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      Deciphering microvascular changes after myocardial infarction through 3D fully automated image analysis

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          Abstract

          The microvasculature continuously adapts in response to pathophysiological conditions to meet tissue demands. Quantitative assessment of the dynamic changes in the coronary microvasculature is therefore crucial in enhancing our knowledge regarding the impact of cardiovascular diseases in tissue perfusion and in developing efficient angiotherapies. Using confocal microscopy and thick tissue sections, we developed a 3D fully automated pipeline that allows to precisely reconstruct the microvasculature and to extract parameters that quantify all its major features, its relation to smooth muscle actin positive cells and capillary diffusion regions. The novel pipeline was applied in the analysis of the coronary microvasculature from healthy tissue and tissue at various stages after myocardial infarction (MI) in the pig model, whose coronary vasculature closely resembles that of human tissue. We unravelled alterations in the microvasculature, particularly structural changes and angioadaptation in the aftermath of MI. In addition, we evaluated the extracted knowledge’s potential for the prediction of pathophysiological conditions in tissue, using different classification schemes. The high accuracy achieved in this respect, demonstrates the ability of our approach not only to quantify and identify pathology-related changes of microvascular beds, but also to predict complex and dynamic microvascular patterns.

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          Angiogenesis in life, disease and medicine.

          The growth of blood vessels (a process known as angiogenesis) is essential for organ growth and repair. An imbalance in this process contributes to numerous malignant, inflammatory, ischaemic, infectious and immune disorders. Recently, the first anti-angiogenic agents have been approved for the treatment of cancer and blindness. Angiogenesis research will probably change the face of medicine in the next decades, with more than 500 million people worldwide predicted to benefit from pro- or anti-angiogenesis treatments.
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            Topographic distance and watershed lines

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              Microcirculation and Hemorheology.

              Major experimental and theoretical studies on microcirculation and hemorheology are reviewed with the focus on mechanics of blood flow and the vascular wall. Flow of the blood formed elements (red blood cells (RBCs), white blood cells or leukocytes (WBCs) and platelets) in individual arterioles, capillaries and venules, and in microvascular networks is discussed. Mechanical and rheological properties of the formed elements and their interactions with the vascular wall are reviewed. Short-term and long-term regulation of the microvasculature is discussed; the modes of regulation include metabolic, myogenic and shear-stress-dependent mechanisms as well as vascular adaptation such as angiogenesis and vascular remodeling.
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                Author and article information

                Contributors
                agarroyo@cnic.es
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                30 January 2018
                30 January 2018
                2018
                : 8
                : 1854
                Affiliations
                [1 ]ISNI 0000 0001 0125 7682, GRID grid.467824.b, Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), ; Madrid, 28029 Spain
                [2 ]ISNI 0000 0001 2171 9311, GRID grid.21107.35, Department of Biomedical Engineering, School of Medicine, , Johns Hopkins University, ; Baltimore, MD 21205 USA
                [3 ]ISNI 0000 0000 9314 1427, GRID grid.413448.e, Centro de Investigación Biomédica en Red de Enfermedades CardioVasculares (CIBERCV), ; Madrid, Spain
                [4 ]GRID grid.419651.e, IIS-Fundación Jiménez Díaz, ; Madrid, Spain
                [5 ]ISNI 0000 0001 2151 2978, GRID grid.5690.a, Biomedical Image Technologies (BIT), ETSI Telecomunicación, Universidad Politécnica de Madrid, ; Madrid, 28040 Spain
                [6 ]ISNI 0000 0000 9314 1427, GRID grid.413448.e, Centro de Investigación Biomédica en Red de Bioingeniería, Biomateriales y Nanomedicina (CIBERBBN), ; Madrid, Spain
                [7 ]ISNI 0000 0001 2375 3628, GRID grid.252838.6, Present Address: Division of Science, Mathematics, and Computing, Bard College, Annandale-on-Hudson, ; NY, 12504 USA
                Author information
                http://orcid.org/0000-0003-1002-9467
                Article
                19758
                10.1038/s41598-018-19758-4
                5789835
                29382844
                58312165-6909-4b41-b418-fd818e40f776
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 29 August 2017
                : 8 January 2018
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