Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2010-4-27
pubmed:abstractText
Although matrix metalloproteinase (MMPs) and tissue inhibitor of metalloproteinase (TIMPs) play a vital role in tumour angiogenesis and TIMP-3 caused apoptosis, their role in cardiac angiogenesis is unknown. Interestingly, a disruption of co-ordinated cardiac hypertrophy and angiogenesis contributed to the transition to heart failure, however, the proteolytic and anti-angiogenic mechanisms of transition from compensatory hypertrophy to decompensatory heart failure were unclear. We hypothesized that after an aortic stenosis MMP-2 released angiogenic factors during compensatory hypertrophy and MMP-9/TIMP-3 released anti-angiogenic factors causing decompensatory heart failure. To verify this hypothesis, wild type (WT) mice were studied 3 and 8 weeks after aortic stenosis, created by banding the ascending aorta in WT and MMP-9-/- (MMP-9KO) mice. Cardiac function (echo, PV loops) was decreased at 8 weeks after stenosis. The levels of MMP-2 (western blot) increased at 3 weeks and returned to control level at 8 weeks, MMP-9 increased only at 8 weeks. TIMP-2 and -4 decreased at 3 and even more at 8 weeks. The angiogenic VEGF increased at 3 weeks and decreased at 8 weeks, the anti-angiogenic endostatin and angiostatin increased only at 8 weeks. CD-31 positive endothelial cells were more intensely labelled at 3 weeks than in sham operated or in 8 weeks banded mice. Vascularization, as estimated by x-ray angiography, was increased at 3 weeks and decreased at 8 weeks post-banding. Although the vast majority of studies were performed on control WT mice only, interestingly, MMP9-KO mice seemed to have increased vascular density 8 weeks after banding. These results suggested that there was increase in MMP-2, decrease in TIMP-2 and -4, increase in angiogenic factors and vascularization in compensatory hearts. However, in decompensatory hearts there was increase in MMP-9, TIMP-3, endostatin, angiostatin and vascular rarefaction.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-10189361, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-10206987, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-10716919, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-10880048, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-11034081, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-11169735, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-11257124, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-11514539, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-12029087, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-12154103, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-12354694, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-12524460, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-12928773, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-14743398, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-15096942, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-15650153, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-16075055, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-16126817, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-16369727, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-1689327, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-16989723, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-19074676, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-7731050, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-8013079, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-8320967, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-8485829, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-8841929, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-9008168, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-9034784, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-9062888, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-9502791, http://linkedlifedata.com/resource/pubmed/commentcorrection/20230216-9791730
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1744-4160
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
116
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
63-72
pubmed:dateRevised
2011-7-28
pubmed:meshHeading
pubmed-meshheading:20230216-Angiogenesis Inducing Agents, pubmed-meshheading:20230216-Animals, pubmed-meshheading:20230216-Aorta, pubmed-meshheading:20230216-Apoptosis, pubmed-meshheading:20230216-Blotting, Western, pubmed-meshheading:20230216-Cardiomegaly, pubmed-meshheading:20230216-Heart Failure, pubmed-meshheading:20230216-Hypertrophy, pubmed-meshheading:20230216-Matrix Metalloproteinase 2, pubmed-meshheading:20230216-Matrix Metalloproteinase 9, pubmed-meshheading:20230216-Matrix Metalloproteinases, pubmed-meshheading:20230216-Mice, pubmed-meshheading:20230216-Mice, Inbred C57BL, pubmed-meshheading:20230216-Mice, Knockout, pubmed-meshheading:20230216-Tissue Inhibitor of Metalloproteinase-2, pubmed-meshheading:20230216-Tissue Inhibitor of Metalloproteinase-3, pubmed-meshheading:20230216-X-Rays
pubmed:year
2010
pubmed:articleTitle
MMP-2/TIMP-2/TIMP-4 versus MMP-9/TIMP-3 in transition from compensatory hypertrophy and angiogenesis to decompensatory heart failure.
pubmed:affiliation
Department of Physiology and Biophysics, University of Louisville School of Medicine, 500 South Preston Street, Louisville, KY 40202, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural