6
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      The arrangements of the microvasculature and surrounding glial cells are linked to blood–brain barrier formation in the cerebral cortex

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The blood–brain barrier (BBB) blocks harmful substances from entering the brain and dictates the central nervous system (CNS)-specific pharmacokinetics. Recent studies have shown that perivascular astrocytes and microglia also control BBB functions, however, information about the formation of BBB glial architecture remains scarce. We investigated the time course of the formation of BBB glial architecture in the rat brain cerebral cortex using Evans blue (EB) and tissue fixable biotin (Sulfo-NHS Biotin). The extent of the leakage into the brain parenchyma showed that the BBB was not formed at postnatal Day 4 (P4). The BBB gradually strengthened and reached a plateau at P15. We then investigated the changes in the configurations of blood vessels, astrocytes, and microglia with age by 3D image reconstruction of the immunohistochemical data. The endfeet of astrocytes covered the blood vessels, and the coverage rate rapidly increased after birth and reached a plateau at P15. Interestingly, microglia were also in contact with the capillaries, and the coverage rate was highest at P15 and stabilized at P30. It was also clarified that the microglial morphology changed from the amoeboid type to the ramified type, while the areas of the respective contact sites became smaller during P4 and P15. These results suggest that the perivascular glial architecture formation of the rat BBB occurs from P4 to P15 because the paracellular transport and the arrangements of perivascular glial cells at P15 are totally the same as those of P30. In addition, the contact style of perivascular microglia dramatically changed during P4-P15.

          Related collections

          Most cited references64

          • Record: found
          • Abstract: found
          • Article: not found

          Fate mapping analysis reveals that adult microglia derive from primitive macrophages.

          Microglia are the resident macrophages of the central nervous system and are associated with the pathogenesis of many neurodegenerative and brain inflammatory diseases; however, the origin of adult microglia remains controversial. We show that postnatal hematopoietic progenitors do not significantly contribute to microglia homeostasis in the adult brain. In contrast to many macrophage populations, we show that microglia develop in mice that lack colony stimulating factor-1 (CSF-1) but are absent in CSF-1 receptor-deficient mice. In vivo lineage tracing studies established that adult microglia derive from primitive myeloid progenitors that arise before embryonic day 8. These results identify microglia as an ontogenically distinct population in the mononuclear phagocyte system and have implications for the use of embryonically derived microglial progenitors for the treatment of various brain disorders.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo.

            Microglial cells represent the immune system of the mammalian brain and therefore are critically involved in various injuries and diseases. Little is known about their role in the healthy brain and their immediate reaction to brain damage. By using in vivo two-photon imaging in neocortex, we found that microglial cells are highly active in their presumed resting state, continually surveying their microenvironment with extremely motile processes and protrusions. Furthermore, blood-brain barrier disruption provoked immediate and focal activation of microglia, switching their behavior from patroling to shielding of the injured site. Microglia thus are busy and vigilant housekeepers in the adult brain.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Structure and function of the blood-brain barrier.

              Neural signalling within the central nervous system (CNS) requires a highly controlled microenvironment. Cells at three key interfaces form barriers between the blood and the CNS: the blood-brain barrier (BBB), blood-CSF barrier and the arachnoid barrier. The BBB at the level of brain microvessel endothelium is the major site of blood-CNS exchange. The structure and function of the BBB is summarised, the physical barrier formed by the endothelial tight junctions, and the transport barrier resulting from membrane transporters and vesicular mechanisms. The roles of associated cells are outlined, especially the endfeet of astrocytic glial cells, and pericytes and microglia. The embryonic development of the BBB, and changes in pathology are described. The BBB is subject to short and long-term regulation, which may be disturbed in pathology. Any programme for drug discovery or delivery, to target or avoid the CNS, needs to consider the special features of the BBB.
                Bookmark

                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/387577/overviewRole: Role: Role: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/2751463/overviewRole: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/370790/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role: Role: Role: Role: Role:
                Journal
                Front Neuroanat
                Front Neuroanat
                Front. Neuroanat.
                Frontiers in Neuroanatomy
                Frontiers Media S.A.
                1662-5129
                07 August 2024
                2024
                : 18
                : 1438190
                Affiliations
                Division of Pharmacology, Laboratory of Neuropharmacology, National Institute of Health Sciences , Kawasaki, Japan
                Author notes

                Edited by: Jon Storm-Mathisen, University of Oslo, Norway

                Reviewed by: Gabriela Hurtado-Alvarado, Universidad Nacional Autónoma de México, Mexico

                Tamar Licht, Hebrew University of Jerusalem, Israel

                *Correspondence: Kaoru Sato, kasato@ 123456nihs.go.jp
                Article
                10.3389/fnana.2024.1438190
                11335649
                39170850
                2acfc5e5-2009-4efe-993a-143e974f0523
                Copyright © 2024 Shigemoto-Mogami, Nakayama-Kitamura and Sato.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 25 May 2024
                : 29 July 2024
                Page count
                Figures: 6, Tables: 0, Equations: 0, References: 64, Pages: 13, Words: 8789
                Funding
                Funded by: Japan Agency for Medical Research and Development, doi 10.13039/100009619;
                The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This work was supported by Japan Agency for Medical Research and Development. This research was supported in part by research grants from AMED (23be1004101j0002, 23mk0101222j0102, 23ak0101187j0102).
                Categories
                Neuroscience
                Original Research

                Neurosciences
                microglia,astrocytes,bbb,development,three-dimensional distribution,glia limitans
                Neurosciences
                microglia, astrocytes, bbb, development, three-dimensional distribution, glia limitans

                Comments

                Comment on this article