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Inhibition of Src Kinase Blocks High Glucose–Induced EGFR Transactivation and Collagen Synthesis in Mesangial Cells and Prevents Diabetic Nephropathy in Mice

Chronic exposure to high glucose leads to diabetic nephropathy characterized by increased mesangial matrix protein (e.g., collagen) accumulation. Altered cell signaling and gene expression accompanied by oxidative stress have been documented. The contribution of the tyrosine kinase, c-Src (Src), whi...

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Autores principales: Taniguchi, Kanta, Xia, Ling, Goldberg, Howard J., Lee, Ken W.K., Shah, Anu, Stavar, Laura, Masson, Elodie A.Y., Momen, Abdul, Shikatani, Eric A., John, Rohan, Husain, Mansoor, Fantus, I. George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3806624/
https://www.ncbi.nlm.nih.gov/pubmed/23942551
http://dx.doi.org/10.2337/db12-1010
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author Taniguchi, Kanta
Xia, Ling
Goldberg, Howard J.
Lee, Ken W.K.
Shah, Anu
Stavar, Laura
Masson, Elodie A.Y.
Momen, Abdul
Shikatani, Eric A.
John, Rohan
Husain, Mansoor
Fantus, I. George
author_facet Taniguchi, Kanta
Xia, Ling
Goldberg, Howard J.
Lee, Ken W.K.
Shah, Anu
Stavar, Laura
Masson, Elodie A.Y.
Momen, Abdul
Shikatani, Eric A.
John, Rohan
Husain, Mansoor
Fantus, I. George
author_sort Taniguchi, Kanta
collection PubMed
description Chronic exposure to high glucose leads to diabetic nephropathy characterized by increased mesangial matrix protein (e.g., collagen) accumulation. Altered cell signaling and gene expression accompanied by oxidative stress have been documented. The contribution of the tyrosine kinase, c-Src (Src), which is sensitive to oxidative stress, was examined. Cultured rat mesangial cells were exposed to high glucose (25 mmol/L) in the presence and absence of Src inhibitors (PP2, SU6656), Src small interfering RNA (siRNA), and the tumor necrosis factor-α–converting enzyme (TACE) inhibitor, TAPI-2. Src was investigated in vivo by administration of PP2 to streptozotocin (STZ)-induced diabetic DBA2/J mice. High glucose stimulated Src, TACE, epidermal growth factor receptor (EGFR), mitogen-activated protein kinases (MAPKs), extracellular signal–regulated kinase (ERK1/2, p38), and collagen IV accumulation in mesangial cells. PP2 and SU6656 blocked high glucose–stimulated phosphorylation of Src Tyr-416, EGFR, and MAPKs. These inhibitors and Src knockdown by siRNA, as well as TAPI-2, also abrogated high glucose–induced phosphorylation of these targets and collagen IV accumulation. In STZ-diabetic mice, albuminuria, increased Src pTyr-416, TACE activation, ERK and EGFR phosphorylation, glomerular collagen accumulation, and podocyte loss were inhibited by PP2. These data indicate a role for Src in a high glucose-Src-TACE-heparin-binding epidermal growth factor-EGFR-MAPK–signaling pathway to collagen accumulation. Thus, Src may provide a novel therapeutic target for diabetic nephropathy.
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spelling pubmed-38066242014-11-01 Inhibition of Src Kinase Blocks High Glucose–Induced EGFR Transactivation and Collagen Synthesis in Mesangial Cells and Prevents Diabetic Nephropathy in Mice Taniguchi, Kanta Xia, Ling Goldberg, Howard J. Lee, Ken W.K. Shah, Anu Stavar, Laura Masson, Elodie A.Y. Momen, Abdul Shikatani, Eric A. John, Rohan Husain, Mansoor Fantus, I. George Diabetes Original Research Chronic exposure to high glucose leads to diabetic nephropathy characterized by increased mesangial matrix protein (e.g., collagen) accumulation. Altered cell signaling and gene expression accompanied by oxidative stress have been documented. The contribution of the tyrosine kinase, c-Src (Src), which is sensitive to oxidative stress, was examined. Cultured rat mesangial cells were exposed to high glucose (25 mmol/L) in the presence and absence of Src inhibitors (PP2, SU6656), Src small interfering RNA (siRNA), and the tumor necrosis factor-α–converting enzyme (TACE) inhibitor, TAPI-2. Src was investigated in vivo by administration of PP2 to streptozotocin (STZ)-induced diabetic DBA2/J mice. High glucose stimulated Src, TACE, epidermal growth factor receptor (EGFR), mitogen-activated protein kinases (MAPKs), extracellular signal–regulated kinase (ERK1/2, p38), and collagen IV accumulation in mesangial cells. PP2 and SU6656 blocked high glucose–stimulated phosphorylation of Src Tyr-416, EGFR, and MAPKs. These inhibitors and Src knockdown by siRNA, as well as TAPI-2, also abrogated high glucose–induced phosphorylation of these targets and collagen IV accumulation. In STZ-diabetic mice, albuminuria, increased Src pTyr-416, TACE activation, ERK and EGFR phosphorylation, glomerular collagen accumulation, and podocyte loss were inhibited by PP2. These data indicate a role for Src in a high glucose-Src-TACE-heparin-binding epidermal growth factor-EGFR-MAPK–signaling pathway to collagen accumulation. Thus, Src may provide a novel therapeutic target for diabetic nephropathy. American Diabetes Association 2013-11 2013-10-18 /pmc/articles/PMC3806624/ /pubmed/23942551 http://dx.doi.org/10.2337/db12-1010 Text en © 2013 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
Taniguchi, Kanta
Xia, Ling
Goldberg, Howard J.
Lee, Ken W.K.
Shah, Anu
Stavar, Laura
Masson, Elodie A.Y.
Momen, Abdul
Shikatani, Eric A.
John, Rohan
Husain, Mansoor
Fantus, I. George
Inhibition of Src Kinase Blocks High Glucose–Induced EGFR Transactivation and Collagen Synthesis in Mesangial Cells and Prevents Diabetic Nephropathy in Mice
title Inhibition of Src Kinase Blocks High Glucose–Induced EGFR Transactivation and Collagen Synthesis in Mesangial Cells and Prevents Diabetic Nephropathy in Mice
title_full Inhibition of Src Kinase Blocks High Glucose–Induced EGFR Transactivation and Collagen Synthesis in Mesangial Cells and Prevents Diabetic Nephropathy in Mice
title_fullStr Inhibition of Src Kinase Blocks High Glucose–Induced EGFR Transactivation and Collagen Synthesis in Mesangial Cells and Prevents Diabetic Nephropathy in Mice
title_full_unstemmed Inhibition of Src Kinase Blocks High Glucose–Induced EGFR Transactivation and Collagen Synthesis in Mesangial Cells and Prevents Diabetic Nephropathy in Mice
title_short Inhibition of Src Kinase Blocks High Glucose–Induced EGFR Transactivation and Collagen Synthesis in Mesangial Cells and Prevents Diabetic Nephropathy in Mice
title_sort inhibition of src kinase blocks high glucose–induced egfr transactivation and collagen synthesis in mesangial cells and prevents diabetic nephropathy in mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3806624/
https://www.ncbi.nlm.nih.gov/pubmed/23942551
http://dx.doi.org/10.2337/db12-1010
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