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      Development of a Novel Ex-vivo 3D Model to Screen Amoebicidal Activity on Infected Tissue

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          Abstract

          Amoebiasis is a parasitic disease that causes thousands of deaths every year, its adverse effects and resistance to conventional treatments have led to the search of new treatment options, as well as the development of novel screening methods. In this work, we implemented a 3D model of intestine and liver slices from hamsters that were infected ex vivo with virulent E. histolytica trophozoites. Results show preserved histology in both uninfected tissues as well as ulcerations, destruction of the epithelial cells, and inflammatory reaction in intestine slices and formation of micro abscesses, and the presence of amoebae in the sinusoidal spaces and in the interior of central veins in liver slices. The three chemically synthetized compounds T-001, T-011, and T-016, which act as amoebicides in vitro, were active in both infected tissues, as they decreased the number of trophozoites, and provoked death by disintegration of the amoeba, similar to metronidazole. However, compound T-011 induced signs of cytotoxicity to liver slices. Our results suggest that ex vivo cultures of precision-cut intestinal and liver slices represent a reliable 3D approach to evaluate novel amoebicidal compounds, and to simultaneously detect their toxicity, while reducing the number of experimental animals commonly required by other model systems.

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          Preparation and incubation of precision-cut liver and intestinal slices for application in drug metabolism and toxicity studies.

          Precision-cut tissue slices (PCTS) are viable ex vivo explants of tissue with a reproducible, well defined thickness. They represent a mini-model of the organ under study and contain all cells of the tissue in their natural environment, leaving intercellular and cell-matrix interactions intact, and are therefore highly appropriate for studying multicellular processes. PCTS are mainly used to study the metabolism and toxicity of xenobiotics, but they are suitable for many other purposes. Here we describe the protocols to prepare and incubate rat and human liver and intestinal slices. Slices are prepared from fresh liver by making a cylindrical core using a drill with a hollow bit, from which slices are cut with a specially designed tissue slicer. Intestinal tissue is embedded in cylinders of agarose before slicing. Slices remain viable for 24 h (intestine) and up to 96 h (liver) when incubated in 6- or 12-well plates under 95% O(2)/5% CO(2) atmosphere.
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            Vero cell platform in vaccine production: moving towards cell culture-based viral vaccines.

            The development of cell culture systems for virus propagation has led to major advances in virus vaccine development. Primary and diploid cell culture systems are now being replaced by the use of continuous cell lines (CCLs). These substrates are gaining increasing acceptance from regulatory authorities as improved screening technologies remove fears regarding their potential oncogenic properties. The Vero cell line is the most widely accepted CCL by regulatory authorities and has been used for over 30 years for the production of polio and rabies virus vaccines. The recent licensure of a Vero cell-derived live virus vaccine (ACAM2000, smallpox vaccine) has coincided with an explosion in the development of a range of new viral vaccines, ranging from live-attenuated pediatric vaccines against rotavirus infections to inactivated whole-virus vaccines against H5N1 pandemic influenza. These developments have illustrated the value of this cell culture platform in the rapid development of vaccines against a range of virus diseases.
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              What exactly is ‘ N ’ in cell culture and animal experiments?

              Biologists determine experimental effects by perturbing biological entities or units. When done appropriately, independent replication of the entity–intervention pair contributes to the sample size (N) and forms the basis of statistical inference. If the wrong entity–intervention pair is chosen, an experiment cannot address the question of interest. We surveyed a random sample of published animal experiments from 2011 to 2016 where interventions were applied to parents and effects examined in the offspring, as regulatory authorities provide clear guidelines on replication with such designs. We found that only 22% of studies (95% CI = 17%–29%) replicated the correct entity–intervention pair and thus made valid statistical inferences. Nearly half of the studies (46%, 95% CI = 38%–53%) had pseudoreplication while 32% (95% CI = 26%–39%) provided insufficient information to make a judgement. Pseudoreplication artificially inflates the sample size, and thus the evidence for a scientific claim, resulting in false positives. We argue that distinguishing between biological units, experimental units, and observational units clarifies where replication should occur, describe the criteria for genuine replication, and provide concrete examples of in vitro, ex vivo, and in vivo experimental designs.
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                Author and article information

                Contributors
                carranza60@yahoo.com.mx
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                10 June 2019
                10 June 2019
                2019
                : 9
                : 8396
                Affiliations
                [1 ]ISNI 0000 0001 1091 9430, GRID grid.419157.f, División de Investigación en Salud, , UMAE, Hospital de Cardiología #34, Instituto Mexicano del Seguro Social, ; Monterrey, Nuevo León Mexico
                [2 ]ISNI 0000 0001 1091 9430, GRID grid.419157.f, Centro de Investigación Biomédica del Noreste, , Instituto Mexicano del Seguro Social, ; Monterrey, Nuevo León Mexico
                [3 ]ISNI 0000 0001 2203 0321, GRID grid.411455.0, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León, ; San Nicolás de los Garza, Nuevo León Mexico
                [4 ]ISNI 0000 0001 2165 8782, GRID grid.418275.d, Laboratorio de Biotecnología Farmacéutica, Centro de Biotecnología Genómica, , Instituto Politécnico Nacional, ; Reynosa, 88710 Tamaulipas Mexico
                [5 ]GRID grid.441492.e, Centro de Investigación Biomédica, Facultad de Medicina, , Universidad Autónoma de Coahuila, ; Torreón, Coahuila Mexico
                [6 ]ISNI 0000 0004 0407 1981, GRID grid.4830.f, Groningen Research Institute of Pharmacy, , University of Groningen, ; Groningen, The Netherlands
                Author information
                http://orcid.org/0000-0002-8944-9298
                Article
                44899
                10.1038/s41598-019-44899-5
                6557822
                31182753
                1c422494-8cc7-4a74-9a24-0522af9bda0e
                © The Author(s) 2019

                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
                : 16 November 2018
                : 28 May 2019
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                © The Author(s) 2019

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                cell biology,gastrointestinal models
                Uncategorized
                cell biology, gastrointestinal models

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