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      The Role of Innate Immune System in the Human Amniotic Membrane and Human Amniotic Fluid in Protection Against Intra-Amniotic Infections and Inflammation

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          Abstract

          Intra-amniotic infection and inflammation (IAI) affect fetal development and are highly associated with preterm labor and premature rupture of membranes, which often lead to adverse neonatal outcomes. Human amniotic membrane (hAM), the inner part of the amnio-chorionic membrane, protects the embryo/fetus from environmental dangers, including microbial infection. However, weakened amnio-chorionic membrane may be breached or pathogens may enter through a different route, leading to IAI. The hAM and human amniotic fluid (hAF) respond by activation of all components of the innate immune system. This includes changes in 1) hAM structure, 2) presence of immune cells, 3) pattern recognition receptors, 4) cytokines, 5) antimicrobial peptides, 6) lipid derivatives, and 7) complement system. Herein we provide a comprehensive and integrative review of the current understanding of the innate immune response in the hAM and hAF, which will aid in design of novel studies that may lead to breakthroughs in how we perceive the IAI.

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          Most cited references291

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          Cleavage of GSDMD by inflammatory caspases determines pyroptotic cell death.

          Inflammatory caspases (caspase-1, -4, -5 and -11) are critical for innate defences. Caspase-1 is activated by ligands of various canonical inflammasomes, and caspase-4, -5 and -11 directly recognize bacterial lipopolysaccharide, both of which trigger pyroptosis. Despite the crucial role in immunity and endotoxic shock, the mechanism for pyroptosis induction by inflammatory caspases is unknown. Here we identify gasdermin D (Gsdmd) by genome-wide clustered regularly interspaced palindromic repeat (CRISPR)-Cas9 nuclease screens of caspase-11- and caspase-1-mediated pyroptosis in mouse bone marrow macrophages. GSDMD-deficient cells resisted the induction of pyroptosis by cytosolic lipopolysaccharide and known canonical inflammasome ligands. Interleukin-1β release was also diminished in Gsdmd(-/-) cells, despite intact processing by caspase-1. Caspase-1 and caspase-4/5/11 specifically cleaved the linker between the amino-terminal gasdermin-N and carboxy-terminal gasdermin-C domains in GSDMD, which was required and sufficient for pyroptosis. The cleavage released the intramolecular inhibition on the gasdermin-N domain that showed intrinsic pyroptosis-inducing activity. Other gasdermin family members were not cleaved by inflammatory caspases but shared the autoinhibition; gain-of-function mutations in Gsdma3 that cause alopecia and skin defects disrupted the autoinhibition, allowing its gasdermin-N domain to trigger pyroptosis. These findings offer insight into inflammasome-mediated immunity/diseases and also change our understanding of pyroptosis and programmed necrosis.
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            Pattern recognition receptors and inflammation.

            Infection of cells by microorganisms activates the inflammatory response. The initial sensing of infection is mediated by innate pattern recognition receptors (PRRs), which include Toll-like receptors, RIG-I-like receptors, NOD-like receptors, and C-type lectin receptors. The intracellular signaling cascades triggered by these PRRs lead to transcriptional expression of inflammatory mediators that coordinate the elimination of pathogens and infected cells. However, aberrant activation of this system leads to immunodeficiency, septic shock, or induction of autoimmunity. In this Review, we discuss the role of PRRs, their signaling pathways, and how they control inflammatory responses. 2010 Elsevier Inc. All rights reserved.
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              Neutrophil extracellular traps in immunity and disease

              Neutrophils are innate immune phagocytes that have a central role in immune defence. Our understanding of the role of neutrophils in pathogen clearance, immune regulation and disease pathology has advanced dramatically in recent years. Web-like chromatin structures known as neutrophil extracellular traps (NETs) have been at the forefront of this renewed interest in neutrophil biology. The identification of molecules that modulate the release of NETs has helped to refine our view of the role of NETs in immune protection, inflammatory and autoimmune diseases and cancer. Here, I discuss the key findings and concepts that have thus far shaped the field of NET biology.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/1340901
                URI : https://loop.frontiersin.org/people/550332
                URI : https://loop.frontiersin.org/people/463631
                URI : https://loop.frontiersin.org/people/780438
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                21 October 2021
                2021
                : 12
                : 735324
                Affiliations
                [1] 1 Department of Synthetic Biology and Immunology, National Institute of Chemistry , Ljubljana, Slovenia
                [2] 2 Institute of Cell Biology, Faculty of Medicine, University of Ljubljana , Ljubljana, Slovenia
                [3] 3 Department of Biology, Biotechnical Faculty, University of Ljubljana , Ljubljana, Slovenia
                Author notes

                Edited by: Harry D. Dawson, Agricultural Research Service (USDA), United States

                Reviewed by: Pietro Presicce, UCLA Department of Pediatrics, United States; Lauren Stafford Richardson, University of Texas Medical Branch at Galveston, United States

                *Correspondence: Mateja Erdani Kreft, mateja.erdani@ 123456mf.uni-lj.si ; Marjanca Starčič Erjavec, marjanca.starcic.erjavec@ 123456bf.uni-lj.si

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

                Article
                10.3389/fimmu.2021.735324
                8566738
                34745106
                69040ad7-0643-479d-ad0b-244f8296e6dc
                Copyright © 2021 Šket, Ramuta, Starčič Erjavec and Kreft

                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
                : 02 July 2021
                : 23 September 2021
                Page count
                Figures: 2, Tables: 1, Equations: 0, References: 293, Pages: 18, Words: 7064
                Funding
                Funded by: Javna Agencija za Raziskovalno Dejavnost RS , doi 10.13039/501100004329;
                Funded by: Javna Agencija za Raziskovalno Dejavnost RS , doi 10.13039/501100004329;
                Categories
                Immunology
                Review

                Immunology
                human amniotic membrane,placenta,intrauterine infection,innate immune system,antimicrobial activity,bacteria,preterm birth

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