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      A simple, one-step polychromatic staining method for epoxy-embedded semithin tissue sections

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          Abstract

          A simple polychromatic staining method for epoxy-embedded semi-thin tissue sections was developed to allow more informative and convincing histological investigation in various fields of research and education. This technique enabled clear differentiation of various tissue structures according to color tone and intensity, thereby facilitating the detection of fine structural differences.

          Abstract

          Although conventional toluidine blue staining is a common technique used for rapid observation of semithin sections prior to transmission electron microscopy, it is monochromatic and insufficient for accurate identification of different tissue components by light microscopy. Additionally, polychromatic staining methods generally require step-by-step processes involving different dyes, and it is often difficult to balance the color tone of each step. In this study, we developed a simple polychromatic staining method for epoxy-embedded tissue sections. We stained preheated sections with an aqueous ethanol solution of azure B and basic fuchsin, with the addition of sodium tetraborate to enhance the staining efficacy. We optimized various staining conditions to enable sufficient coloration easily and consistently in a single, rapid staining step, using a single staining-mixture solution. Our method enabled clear differentiation of various tissue structures according to color tone and stain intensity, thereby facilitating the detection of fine structural differences, including various organelle and inclusion bodies. This technique represents a simple polychrome-staining method to allow more informative and convincing histological investigation in various fields of research and education.

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          Most cited references26

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          Embedding in epoxy resins for ultrathin sectioning in electron microscopy.

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            Functional biology of intestinal goblet cells.

            Goblet cells reside throughout the length of the small and large intestine and are responsible for the production and maintenance of the protective mucus blanket by synthesizing and secreting high-molecular-weight glycoproteins known as mucins. To elucidate the role of goblet cells in the biology of the intestinal tract, an overview of the physiological implications of the mucus gel is presented, including a concise review of the products secreted by the cell. Because of the unique nature of this highly polarized exocrine cell, the maturational reorganization of the cytoarchitecture and the cellular mechanisms by which goblet cells secrete their products are discussed. This includes elucidation of the baseline secretory pathway, which is dependent on the cytoskeleton for granule movement, and the accelerated secretory pathway, which is independent of the cytoskeleton but requires an extracellular signal to occur. Finally, the involvement of goblet cell mucins in the pathophysiology of intestinal neoplasia and ulcerative colitis are presented.
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              Morphological and functional characterization of non-alcoholic fatty liver disease induced by a methionine-choline-deficient diet in C57BL/6 mice.

              Non-alcoholic fatty liver disease (NAFLD), including non-alcoholic steatohepatitis (NASH), appears to be increasingly common worldwide. Its histopathology and the effects of nutrition on liver function have not been fully determined. To elucidate the cellular mechanisms of NAFLD induced by a methionine-choline-deficient (MCD) diet in mice. Particular focus was placed on the role of phagocytic cells. Male C57BL/6 mice were fed an MCD diet for 30 weeks. A recovery model was also established wherein a normal control diet was provided for 2 weeks after a period of 8, 16, or 30 weeks. Mice fed the MCD diet for ≥ 2 weeks exhibited severe steatohepatitis with elevated serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels. Steatohepatitis was accompanied by the infiltration of CD68-positive macrophages (Kupffer cells). The severity of steatohepatitis increased in the first 16 weeks but was seen to lessen by week 30. Fibrosis began to develop at 10 weeks and continued thereafter. Steatohepatitis and elevated serum hepatic enzyme concentrations returned to normal levels after switching the diet back to the control within the first 16 weeks, but fibrosis and CD68-positive macrophages remained. The histopathological changes and irreversible fibrosis seen in this model were caused by prolonged feeding of an MCD diet. These results were accompanied by changes in the activity of CD68-positive cells with temporary elevation of CCL-2, MMP-13, and MMP-9 levels, all of which may trigger early steatohepatitis and late fibrosis through phagocytosis-associated MMP induction.
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                Author and article information

                Journal
                Microscopy (Oxf)
                Microscopy (Oxf)
                jmicro
                Microscopy
                Oxford University Press
                2050-5698
                2050-5701
                December 2018
                15 October 2018
                15 October 2018
                : 67
                : 6
                : 331-344
                Affiliations
                [1 ]Department of Anatomy and Developmental Biology, Tokyo Women’s Medical University, 8-1 Kawada-Cho, Shinjuku, Tokyo, Japan
                [2 ]Department of Chemistry, Tokyo Women’s Medical University, 8-1 Kawada-Cho, Shinjuku, Tokyo, Japan
                Author notes
                To whom correspondence should be addressed. Tel: (+81) 3-5269-7406, Fax: (+81) 3-5269-7407, E-mail: ezakit@ 123456twmu.ac.jp

                This is the posthumous work of Shunichi Morikawa, who unfortunately passed away on 28 July 2017, during the preparation of this manuscript.

                Article
                dfy037
                10.1093/jmicro/dfy037
                6278751
                30321369
                83c1cbef-2603-4378-9276-193247d06725
                © The Author(s) 2018. Published by Oxford University Press on behalf of The Japanese Society of Microscopy.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 12 June 2018
                : 06 August 2018
                : 30 August 2018
                Page count
                Pages: 14
                Funding
                Funded by: Japan Society for the Promotion of Science 10.13039/501100001691
                Award ID: 23590245
                Categories
                Article

                polychromatic staining,epoxy resin,semithin section,azure b,basic fuchsin,tetraborate,light microscopy

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