2
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Intensity distribution segmentation in ultrafast Doppler combined with scanning laser confocal microscopy for assessing vascular changes associated with ageing in murine hippocampi

      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 hippocampus plays an important role in learning and memory, requiring high-neuronal oxygenation. Understanding the relationship between blood flow and vascular structure—and how it changes with ageing—is physiologically and anatomically relevant. Ultrafast Doppler ( \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\mu$$\end{document} Doppler) and scanning laser confocal microscopy (SLCM) are powerful imaging modalities that can measure in vivo cerebral blood volume (CBV) and post mortem vascular structure, respectively. Here, we apply both imaging modalities to a cross-sectional and longitudinal study of hippocampi vasculature in wild-type mice brains. We introduce a segmentation of CBV distribution obtained from \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\mu$$\end{document} Doppler and show that this mice-independent and mesoscopic measurement is correlated with vessel volume fraction (VVF) distribution obtained from SLCM—e.g., high CBV relates to specific vessel locations with large VVF. Moreover, we find significant changes in CBV distribution and vasculature due to ageing (5 vs. 21 month-old mice), highlighting the sensitivity of our approach. Overall, we are able to associate CBV with vascular structure—and track its longitudinal changes—at the artery-vein, venules, arteriole, and capillary levels. We believe that this combined approach can be a powerful tool for studying other acute (e.g., brain injuries), progressive (e.g., neurodegeneration) or induced pathological changes.

          Related collections

          Most cited references49

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          Re-epithelialization and immune cell behaviour in an ex vivo human skin model

          A large body of literature is available on wound healing in humans. Nonetheless, a standardized ex vivo wound model without disruption of the dermal compartment has not been put forward with compelling justification. Here, we present a novel wound model based on application of negative pressure and its effects for epidermal regeneration and immune cell behaviour. Importantly, the basement membrane remained intact after blister roof removal and keratinocytes were absent in the wounded area. Upon six days of culture, the wound was covered with one to three-cell thick K14+Ki67+ keratinocyte layers, indicating that proliferation and migration were involved in wound closure. After eight to twelve days, a multi-layered epidermis was formed expressing epidermal differentiation markers (K10, filaggrin, DSG-1, CDSN). Investigations about immune cell-specific manners revealed more T cells in the blister roof epidermis compared to normal epidermis. We identified several cell populations in blister roof epidermis and suction blister fluid that are absent in normal epidermis which correlated with their decrease in the dermis, indicating a dermal efflux upon negative pressure. Together, our model recapitulates the main features of epithelial wound regeneration, and can be applied for testing wound healing therapies and investigating underlying mechanisms.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Adult hippocampal neurogenesis is abundant in neurologically healthy subjects and drops sharply in patients with Alzheimer’s disease

            The hippocampus is one of the most affected areas in Alzheimer's disease (AD)1. Moreover, this structure hosts one of the most unique phenomena of the adult mammalian brain, namely, the addition of new neurons throughout life2. This process, called adult hippocampal neurogenesis (AHN), confers an unparalleled degree of plasticity to the entire hippocampal circuitry3,4. Nonetheless, direct evidence of AHN in humans has remained elusive. Thus, determining whether new neurons are continuously incorporated into the human dentate gyrus (DG) during physiological and pathological aging is a crucial question with outstanding therapeutic potential. By combining human brain samples obtained under tightly controlled conditions and state-of-the-art tissue processing methods, we identified thousands of immature neurons in the DG of neurologically healthy human subjects up to the ninth decade of life. These neurons exhibited variable degrees of maturation along differentiation stages of AHN. In sharp contrast, the number and maturation of these neurons progressively declined as AD advanced. These results demonstrate the persistence of AHN during both physiological and pathological aging in humans and provide evidence for impaired neurogenesis as a potentially relevant mechanism underlying memory deficits in AD that might be amenable to novel therapeutic strategies.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Neurogenesis in the adult human hippocampus.

              The genesis of new cells, including neurons, in the adult human brain has not yet been demonstrated. This study was undertaken to investigate whether neurogenesis occurs in the adult human brain, in regions previously identified as neurogenic in adult rodents and monkeys. Human brain tissue was obtained postmortem from patients who had been treated with the thymidine analog, bromodeoxyuridine (BrdU), that labels DNA during the S phase. Using immunofluorescent labeling for BrdU and for one of the neuronal markers, NeuN, calbindin or neuron specific enolase (NSE), we demonstrate that new neurons, as defined by these markers, are generated from dividing progenitor cells in the dentate gyrus of adult humans. Our results further indicate that the human hippocampus retains its ability to generate neurons throughout life.
                Bookmark

                Author and article information

                Contributors
                akun@fcien.edu.uy
                jbrum@fisica.edu.uy
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                26 April 2022
                26 April 2022
                2022
                : 12
                : 6784
                Affiliations
                [1 ]GRID grid.11630.35, ISNI 0000000121657640, Laboratorio de Acústica Ultrasonora, Instituto de Física, Facultad de Ciencias, , Universidad de la República, ; 11400 Montevideo, Uruguay
                [2 ]GRID grid.11630.35, ISNI 0000000121657640, Física No Lineal, Instituto de Física de Facultad de Ciencias, , Universidad de la República, ; 11400 Montevideo, Uruguay
                [3 ]GRID grid.482688.8, ISNI 0000 0001 2323 2857, Laboratorio de Biología Celular del Sistema Nervioso Periférico, Departamento de Proteínas y Ácidos Nucleicos, , Instituto de Investigaciones Biológicas Clemente Estable, ; 11600 Montevideo, Uruguay
                [4 ]GRID grid.413448.e, ISNI 0000 0000 9314 1427, Chronic Disease Programme (UFIEC), Instituto de Salud Carlos III, , CIBERNED and CIEN Foundation, ; 28220 Madrid, Spain
                [5 ]GRID grid.15736.36, ISNI 0000 0001 1882 0021, Physics for Medicine Paris, , Inserm U1273, ESPCI Paris, PSL University, CNRS UMR 8063, ; 75012 Paris, France
                [6 ]GRID grid.11630.35, ISNI 0000000121657640, Departamento de Biociencias Veterinarias, Facultad de Veterinaria, , Universidad de la República, ; 13000 Montevideo, Uruguay
                [7 ]GRID grid.7107.1, ISNI 0000 0004 1936 7291, Present Address: Institute for Complex Systems and Mathematical Biology, , University of Aberdeen, King’s College, ; Aberdeen, AB24 3UE UK
                Article
                10457
                10.1038/s41598-022-10457-9
                9042937
                35473942
                d61e46e9-469d-4366-8a23-729427b03155
                © The Author(s) 2022

                Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 23 November 2021
                : 6 April 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100008725, Agencia Nacional de Investigación e Innovación;
                Award ID: FCE_1_2019_1_155539
                Funded by: Sistema Nacional de Investigadores (SNI), ANII, Uruguay
                Funded by: Programa de Desarrollo de las Ciencias Básicas (PEDECIBA)
                Funded by: FundRef http://dx.doi.org/10.13039/501100006049, Comisión Sectorial de Investigación Científica;
                Award ID: CSIC2018-FID 13-Grupo ID 722
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s) 2022

                Uncategorized
                confocal microscopy,ultrasound,neural ageing,imaging techniques,ageing
                Uncategorized
                confocal microscopy, ultrasound, neural ageing, imaging techniques, ageing

                Comments

                Comment on this article