expression of SLC2A4 in VAT.Increased STX8 expression in VAT appears to be associated with the presence of T2D in obese patients through a mechanism that may involve GLUT4.CONCLUSIONSIncreased STX8 expression in VAT appears to be associated with the presence of T2D in obese patients through a mechanism that may involve GLUT4. Background and Aims Obesity is associated with increased adipose tissue inflammation as well as with the development of type 2 diabetes (T2D). Syntaxin 8 (STX8) is a protein required for the transport of endosomes. In this study we analyzed the relationship of STX8 with the presence of T2D in the context of obesity. Methods With this purpose, 21 subjects (seven lean [LN], eight obese normoglycemic [OB-NG] and six obese with type 2 diabetes [OB-T2D]) were included in the study. Gene and protein expression levels of STX8 and GLUT4 were analyzed in visceral adipose tissue (VAT). Results mRNA ( p = 0.008) and protein ( p <0.001) expression levels of STX8 were significantly increased in VAT of OB-T2D patients. Moreover, gene expression levels of SLC2A4 (GLUT4) were downregulated ( p = 0.002) in VAT of obese patients. We found that STX8 was positively correlated ( p <0.05) with fasting glucose concentrations, plasma glucose 2 h after an OGTT and C-reactive protein. Interestingly, the expression of STX8 was negatively correlated ( p <0.05) with the expression of SLC2A4 in VAT. Conclusions Increased STX8 expression in VAT appears to be associated with the presence of T2D in obese patients through a mechanism that may involve GLUT4. Obesity is associated with increased adipose tissue inflammation as well as with the development of type 2 diabetes (T2D). Syntaxin 8 (STX8) is a protein required for the transport of endosomes. In this study we analyzed the relationship of STX8 with the presence of T2D in the context of obesity. With this purpose, 21 subjects (seven lean [LN], eight obese normoglycemic [OB-NG] and six obese with type 2 diabetes [OB-T2D]) were included in the study. Gene and protein expression levels of STX8 and GLUT4 were analyzed in visceral adipose tissue (VAT). mRNA (p = 0.008) and protein (p <0.001) expression levels of STX8 were significantly increased in VAT of OB-T2D patients. Moreover, gene expression levels of SLC2A4 (GLUT4) were downregulated (p = 0.002) in VAT of obese patients. We found that STX8 was positively correlated (p <0.05) with fasting glucose concentrations, plasma glucose 2 h after an OGTT and C-reactive protein. Interestingly, the expression of STX8 was negatively correlated (p <0.05) with the expression of SLC2A4 in VAT. Increased STX8 expression in VAT appears to be associated with the presence of T2D in obese patients through a mechanism that may involve GLUT4. |
Author | Lancha, Andoni Gómez-Ambrosi, Javier Rodríguez, Amaia Moncada, Rafael Salvador, Javier Frühbeck, Gema López-Garrido, Santiago Gil, María J. Catalán, Victoria Silva, Camilo Ramírez, Beatriz Valentí, Víctor |
Author_xml | – sequence: 1 givenname: Andoni surname: Lancha fullname: Lancha, Andoni organization: Metabolic Research Laboratory, Clínica Universidad de Navarra, Pamplona, Spain – sequence: 2 givenname: Santiago surname: López-Garrido fullname: López-Garrido, Santiago organization: Metabolic Research Laboratory, Clínica Universidad de Navarra, Pamplona, Spain – sequence: 3 givenname: Amaia surname: Rodríguez fullname: Rodríguez, Amaia organization: Metabolic Research Laboratory, Clínica Universidad de Navarra, Pamplona, Spain – sequence: 4 givenname: Victoria surname: Catalán fullname: Catalán, Victoria organization: Metabolic Research Laboratory, Clínica Universidad de Navarra, Pamplona, Spain – sequence: 5 givenname: Beatriz surname: Ramírez fullname: Ramírez, Beatriz organization: Metabolic Research Laboratory, Clínica Universidad de Navarra, Pamplona, Spain – sequence: 6 givenname: Víctor surname: Valentí fullname: Valentí, Víctor organization: CIBER Fisiopatología de la Obesidad y Nutrición (CIBERobn), Instituto de Salud Carlos III, Pamplona, Spain – sequence: 7 givenname: Rafael surname: Moncada fullname: Moncada, Rafael organization: Obesity and Adipobiology Group, Instituto de Investigación Sanitaria de Navarra, Pamplona, Spain – sequence: 8 givenname: Camilo surname: Silva fullname: Silva, Camilo organization: CIBER Fisiopatología de la Obesidad y Nutrición (CIBERobn), Instituto de Salud Carlos III, Pamplona, Spain – sequence: 9 givenname: María J. surname: Gil fullname: Gil, María J. organization: CIBER Fisiopatología de la Obesidad y Nutrición (CIBERobn), Instituto de Salud Carlos III, Pamplona, Spain – sequence: 10 givenname: Javier surname: Salvador fullname: Salvador, Javier organization: CIBER Fisiopatología de la Obesidad y Nutrición (CIBERobn), Instituto de Salud Carlos III, Pamplona, Spain – sequence: 11 givenname: Gema surname: Frühbeck fullname: Frühbeck, Gema organization: Metabolic Research Laboratory, Clínica Universidad de Navarra, Pamplona, Spain – sequence: 12 givenname: Javier surname: Gómez-Ambrosi fullname: Gómez-Ambrosi, Javier email: jagomez@unav.es organization: Metabolic Research Laboratory, Clínica Universidad de Navarra, Pamplona, Spain |
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Keywords | Type 2 diabetes Obesity Visceral adipose tissue GLUT4 Syntaxin 8 |
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Snippet | Obesity is associated with increased adipose tissue inflammation as well as with the development of type 2 diabetes (T2D). Syntaxin 8 (STX8) is a protein... Background and Aims Obesity is associated with increased adipose tissue inflammation as well as with the development of type 2 diabetes (T2D). Syntaxin 8... |
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SubjectTerms | Adult Biomarkers - metabolism Blood Glucose - analysis C-Reactive Protein - metabolism Diabetes Mellitus, Type 2 - pathology Female Gene Expression Glucose Transporter Type 4 - biosynthesis GLUT4 Humans Inflammation - immunology Insulin Resistance - genetics Internal Medicine Intra-Abdominal Fat - metabolism Male Middle Aged Obesity Obesity - metabolism Qa-SNARE Proteins - biosynthesis RNA, Messenger - genetics Syntaxin 8 Type 2 diabetes Visceral adipose tissue |
Title | Expression of Syntaxin 8 in Visceral Adipose Tissue Is Increased in Obese Patients with Type 2 Diabetes and Related to Markers of Insulin Resistance and Inflammation |
URI | https://www.clinicalkey.com/#!/content/1-s2.0-S0188440914002811 https://www.clinicalkey.es/playcontent/1-s2.0-S0188440914002811 https://dx.doi.org/10.1016/j.arcmed.2014.12.003 https://www.ncbi.nlm.nih.gov/pubmed/25523146 https://www.proquest.com/docview/1669836031 |
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