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      Zika virus impairs the development of blood vessels in a mouse model of congenital infection

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          Abstract

          Zika virus (ZIKV) is associated with brain development abnormalities such as primary microcephaly, a severe reduction in brain growth. Here we demonstrated in vivo the impact of congenital ZIKV infection in blood vessel development, a crucial step in organogenesis. ZIKV was injected intravenously in the pregnant type 2 interferon (IFN)-deficient mouse at embryonic day (E) 12.5. The embryos were collected at E15.5 and postnatal day (P)2. Immunohistochemistry for cortical progenitors and neuronal markers at E15.5 showed the reduction of both populations as a result of ZIKV infection. Using confocal 3D imaging, we found that ZIKV infected brain sections displayed a reduction in the vasculature density and vessel branching compared to mocks at E15.5; altogether, cortical vessels presented a comparatively immature pattern in the infected tissue. These impaired vascular patterns were also apparent in the placenta and retina. Moreover, proteomic analysis has shown that angiogenesis proteins are deregulated in the infected brains compared to controls. At P2, the cortical size and brain weight were reduced in comparison to mock-infected animals. In sum, our results indicate that ZIKV impairs angiogenesis in addition to neurogenesis during development. The vasculature defects represent a limitation for general brain growth but also could regulate neurogenesis directly.

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          VEGF as a Key Mediator of Angiogenesis in Cancer

          Vascular endothelial growth factor (VEGF) is a homodimeric glycoprotein with a molecular weight of approximately 45 kDa. It is the key mediator of angiogenesis (the formation of new blood vessels), and binds two VEGF receptors (VEGF receptor-1 and VEGF receptor-2), which are expressed on vascular endothelial cells. In healthy humans, VEGF promotes angiogenesis in embryonic development and is important in wound healing in adults. VEGF is the key mediator of angiogenesis in cancer, in which it is up-regulated by oncogene expression, a variety of growth factors and also hypoxia. Angiogenesis is essential for cancer development and growth: before a tumor can grow beyond 1–2 mm, it requires blood vessels for nutrients and oxygen. The production of VEGF and other growth factors by the tumor results in the ‘angiogenic switch’, where new vasculature is formed in and around the tumor, allowing it to grow exponentially. Tumor vasculature formed under the influence of VEGF is structurally and functionally abnormal. Blood vessels are irregularly shaped, tortuous, have dead ends and are not organized into venules, arterioles and capillaries. They are also leaky and hemorrhagic, which leads to high interstitial pressure. These characteristics mean that tumor blood flow is suboptimal, resulting in hypoxia and further VEGF production. This central role of VEGF in the production of tumor vasculature makes it a rational target for anticancer therapy.
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            Neurons derived from radial glial cells establish radial units in neocortex.

            The neocortex of the adult brain consists of neurons and glia that are generated by precursor cells of the embryonic ventricular zone. In general, glia are generated after neurons during development, but radial glia are an exception to this rule. Radial glia are generated before neurogenesis and guide neuronal migration. Radial glia are mitotically active throughout neurogenesis, and disappear or become astrocytes when neuronal migration is complete. Although the lineage relationships of cortical neurons and glia have been explored, the clonal relationship of radial glia to other cortical cells remains unknown. It has been suggested that radial glia may be neuronal precursors, but this has not been demonstrated in vivo. We have used a retroviral vector encoding enhanced green fluorescent protein to label precursor cells in vivo and have examined clones 1-3 days later using morphological, immunohistochemical and electrophysiological techniques. Here we show that clones consist of mitotic radial glia and postmitotic neurons, and that neurons migrate along clonally related radial glia. Time-lapse images show that proliferative radial glia generate neurons. Our results support the concept that a lineage relationship between neurons and proliferative radial glia may underlie the radial organization of neocortex.
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              Vascular niche for adult hippocampal neurogenesis.

              The thin lamina between the hippocampal hilus and granule cell layer, or subgranule zone (SGZ), is an area of active proliferation within the adult hippocampus known to generate new neurons throughout adult life. Although the neuronal fate of many dividing cells is well documented, little information is available about the phenotypes of cells in S-phase or how the dividing cells might interact with neighboring cells in the process of neurogenesis. Here, we make the unexpected observation that dividing cells are found in dense clusters associated with the vasculature and roughly 37% of all dividing cells are immunoreactive for endothelial markers. Most of the newborn endothelial cells disappear over several weeks, suggesting that neurogenesis is intimately associated with a process of active vascular recruitment and subsequent remodeling. The present data provide the first evidence that adult neurogenesis occurs within an angiogenic niche. This environment may provide a novel interface where mesenchyme-derived cells and circulating factors influence plasticity in the adult central nervous system. Copyright 2000 Wiley-Liss, Inc.
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                Author and article information

                Contributors
                ppgarcez@gmail.com
                hstolp@rvc.ac.uk
                zoltan.molnar@dpag.ox.ac.uk
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                24 August 2018
                24 August 2018
                2018
                : 8
                : 12774
                Affiliations
                [1 ]ISNI 0000 0001 2294 473X, GRID grid.8536.8, Institute of Biomedical Sciences, , Federal University of Rio de Janeiro, ; Rio de Janeiro, Brazil
                [2 ]ISNI 0000 0004 1936 8948, GRID grid.4991.5, Department of Physiology, Anatomy and Genetics, , University of Oxford, ; Oxford, UK
                [3 ]ISNI 0000 0001 2322 6764, GRID grid.13097.3c, Centre for the Developing Brain, Department of Perinatal Imaging & Health, King’s College London, ; London, UK
                [4 ]ISNI 0000 0001 2294 473X, GRID grid.8536.8, Microbiology Institute Paulo de Góes, Federal University of Rio de Janeiro, ; Rio de Janeiro, Brazil
                [5 ]ISNI 0000 0001 2294 473X, GRID grid.8536.8, Institute of Biology, , Federal University of Rio de Janeiro, ; Rio de Janeiro, Brazil
                [6 ]ISNI 0000 0001 2294 473X, GRID grid.8536.8, Institute of Biophysics Carlos Chagas Filho, , Federal University of Rio de Janeiro, ; Rio de Janeiro, Brazil
                [7 ]ISNI 0000 0001 2294 473X, GRID grid.8536.8, Nuclear Instrumentation Laboratory, , Federal University of Rio de Janeiro, ; Rio de Janeiro, Brazil
                [8 ]GRID grid.472984.4, D’Or Institute for Research and Education (IDOR), ; Rio de Janeiro, Brazil
                [9 ]ISNI 0000 0001 2184 6919, GRID grid.411173.1, Department of Neurobiology, Institute of Biology, , Fluminense Federal University, ; Niterói, Brazil
                Author information
                http://orcid.org/0000-0002-9107-1335
                http://orcid.org/0000-0003-1953-7871
                http://orcid.org/0000-0002-0225-1132
                http://orcid.org/0000-0002-6852-6004
                Article
                31149
                10.1038/s41598-018-31149-3
                6109170
                30143723
                0793df50-605e-44a2-b63f-d5f4651aeaf9
                © 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
                : 12 April 2018
                : 13 August 2018
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