author_facet Wang, Xinwen
LeMaire, Scott A.
Chen, Li
Shen, Ying H.
Gan, Yehua
Bartsch, Heather
Carter, Stacey A.
Utama, Budi
Ou, Hesheng
Coselli, Joseph S.
Wang, Xing Li
Wang, Xinwen
LeMaire, Scott A.
Chen, Li
Shen, Ying H.
Gan, Yehua
Bartsch, Heather
Carter, Stacey A.
Utama, Budi
Ou, Hesheng
Coselli, Joseph S.
Wang, Xing Li
author Wang, Xinwen
LeMaire, Scott A.
Chen, Li
Shen, Ying H.
Gan, Yehua
Bartsch, Heather
Carter, Stacey A.
Utama, Budi
Ou, Hesheng
Coselli, Joseph S.
Wang, Xing Li
spellingShingle Wang, Xinwen
LeMaire, Scott A.
Chen, Li
Shen, Ying H.
Gan, Yehua
Bartsch, Heather
Carter, Stacey A.
Utama, Budi
Ou, Hesheng
Coselli, Joseph S.
Wang, Xing Li
Circulation
Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection
Physiology (medical)
Cardiology and Cardiovascular Medicine
author_sort wang, xinwen
spelling Wang, Xinwen LeMaire, Scott A. Chen, Li Shen, Ying H. Gan, Yehua Bartsch, Heather Carter, Stacey A. Utama, Budi Ou, Hesheng Coselli, Joseph S. Wang, Xing Li 0009-7322 1524-4539 Ovid Technologies (Wolters Kluwer Health) Physiology (medical) Cardiology and Cardiovascular Medicine http://dx.doi.org/10.1161/circulationaha.105.000240 <jats:p> <jats:bold> <jats:italic>Background—</jats:italic> </jats:bold> Thoracic aortic dissection (TAD) is characterized by dysregulated extracellular matrix. Little is known about the alterations of collagen and stimulators of collagen synthesis, eg, connective tissue growth factor (CTGF), in patients with TAD. In this study, we examined their roles in TAD. </jats:p> <jats:p> <jats:bold> <jats:italic>Methods and Results—</jats:italic> </jats:bold> Surgical specimens of the aortic wall of TAD patients (n=10) and controls (n=10) were tested for collagen types I and III and CTGF expression. When compared with controls, protein levels of type I and III collagen and CTGF were significantly increased by 3.2-, 3.7-, and 5.3-fold, respectively ( <jats:italic>P</jats:italic> &lt;0.05 for all). Similar patterns were shown in mRNA levels of type Iα and Iα2 collagen and CTGF. Using immunohistochemistry and trichrome staining, we also observed elevated levels of collagen in the aortic media and adventitia. Treatment with recombinant human CTGF increased collagen synthesis in cultured aortic smooth muscle cells in a dose- and time-dependent fashion, in which expression of collagens increased from 506±108 counts per minute to 2764±240 cpm by 50 ng/mL CTGF, and from 30±43 cpm to 429±102 cpm at 48 hours. </jats:p> <jats:p> <jats:bold> <jats:italic>Conclusions—</jats:italic> </jats:bold> TAD patients exhibited significantly increased expression of aortic collagen types I and III as well as CTGF, which is likely to be responsible for the compromised aortic distensibility and systemic compliance. Because CTGF can increase collagen expression, CTGF may be a new target molecule in the pathogenesis and progression of TAD. </jats:p> Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection Circulation
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title Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection
title_unstemmed Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection
title_full Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection
title_fullStr Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection
title_full_unstemmed Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection
title_short Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection
title_sort increased collagen deposition and elevated expression of connective tissue growth factor in human thoracic aortic dissection
topic Physiology (medical)
Cardiology and Cardiovascular Medicine
url http://dx.doi.org/10.1161/circulationaha.105.000240
publishDate 2006
physical
description <jats:p> <jats:bold> <jats:italic>Background—</jats:italic> </jats:bold> Thoracic aortic dissection (TAD) is characterized by dysregulated extracellular matrix. Little is known about the alterations of collagen and stimulators of collagen synthesis, eg, connective tissue growth factor (CTGF), in patients with TAD. In this study, we examined their roles in TAD. </jats:p> <jats:p> <jats:bold> <jats:italic>Methods and Results—</jats:italic> </jats:bold> Surgical specimens of the aortic wall of TAD patients (n=10) and controls (n=10) were tested for collagen types I and III and CTGF expression. When compared with controls, protein levels of type I and III collagen and CTGF were significantly increased by 3.2-, 3.7-, and 5.3-fold, respectively ( <jats:italic>P</jats:italic> &lt;0.05 for all). Similar patterns were shown in mRNA levels of type Iα and Iα2 collagen and CTGF. Using immunohistochemistry and trichrome staining, we also observed elevated levels of collagen in the aortic media and adventitia. Treatment with recombinant human CTGF increased collagen synthesis in cultured aortic smooth muscle cells in a dose- and time-dependent fashion, in which expression of collagens increased from 506±108 counts per minute to 2764±240 cpm by 50 ng/mL CTGF, and from 30±43 cpm to 429±102 cpm at 48 hours. </jats:p> <jats:p> <jats:bold> <jats:italic>Conclusions—</jats:italic> </jats:bold> TAD patients exhibited significantly increased expression of aortic collagen types I and III as well as CTGF, which is likely to be responsible for the compromised aortic distensibility and systemic compliance. Because CTGF can increase collagen expression, CTGF may be a new target molecule in the pathogenesis and progression of TAD. </jats:p>
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author Wang, Xinwen, LeMaire, Scott A., Chen, Li, Shen, Ying H., Gan, Yehua, Bartsch, Heather, Carter, Stacey A., Utama, Budi, Ou, Hesheng, Coselli, Joseph S., Wang, Xing Li
