Insulin promotes vascular smooth muscle cell proliferation and apoptosis via differential regulation of tumor necrosis factor‐related apoptosis‐inducing ligand

Background: Insulin regulates glucose homeostasis but can also promote vascular smooth muscle (VSMC) proliferation, important in atherogenesis. Recently, we showed that tumor necrosis factor‐related apoptosis‐inducing ligand (TRAIL) stimulates intimal thickening via accelerated growth of VSMCs. The...

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Main Authors: Harith, Hanis Hazeera, Di Bartolo, Belinda A., Cartland, Sian P., Genner, Scott, Kavurma, Mary M.
Format: Article
Language:English
Published: Wiley-Blackwell Publishing 2016
Subjects:
Online Access:http://psasir.upm.edu.my/id/eprint/54583/
http://psasir.upm.edu.my/id/eprint/54583/1/Insulin%20promotes%20vascular%20smooth%20muscle%20cell%20proliferation.pdf
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author Harith, Hanis Hazeera
Di Bartolo, Belinda A.
Cartland, Sian P.
Genner, Scott
Kavurma, Mary M.
author_facet Harith, Hanis Hazeera
Di Bartolo, Belinda A.
Cartland, Sian P.
Genner, Scott
Kavurma, Mary M.
author_sort Harith, Hanis Hazeera
building UPM Institutional Repository
collection Online Access
description Background: Insulin regulates glucose homeostasis but can also promote vascular smooth muscle (VSMC) proliferation, important in atherogenesis. Recently, we showed that tumor necrosis factor‐related apoptosis‐inducing ligand (TRAIL) stimulates intimal thickening via accelerated growth of VSMCs. The aim of the present study was to determine whether insulin‐induced effects on VSMCs occur via TRAIL. Methods: Expression of TRAIL and TRAIL receptor in response to insulin and glucose was determined by polymerase chain reaction. Transcriptional activity was assessed using wild‐type and site‐specific mutations of the TRAIL promoter. Chromatin immunoprecipitation studies were performed. VSMC proliferation and apoptosis was measured. Results: Insulin and glucose exposure to VSMC for 24 h stimulated TRAIL mRNA expression. This was also evident at the transcriptional level. Both insulin‐ and glucose‐inducible TRAIL transcriptional activity was blocked by dominant‐negative specificity protein‐1 (Sp1) overexpression. There are five functional Sp1‐binding elements (Sp1‐1, Sp1‐2, Sp‐5/6 and Sp1‐7) on the TRAIL promoter. Insulin required the Sp1‐1 and Sp1‐2 sites, but glucose needed all Sp1‐binding sites to induce transcription. Furthermore, insulin (but not glucose) was able to promote VSMC proliferation over time, associated with increased decoy receptor‐2 (DcR2) expression. In contrast, chronic 5‐day exposure of VSMC to 1 µg/mL insulin repressed TRAIL and DcR2 expression, and reduced Sp1 enrichment on the TRAIL promoter. This was associated with increased cell death. Conclusions: The findings of the present study provide a new mechanistic insight into how TRAIL is regulated by insulin. This may have significant implications at different stages of diabetes‐associated cardiovascular disease. Thus, TRAIL may offer a novel therapeutic solution to combat insulin‐induced vascular pathologies.
