Source:http://linkedlifedata.com/resource/pubmed/id/19775691
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2010-3-1
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pubmed:abstractText |
Cathepsin K (catK), a lysosomal cysteine protease, exerts strong elastinolytic and collagenolytic activity and is implicated in a range of pathological disorders including cardiovascular disease. CatK expression was found to be elevated in human aortic aneurysm pointing to a role in this vasculopathy. In the angiotensin II (Ang II)-induced mouse model for aneurysm formation, catK, S and C expression was strongly upregulated. Therefore, we investigated the effect of catK deficiency on Ang II-induced aneurysm formation in the abdominal aorta of apoE-/- mice. Contrary to our expectations, catK deficiency did not protect against aneurysm formation, nor did it affect medial elastin breaks. Proteolytic activity in abdominal aortic lysates were comparable between apoE-/- and catK-//-apoE-/- mice. Adventitial presence of catS- and catC-expressing cells was significantly increased in catK-/-//apoE-/- versus apoE-/- mice, which might have compensated for the deficiency of catK-derived proteolysis in the aneurysm tissue of catK deficient apoE-/- mice. Circulating granulocytes and activated T cell numbers were significantly increased in Ang II-infused catK-/-//apoE-/- mice, which is consistent with the borderline significant increase in adventitial leukocyte content in catK-/-//apoE-/- compared to apoE-/- mice. Strikingly, despite unchanged proteolytic activity in AAA lesions, collagen content in the aneurysm was significantly increased in catK-//-apoE-/- mice. In conclusion, while catK deficiency has major impact on various vasculopathies, it did not affect murine aneurysm formation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Angiotensin II,
http://linkedlifedata.com/resource/pubmed/chemical/Apolipoproteins E,
http://linkedlifedata.com/resource/pubmed/chemical/Cathepsin C,
http://linkedlifedata.com/resource/pubmed/chemical/Cathepsin K,
http://linkedlifedata.com/resource/pubmed/chemical/Cathepsins,
http://linkedlifedata.com/resource/pubmed/chemical/Collagen,
http://linkedlifedata.com/resource/pubmed/chemical/Ctsc protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Ctsk protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/cathepsin S
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1879-1484
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pubmed:author |
pubmed-author:BeckersLindaL,
pubmed-author:BiessenErik A LEA,
pubmed-author:CleutjensKittyK,
pubmed-author:DaemenMat J A PMJ,
pubmed-author:HeenemanSylviaS,
pubmed-author:HeríasM VerónicaMV,
pubmed-author:LutgensEstherE,
pubmed-author:LutgensSuzanne P MSP,
pubmed-author:ParkA YAY,
pubmed-author:SaftigPaulP,
pubmed-author:WijnandsErwinE
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pubmed:issnType |
Electronic
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pubmed:volume |
209
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
96-103
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pubmed:meshHeading |
pubmed-meshheading:19775691-Angiotensin II,
pubmed-meshheading:19775691-Animals,
pubmed-meshheading:19775691-Aortic Aneurysm, Abdominal,
pubmed-meshheading:19775691-Apolipoproteins E,
pubmed-meshheading:19775691-Cathepsin C,
pubmed-meshheading:19775691-Cathepsin K,
pubmed-meshheading:19775691-Cathepsins,
pubmed-meshheading:19775691-Collagen,
pubmed-meshheading:19775691-Granulocytes,
pubmed-meshheading:19775691-Lymphocyte Count,
pubmed-meshheading:19775691-Macrophages,
pubmed-meshheading:19775691-Mice,
pubmed-meshheading:19775691-Mice, Inbred C57BL,
pubmed-meshheading:19775691-Mice, Mutant Strains,
pubmed-meshheading:19775691-T-Lymphocytes
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pubmed:year |
2010
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pubmed:articleTitle |
Cathepsin K gene disruption does not affect murine aneurysm formation.
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pubmed:affiliation |
Experimental Vascular Pathology Group, Department of Pathology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center, P. Debyelaan 25, Maastricht, The Netherlands.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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