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      PDGF-B Is Required for Development of the Glymphatic System

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          SUMMARY

          The glymphatic system is a highly polarized cerebrospinal fluid (CSF) transport system that facilitates the clearance of neurotoxic molecules through a brain-wide network of perivascular pathways. Herein we have mapped the development of the glymphatic system in mice. Perivascular CSF transport first emerges in hippocampus in newborn mice, and a mature glymphatic system is established in the cortex at 2 weeks of age. Formation of astrocytic endfeet and polarized expression of aquaporin 4 (AQP4) consistently coincided with the appearance of perivascular CSF transport. Deficiency of platelet-derived growth factor B (PDGF-B) function in the PDGF retention motif knockout mouse line Pdgfb ret/ret suppressed the development of the glymphatic system, whose functions remained suppressed in adulthood compared with wild-type mice. These experiments map the natural development of the glymphatic system in mice and define a critical role of PDGF-B in the development of perivascular CSF transport.

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          In Brief

          Munk et al. unravel the developmental profile of the glia-lymphatic (glymphatic) system. Glymphatic function arises in the hippocampus at postnatal day 1 in conjunction with the polarized expression of AQP4 at astrocyte endfeet. PDGF-B signaling is implicated in normal glymphatic function, and reduced signaling reduces AQP4 polarization and glymphatic influx.

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          Most cited references45

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          Pericyte loss and microaneurysm formation in PDGF-B-deficient mice.

          Platelet-derived growth factor (PDGF)-B-deficient mouse embryos were found to lack microvascular pericytes, which normally form part of the capillary wall, and they developed numerous capillary microaneurysms that ruptured at late gestation. Endothelial cells of the sprouting capillaries in the mutant mice appeared to be unable to attract PDGF-Rbeta-positive pericyte progenitor cells. Pericytes may contribute to the mechanical stability of the capillary wall. Comparisons made between PDGF null mouse phenotypes suggest a general role for PDGFs in the development of myofibroblasts.
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            Local generation of glia is a major astrocyte source in postnatal cortex.

            Glial cells constitute nearly 50% of the cells in the human brain. Astrocytes, which make up the largest glial population, are crucial to the regulation of synaptic connectivity during postnatal development. Because defects in astrocyte generation are associated with severe neurological disorders such as brain tumours, it is important to understand how astrocytes are produced. Astrocytes reportedly arise from two sources: radial glia in the ventricular zone and progenitors in the subventricular zone, with the contribution from each region shifting with time. During the first three weeks of postnatal development, the glial cell population, which contains predominantly astrocytes, expands 6-8-fold in the rodent brain. Little is known about the mechanisms underlying this expansion. Here we show that a major source of glia in the postnatal cortex in mice is the local proliferation of differentiated astrocytes. Unlike glial progenitors in the subventricular zone, differentiated astrocytes undergo symmetric division, and their progeny integrate functionally into the existing glial network as mature astrocytes that form endfeet with blood vessels, couple electrically to neighbouring astrocytes, and take up glutamate after neuronal activity.
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              Electrical resistance across the blood-brain barrier in anaesthetized rats: a developmental study.

              1. Ion permeability of the blood-brain barrier was studied by in situ measurement of transendothelial electrical resistance in anaesthetized rats aged between 17 days gestation and 33 days after birth, and by electron microscopic examination of lanthanum permeability in fetal and neonatal rats aged up to 10 days old. 2. The blood-brain barrier in 17- to 20-day fetuses had a resistance of 310 omega cm2 but was impermeable to lanthanum, and therefore had properties intermediate between leaky and tight epithelia. 3. From 21 days gestation, the resistance was 1128 omega cm2, indicating a tight blood-brain barrier and low ion permeability. There was little further change in barrier resistance after birth, and in 28- to 33-day rats, when the brain barrier systems are mature in other ways, vessels had a mean resistance of 1462 omega cm2. 4. In the tight blood-brain barrier, arterial vessels had a significantly higher resistance than venous vessels, 1490 and 918 omega cm2 respectively. In vessels less than 50 microns diameter and within the normal 60 min experimental period, there was no significant variation in vessel resistance. 5. Hyperosmotic shock caused a rapid decay in resistance (maximal within 5 min), and after disruption of the blood-brain barrier, vessel resistance was 100-300 omega cm2 in both arterial and venous vessels, and the effect was reversible. After the application of metabolic poisons (NaCN plus iodoacetate) and low temperature there was a similarly low electrical resistance. 6. It is concluded that the increase in electrical resistance at birth indicates a decrease in paracellular ion permeability at the blood-brain barrier and is required for effective brain interstitial fluid ion regulation.
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                Author and article information

                Journal
                101573691
                39703
                Cell Rep
                Cell Rep
                Cell reports
                2211-1247
                25 March 2019
                12 March 2019
                03 April 2019
                : 26
                : 11
                : 2955-2969.e3
                Affiliations
                [1 ]Center for Translational Neuromedicine, University of Rochester, Rochester, NY 14642, USA
                [2 ]Center for Basic and Translational Neuroscience, University of Copenhagen, 2200 Copenhagen, Denmark
                [3 ]Department of Experimental Medical Science, Lund University, 221 84 Lund, Sweden
                [4 ]Wallenberg Center for Molecular Medicine, Lund University, 221 84 Lund, Sweden
                [5 ]Mansoura University Hospital, Faculty of Medicine, Mansoura University, 35516 Mansoura, Egypt
                [6 ]Department of Immunology, Genetics and Pathology, Uppsala University, 751 85 Uppsala, Sweden
                [7 ]Department of Mechanical Engineering, University of Rochester, Rochester, NY 14627, USA
                [8 ]Integrated Cardio Metabolic Center (ICMC), Karolinska Institutet, Novum, 141 57 Huddinge, Sweden
                [9 ]Department of Cellular and Molecular Medicine, University of Copenhagen, 2200 Copenhagen, Denmark
                [10 ]These authors contributed equally
                [11 ]These authors contributed equally
                [12 ]Lead Contact
                Author notes

                AUTHOR CONTRIBUTIONS

                A.S.M., W.W., N.B.B., A.M.E., A.X.C., B.S., A.B., M.A.M., B.T.K., D.H.K., K.M., A.M., and I.L. performed experiments and analyzed data. A.S.M., C.B., K.M., M.N., and I.L. wrote the manuscript. C.B., K.M., A.M., M.N., and I.L. contributed reagents.

                Article
                NIHMS1523852
                10.1016/j.celrep.2019.02.050
                6447074
                30865886
                8f34e502-7afe-47a3-8c68-b83b16828e9d

                This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/).

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                Cell biology
                Cell biology

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