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spelling upm-545832018-04-02T05:22:04Z http://psasir.upm.edu.my/id/eprint/54583/ Insulin promotes vascular smooth muscle cell proliferation and apoptosis via differential regulation of tumor necrosis factor‐related apoptosis‐inducing ligand Harith, Hanis Hazeera Di Bartolo, Belinda A. Cartland, Sian P. Genner, Scott Kavurma, Mary M. Background: Insulin regulates glucose homeostasis but can also promote vascular smooth muscle (VSMC) proliferation, important in atherogenesis. Recently, we showed that tumor necrosis factor‐related apoptosis‐inducing ligand (TRAIL) stimulates intimal thickening via accelerated growth of VSMCs. The aim of the present study was to determine whether insulin‐induced effects on VSMCs occur via TRAIL. Methods: Expression of TRAIL and TRAIL receptor in response to insulin and glucose was determined by polymerase chain reaction. Transcriptional activity was assessed using wild‐type and site‐specific mutations of the TRAIL promoter. Chromatin immunoprecipitation studies were performed. VSMC proliferation and apoptosis was measured. Results: Insulin and glucose exposure to VSMC for 24 h stimulated TRAIL mRNA expression. This was also evident at the transcriptional level. Both insulin‐ and glucose‐inducible TRAIL transcriptional activity was blocked by dominant‐negative specificity protein‐1 (Sp1) overexpression. There are five functional Sp1‐binding elements (Sp1‐1, Sp1‐2, Sp‐5/6 and Sp1‐7) on the TRAIL promoter. Insulin required the Sp1‐1 and Sp1‐2 sites, but glucose needed all Sp1‐binding sites to induce transcription. Furthermore, insulin (but not glucose) was able to promote VSMC proliferation over time, associated with increased decoy receptor‐2 (DcR2) expression. In contrast, chronic 5‐day exposure of VSMC to 1 µg/mL insulin repressed TRAIL and DcR2 expression, and reduced Sp1 enrichment on the TRAIL promoter. This was associated with increased cell death. Conclusions: The findings of the present study provide a new mechanistic insight into how TRAIL is regulated by insulin. This may have significant implications at different stages of diabetes‐associated cardiovascular disease. Thus, TRAIL may offer a novel therapeutic solution to combat insulin‐induced vascular pathologies. Wiley-Blackwell Publishing 2016-07 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/54583/1/Insulin%20promotes%20vascular%20smooth%20muscle%20cell%20proliferation.pdf Harith, Hanis Hazeera and Di Bartolo, Belinda A. and Cartland, Sian P. and Genner, Scott and Kavurma, Mary M. (2016) Insulin promotes vascular smooth muscle cell proliferation and apoptosis via differential regulation of tumor necrosis factor‐related apoptosis‐inducing ligand. Journal of Diabetes Research, 8 (4). pp. 568-578. ISSN 1753-0393; ESSN: 1753-0407 https://onlinelibrary.wiley.com/doi/abs/10.1111/1753-0407.12339 Apoptosis; Gene expression; Insulin; Proliferation; Tumor necrosis factor-related apoptosis-inducing ligand 10.1111/1753-0407.12339
spellingShingle Apoptosis; Gene expression; Insulin; Proliferation; Tumor necrosis factor-related apoptosis-inducing ligand
Harith, Hanis Hazeera
Di Bartolo, Belinda A.
Cartland, Sian P.
Genner, Scott
Kavurma, Mary M.
Insulin promotes vascular smooth muscle cell proliferation and apoptosis via differential regulation of tumor necrosis factor‐related apoptosis‐inducing ligand
title Insulin promotes vascular smooth muscle cell proliferation and apoptosis via differential regulation of tumor necrosis factor‐related apoptosis‐inducing ligand
title_full Insulin promotes vascular smooth muscle cell proliferation and apoptosis via differential regulation of tumor necrosis factor‐related apoptosis‐inducing ligand
title_fullStr Insulin promotes vascular smooth muscle cell proliferation and apoptosis via differential regulation of tumor necrosis factor‐related apoptosis‐inducing ligand
title_full_unstemmed Insulin promotes vascular smooth muscle cell proliferation and apoptosis via differential regulation of tumor necrosis factor‐related apoptosis‐inducing ligand
title_short Insulin promotes vascular smooth muscle cell proliferation and apoptosis via differential regulation of tumor necrosis factor‐related apoptosis‐inducing ligand
title_sort insulin promotes vascular smooth muscle cell proliferation and apoptosis via differential regulation of tumor necrosis factor‐related apoptosis‐inducing ligand
topic Apoptosis; Gene expression; Insulin; Proliferation; Tumor necrosis factor-related apoptosis-inducing ligand
url http://psasir.upm.edu.my/id/eprint/54583/
http://psasir.upm.edu.my/id/eprint/54583/
http://psasir.upm.edu.my/id/eprint/54583/
http://psasir.upm.edu.my/id/eprint/54583/1/Insulin%20promotes%20vascular%20smooth%20muscle%20cell%20proliferation.pdf