62 research outputs found

    Cartilage-Specific Over-Expression of CCN Family Member 2/Connective Tissue Growth Factor (CCN2/CTGF) Stimulates Insulin-Like Growth Factor Expression and Bone Growth

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    Previously we showed that CCN family member 2/connective tissue growth factor (CCN2) promotes the proliferation, differentiation, and maturation of growth cartilage cells in vitro. To elucidate the specific role and molecular mechanism of CCN2 in cartilage development in vivo, in the present study we generated transgenic mice overexpressing CCN2 and analyzed them with respect to cartilage and bone development. Transgenic mice were generated expressing a ccn2/lacZ fusion gene in cartilage under the control of the 6 kb-Col2a1-enhancer/promoter. Changes in cartilage and bone development were analyzed histologically and immunohistologically and also by micro CT. Primary chondrocytes as well as limb bud mesenchymal cells were cultured and analyzed for changes in expression of cartilage-related genes, and non-transgenic chondrocytes were treated in culture with recombinant CCN2. Newborn transgenic mice showed extended length of their long bones, increased content of proteoglycans and collagen II accumulation. Micro-CT analysis of transgenic bones indicated increases in bone thickness and mineral density. Chondrocyte proliferation was enhanced in the transgenic cartilage. In in vitro short-term cultures of transgenic chondrocytes, the expression of col2a1, aggrecan and ccn2 genes was substantially enhanced; and in long-term cultures the expression levels of these genes were further enhanced. Also, in vitro chondrogenesis was strongly enhanced. IGF-I and IGF-II mRNA levels were elevated in transgenic chondrocytes, and treatment of non-transgenic chondrocytes with recombinant CCN2 stimulated the expression of these mRNA. The addition of CCN2 to non-transgenic chondrocytes induced the phosphorylation of IGFR, and ccn2-overexpressing chondrocytes showed enhanced phosphorylation of IGFR. Our data indicates that the observed effects of CCN2 may be mediated in part by CCN2-induced overexpression of IGF-I and IGF-II. These findings indicate that CCN2-overexpression in transgenic mice accelerated the endochondral ossification processes, resulting in increased length of their long bones. Our results also indicate the possible involvement of locally enhanced IGF-I or IGF-II in this extended bone growth

    The interstitium in cardiac repair: role of the immune-stromal cell interplay

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    Cardiac regeneration, that is, restoration of the original structure and function in a damaged heart, differs from tissue repair, in which collagen deposition and scar formation often lead to functional impairment. In both scenarios, the early-onset inflammatory response is essential to clear damaged cardiac cells and initiate organ repair, but the quality and extent of the immune response vary. Immune cells embedded in the damaged heart tissue sense and modulate inflammation through a dynamic interplay with stromal cells in the cardiac interstitium, which either leads to recapitulation of cardiac morphology by rebuilding functional scaffolds to support muscle regrowth in regenerative organisms or fails to resolve the inflammatory response and produces fibrotic scar tissue in adult mammals. Current investigation into the mechanistic basis of homeostasis and restoration of cardiac function has increasingly shifted focus away from stem cell-mediated cardiac repair towards a dynamic interplay of cells composing the less-studied interstitial compartment of the heart, offering unexpected insights into the immunoregulatory functions of cardiac interstitial components and the complex network of cell interactions that must be considered for clinical intervention in heart diseases

    Right ventricular mechanics in hypertrophic cardiomyopathy using feature tracking

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    Imaging techniques in transcatheter aortic valve replacement

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    Robert A Quaife, Jennifer Dorosz, John C Messenger, Ernesto E Salcedo Division of Cardiology, University of Colorado, Aurora, CO, USA Abstract: Calcific aortic stenosis is now understood as a complex valvular degenerative process sharing many risk factors with atherosclerosis. Once patients develop symptomatic calcific aortic stenosis, the only effective treatment is aortic valve replacement. In the past decade, transcatheter aortic valve replacement (TAVR) has been developed as an alternative to surgery to treat severe calcific aortic stenosis. Cardiac imaging plays a pivotal role in the contemporary management of patients with calcific aortic stenosis, and particularly in patients being considered for TAVR, who demand detailed imaging of the aortic valve apparatus. In this review, we highlight the role of cardiac imaging for patient selection, procedural guidance, and evaluation of results of TAVR. Keywords: aortic stenosis, cardiovascular imaging, transcutaneous aortic valve replacemen

    Are inventory based and remotely sensed above-ground biomass estimates consistent?

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    Carbon emissions resulting from deforestation and forest degradation are poorly known at local, national and global scales. In part, this lack of knowledge results from uncertain above-ground biomass estimates. It is generally assumed that using more sophisticated methods of estimating above-ground biomass, which make use of remote sensing, will improve accuracy. We examine this assumption by calculating, and then comparing, above-ground biomass area density (AGBD) estimates from studies with differing levels of methodological sophistication. We consider estimates based on information from nine different studies at the scale of Africa, Mozambique and a 1160 km2 study area within Mozambique. The true AGBD is not known for these scales and so accuracy cannot be determined. Instead we consider the overall precision of estimates by grouping different studies. Since an the accuracy of an estimate cannot exceed its precision, this approach provides an upper limit on the overall accuracy of the group. This reveals poor precision at all scales, even between studies that are based on conceptually similar approaches. Mean AGBD estimates for Africa vary from 19.9 to 44.3 Mg ha−1, for Mozambique from 12.7 to 68.3 Mg ha−1, and for the 1160 km2 study area estimates range from 35.6 to 102.4 Mg ha−1. The original uncertainty estimates for each study, when available, are generally small in comparison with the differences between mean biomass estimates of different studies. We find that increasing methodological sophistication does not appear to result in improved precision of AGBD estimates, and moreover, inadequate estimates of uncertainty obscure any improvements in accuracy. Therefore, despite the clear advantages of remote sensing, there is a need to improve remotely sensed AGBD estimates if they are to provide accurate information on above-ground biomass. In particular, more robust and comprehensive uncertainty estimates are needed.Publisher PDFPeer reviewe
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