Localized micro- and nano-scale remodelling in the diabetic aorta

被引:21
|
作者
Akhtar, R. [1 ]
Cruickshank, J. K. [2 ]
Zhao, X. [3 ]
Walton, L. A. [4 ]
Gardiner, N. J. [5 ]
Barrett, S. D. [6 ]
Graham, H. K. [7 ]
Derby, B. [3 ]
Sherratt, M. J. [7 ]
机构
[1] Univ Liverpool, Sch Engn, Ctr Mat & Struct, Liverpool L69 3GH, Merseyside, England
[2] Kings Coll London, Div Nutr Sci, London SE1 9NH, England
[3] Univ Manchester, Sch Mat, Manchester M1 7HS, Lancs, England
[4] Univ Manchester, Fac Med & Human Sci, Inst Cardiovasc Sci, Manchester M13 9NT, Lancs, England
[5] Univ Manchester, Fac Life Sci, Manchester M13 9PT, Lancs, England
[6] Univ Liverpool, Dept Phys, Surface Sci Res Ctr, Liverpool L69 3GH, Merseyside, England
[7] Univ Manchester, Manchester Acad & Hlth Sci Ctr, Inst Inflammat & Repair, Manchester M13 9PT, Lancs, England
基金
英国工程与自然科学研究理事会; 英国惠康基金; 英国医学研究理事会;
关键词
Arterial stiffening; Fibrillin microfibrils; Type; 1; diabetes; Extracellular matrix; Mechanical properties; FIBRILLIN-RICH MICROFIBRILS; EXTRACELLULAR-MATRIX; ELASTIC PROPERTIES; MARFAN-SYNDROME; CONNECTIVE TISSUES; MARKED LONGEVITY; VI COLLAGEN; MELLITUS; RATS; METALLOPROTEINASES;
D O I
10.1016/j.actbio.2014.07.001
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Diabetes is strongly associated with cardiovascular disease, but the mechanisms, structural and biomechanical consequences of aberrant blood vessel remodelling remain poorly defined. Using an experimental (streptozotocin, STZ) rat model of diabetes, we hypothesized that diabetes enhances extracellular protease activity in the aorta and induces morphological, compositional and localized micromechanical tissue remodelling. We found that the medial aortic layer underwent significant thickening in diabetic animals but without significant changes in collagen or elastin (abundance). Scanning acoustic microscopy demonstrated that such tissue remodelling was associated with a significant decrease in acoustic wave speed (an indicator of reduced material stiffness) in the inter-lamellar spaces of the vessel wall. This index of decreased stiffness was also linked to increased extracellular protease activity (assessed by semi-quantitative in situ gelatin zymography). Such a proteolytically active environment may affect the macromolecular structure of long-lived extracellular matrix molecules. To test this hypothesis, we also characterized the effects of diabetes on the ultrastructure of an important elastic fibre component: the fibrillin microfibril. Using size exclusion chromatography and atomic force microscopy, we isolated and imaged microfibrils from both healthy and diabetic aortas. Microfibrils derived from diabetic tissues were fragmented, morphologically disrupted and weakened (as assessed following molecular combing). These structural and functional abnormalities were not replicated by in vitro glycation. Our data suggest that proteolysis may be a key driver of localized mechanical change in the inter-lamellar space of diabetic rat aortas and that structural proteins (such as fibrillin microfbrils) may be biomarkers of diabetes induced damage. (C) 2014 Acta Materialia Inc. Published by Elsevier Ltd. This is an open access article under the CC BY license
引用
收藏
页码:4843 / 4851
页数:9
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