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      Notch Signaling Pathway Expression in the Skin of Leprosy Patients: Association With Skin and Neural Damage

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          Abstract

          Introduction: Leprosy is an infectious disease caused by Mycobacterium leprae, a debilitating disease that affects the skin and peripheral nerves. It is possible that tissue changes during infection with leprosy are related to alterations in the activity of the Notch signaling pathway, an innate signaling pathway in the physiology of the skin and peripheral nerves.

          Methods: This is a descriptive observational study. Thirty skin biopsies from leprosy patients and 15 from individuals with no history of this disease were evaluated. In these samples, gene expressions of cellular components associated with the Notch signaling pathway, Hes-1, Hey-1, Runx-1 Jagged-1, Notch-1, and Numb, were evaluated using q-PCR, and protein expression was evaluated using immunohistochemistry of Runx-1 and Hes-1.

          Results: Changes were observed in the transcription of Notch signaling pathway components; Hes-1 was downregulated and Runx-1 upregulated in the skin of infected patients. These results were confirmed by immunohistochemistry, where reduction of Hes-1 expression was found in the epidermis, eccrine glands, and hair follicles. Increased expression of Runx-1 was found in inflammatory cells in the dermis of infected patients; however, it is not related to tissue changes. With these results, a multivariate analysis was performed to determine the causes of transcription factor Hes-1 reduction. It was concluded that tissue inflammation was the main cause.

          Conclusions: The tissue changes found in the skin of infected patients could be associated with a reduction in the expression of Hes-1, a situation that would promote the survival and proliferation of M. leprae in this tissue.

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          Most cited references29

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          Canonical notch signaling functions as a commitment switch in the epidermal lineage.

          Mammalian epidermis consists of a basal layer of proliferative progenitors that gives rise to multiple differentiating layers to provide a waterproof envelope covering the skin surface. To accomplish this, progenitor cells must detach from the basal layer, move upward, and execute a terminal differentiation program consisting of three distinct stages: spinous, granular layer, and stratum corneum. Notch signaling has been implicated in late stages of differentiation, but the commitment switch remains unknown. Here we show with loss and gain-of-function studies that active Notch intracellular domain (NICD) and its obligate canonical signaling partner RBP-J act at the basal/suprabasal juncture to induce spinous and down-regulate basal fate. Spinous layers are absent in RBP-J conditional null epidermis and expanded when Notch1 signaling is elevated transgenically in epidermis. We show that RBP-J is essential for mediating both spinous gene activation and basal gene repression. In contrast, the NICD/RBP-J target gene Hes1 is expressed in spinous layers and mediates spinous gene induction but not basal gene repression. These data uncover an early role for RBP-J and Notch in commitment of epidermal cells to terminally differentiate and reveal that spinous gene induction is mediated by a Hes1-dependent mechanism, while basal gene repression occurs independently of Hes1.
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            Sweat gland progenitors in development, homeostasis, and wound repair.

            The human body is covered with several million sweat glands. These tiny coiled tubular skin appendages produce the sweat that is our primary source of cooling and hydration of the skin. Numerous studies have been published on their morphology and physiology. Until recently, however, little was known about how glandular skin maintains homeostasis and repairs itself after tissue injury. Here, we provide a brief overview of sweat gland biology, including newly identified reservoirs of stem cells in glandular skin and their activation in response to different types of injuries. Finally, we discuss how the genetics and biology of glandular skin has advanced our knowledge of human disorders associated with altered sweat gland activity.
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              Multiple roles of Notch signaling in the regulation of epidermal development.

              Recent studies have shown that Notch signaling plays an important role in epidermal development, but the underlying molecular mechanisms remain unclear. Here, by integrating loss- and gain-of-function studies of Notch receptors and Hes1, we describe molecular information about the role of Notch signaling in epidermal development. We show that Notch signaling determines spinous cell fate and induces terminal differentiation by a mechanism independent of Hes1, but Hes1 is required for maintenance of the immature state of spinous cells. Notch signaling induces Ascl2 expression to promote terminal differentiation, while simultaneously repressing Ascl2 through Hes1 to inhibit premature terminal differentiation. Despite the critical role of Hes1 in epidermal development, Hes1 null epidermis transplanted to adult mice showed no obvious defects, suggesting that this role of Hes1 may be restricted to developmental stages. Overall, we conclude that Notch signaling orchestrates the balance between differentiation and immature programs in suprabasal cells during epidermal development.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                19 March 2020
                2020
                : 11
                : 368
                Affiliations
                [1] 1Grupo de Ciencias Básicas, Doctorado en Ciencias de la Salud, Escuela de Graduados, Universidad CES , Medellín, Colombia
                [2] 2Línea de Investigación en Lepra, Instituto Colombiano de Medicina Tropical, Universidad CES , Medellín, Colombia
                [3] 3Laboratorio de Dermatopatología, Centro de Investigaciones en Dermatología (CIDERM), Facultad de Medicina, Universidad de Antioquia , Medellín, Colombia
                Author notes

                Edited by: Malcolm Scott Duthie, HDT Biotech Corporation, United States

                Reviewed by: Patricia Sammarco Rosa, Instituto Lauro de Souza Lima, Brazil; Mirian Nacagami Sotto, University of São Paulo, Brazil

                *Correspondence: Héctor Serrano-Coll serrano.hector@ 123456uces.edu.co
                Nora Cardona-Castro ncardona@ 123456ces.edu.co

                This article was submitted to Microbial Immunology, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2020.00368
                7096478
                bb278305-d79b-47c9-af69-4cba16765762
                Copyright © 2020 Serrano-Coll, Ospina, Salazar-Peláez and Cardona-Castro.

                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
                : 12 December 2019
                : 17 February 2020
                Page count
                Figures: 9, Tables: 6, Equations: 0, References: 43, Pages: 17, Words: 9261
                Funding
                Funded by: Departamento Administrativo de Ciencia, Tecnología e Innovación (COLCIENCIAS) 10.13039/100007637
                Award ID: 727-2015
                Categories
                Immunology
                Original Research

                Immunology
                mycobacterium leprae,hes-1 transcription factor,runx-1 transcription factor,inflammation,epidermis,hair follicle,eccrine gland,nerve fiber

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