author_facet Wang, Xinwen, LeMaire, Scott A., Chen, Li, Shen, Ying H., Gan, Yehua, Bartsch, Heather, Carter, Stacey A., Utama, Budi, Ou, Hesheng, Coselli, Joseph S., Wang, Xing Li, Wang, Xinwen, LeMaire, Scott A., Chen, Li, Shen, Ying H., Gan, Yehua, Bartsch, Heather, Carter, Stacey A., Utama, Budi, Ou, Hesheng, Coselli, Joseph S., Wang, Xing Li
author_sort wang, xinwen
container_issue 1_supplement
container_start_page 0
container_title Circulation
container_volume 114
description <jats:p> <jats:bold> <jats:italic>Background—</jats:italic> </jats:bold> Thoracic aortic dissection (TAD) is characterized by dysregulated extracellular matrix. Little is known about the alterations of collagen and stimulators of collagen synthesis, eg, connective tissue growth factor (CTGF), in patients with TAD. In this study, we examined their roles in TAD. </jats:p> <jats:p> <jats:bold> <jats:italic>Methods and Results—</jats:italic> </jats:bold> Surgical specimens of the aortic wall of TAD patients (n=10) and controls (n=10) were tested for collagen types I and III and CTGF expression. When compared with controls, protein levels of type I and III collagen and CTGF were significantly increased by 3.2-, 3.7-, and 5.3-fold, respectively ( <jats:italic>P</jats:italic> &lt;0.05 for all). Similar patterns were shown in mRNA levels of type Iα and Iα2 collagen and CTGF. Using immunohistochemistry and trichrome staining, we also observed elevated levels of collagen in the aortic media and adventitia. Treatment with recombinant human CTGF increased collagen synthesis in cultured aortic smooth muscle cells in a dose- and time-dependent fashion, in which expression of collagens increased from 506±108 counts per minute to 2764±240 cpm by 50 ng/mL CTGF, and from 30±43 cpm to 429±102 cpm at 48 hours. </jats:p> <jats:p> <jats:bold> <jats:italic>Conclusions—</jats:italic> </jats:bold> TAD patients exhibited significantly increased expression of aortic collagen types I and III as well as CTGF, which is likely to be responsible for the compromised aortic distensibility and systemic compliance. Because CTGF can increase collagen expression, CTGF may be a new target molecule in the pathogenesis and progression of TAD. </jats:p>
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spelling Wang, Xinwen LeMaire, Scott A. Chen, Li Shen, Ying H. Gan, Yehua Bartsch, Heather Carter, Stacey A. Utama, Budi Ou, Hesheng Coselli, Joseph S. Wang, Xing Li 0009-7322 1524-4539 Ovid Technologies (Wolters Kluwer Health) Physiology (medical) Cardiology and Cardiovascular Medicine http://dx.doi.org/10.1161/circulationaha.105.000240 <jats:p> <jats:bold> <jats:italic>Background—</jats:italic> </jats:bold> Thoracic aortic dissection (TAD) is characterized by dysregulated extracellular matrix. Little is known about the alterations of collagen and stimulators of collagen synthesis, eg, connective tissue growth factor (CTGF), in patients with TAD. In this study, we examined their roles in TAD. </jats:p> <jats:p> <jats:bold> <jats:italic>Methods and Results—</jats:italic> </jats:bold> Surgical specimens of the aortic wall of TAD patients (n=10) and controls (n=10) were tested for collagen types I and III and CTGF expression. When compared with controls, protein levels of type I and III collagen and CTGF were significantly increased by 3.2-, 3.7-, and 5.3-fold, respectively ( <jats:italic>P</jats:italic> &lt;0.05 for all). Similar patterns were shown in mRNA levels of type Iα and Iα2 collagen and CTGF. Using immunohistochemistry and trichrome staining, we also observed elevated levels of collagen in the aortic media and adventitia. Treatment with recombinant human CTGF increased collagen synthesis in cultured aortic smooth muscle cells in a dose- and time-dependent fashion, in which expression of collagens increased from 506±108 counts per minute to 2764±240 cpm by 50 ng/mL CTGF, and from 30±43 cpm to 429±102 cpm at 48 hours. </jats:p> <jats:p> <jats:bold> <jats:italic>Conclusions—</jats:italic> </jats:bold> TAD patients exhibited significantly increased expression of aortic collagen types I and III as well as CTGF, which is likely to be responsible for the compromised aortic distensibility and systemic compliance. Because CTGF can increase collagen expression, CTGF may be a new target molecule in the pathogenesis and progression of TAD. </jats:p> Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection Circulation
spellingShingle Wang, Xinwen, LeMaire, Scott A., Chen, Li, Shen, Ying H., Gan, Yehua, Bartsch, Heather, Carter, Stacey A., Utama, Budi, Ou, Hesheng, Coselli, Joseph S., Wang, Xing Li, Circulation, Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection, Physiology (medical), Cardiology and Cardiovascular Medicine
title Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection
title_full Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection
title_fullStr Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection
title_full_unstemmed Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection
title_short Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection
title_sort increased collagen deposition and elevated expression of connective tissue growth factor in human thoracic aortic dissection
title_unstemmed Increased Collagen Deposition and Elevated Expression of Connective Tissue Growth Factor in Human Thoracic Aortic Dissection
topic Physiology (medical), Cardiology and Cardiovascular Medicine
url http://dx.doi.org/10.1161/circulationaha.105.000240