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      Gestational Exposure to Cigarette Smoke Suppresses the Gasotransmitter H 2S Biogenesis and the Effects Are Transmitted Transgenerationally

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          Abstract

          Rationale: Gestational cigarette smoke (CS) impairs lung angiogenesis and alveolarization, promoting transgenerational development of asthma and bronchopulmonary dysplasia (BPD). Hydrogen sulfide (H 2S), a proangiogenic, pro-alveolarization, and anti-asthmatic gasotransmitter is synthesized by cystathionine-γ-lyase (CSE), cystathionine-β-synthase (CBS), and 3-mercaptopyruvate sulfur transferase (3MST).

          Objective: Determine if gestational CS exposure affected the expression of H 2S synthesizing enzymes in the mouse lung and human placenta.

          Methods: Mice were exposed throughout gestational period to secondhand CS (SS) at approximating the dose of CS received by a pregnant woman sitting in a smoking bar for 3 h/days during pregnancy. Lungs from 7-days old control and SS-exposed pups and human placenta from mothers who were either non-smokers or smokers during pregnancy were analyzed for expression of the enzymes.

          Measurements: Mouse lungs and human placentas were examined for the expression of CSE, CBS, and 3MST by immunohistochemical staining, qRT-PCR and/or Western blot (WB) analyses.

          Results: Compared to controls, mouse lung exposed gestationally to SS had significantly lower levels of CSE, CBS, and 3MST. Moreover, the SS-induced suppression of CSE and CBS in F1 lungs was transmitted to the F2 generation without significant change in the magnitude of the suppression. These changes were associated with impaired epithelial-mesenchymal transition (EMT)—a process required for normal lung angiogenesis and alveolarization. Additionally, the placentas from mothers who smoked during pregnancy, expressed significantly lower levels of CSE, CBS, and 3MST, and the effects were partially moderated by quitting smoking during the first trimester.

          Conclusions: Lung H 2S synthesizing enzymes are downregulated by gestational CS and the effects are transmitted to F2 progeny. Smoking during pregnancy decreases H 2S synthesizing enzymes is human placentas, which may correlate with the increased risk of asthma/BPD in children.

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          Most cited references65

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          Preparing for the first breath: genetic and cellular mechanisms in lung development.

          The mammalian respiratory system--the trachea and the lungs--arises from the anterior foregut through a sequence of morphogenetic events involving reciprocal endodermal-mesodermal interactions. The lung itself consists of two highly branched, tree-like systems--the airways and the vasculature--that develop in a coordinated way from the primary bud stage to the generation of millions of alveolar gas exchange units. We are beginning to understand some of the molecular and cellular mechanisms that underlie critical processes such as branching morphogenesis, vascular development, and the differentiation of multipotent progenitor populations. Nevertheless, many gaps remain in our knowledge, the filling of which is essential for understanding respiratory disorders, congenital defects in human neonates, and how the disruption of morphogenetic programs early in lung development can lead to deficiencies that persist throughout life. (c) 2010 Elsevier Inc. All rights reserved.
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            The possible role of hydrogen sulfide as an endogenous smooth muscle relaxant in synergy with nitric oxide.

            Hydrogen sulfide (H2S), which is well known as a toxic gas, is produced endogenously in mammalian tissues from L-cysteine mainly by two pyridoxal-5'-phosphate-dependent enzymes, cystathionine beta-synthetase and cystathionine gamma-lyase. Recently, we showed that cystathionine beta-synthetase in the brain produces H2S, and that H2S facilitates the induction of hippocampal long-term potentiation by enhancing NMDA receptor activity. Here we show that mRNA for another H2S producing enzyme, cystathionine gamma-lyase, is expressed in the ileum, portal vein, and thoracic aorta. The ileum also expresses cystathionine beta-synthetase mRNA. These tissues produce H2S, and this production is blocked by cystathionine beta-synthetase and cystathionine gamma-lyase specific inhibitors. Although exogenously applied H2S alone relaxed these smooth muscles, much lower concentrations of H2S greatly enhanced the smooth muscle relaxation induced by NO in the thoracic aorta. These observations suggest that the endogenous H2S may regulate smooth muscle tone in synergy with NO.
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              Hydrogen sulfide: its production, release and functions.

              Hydrogen sulfide (H(2)S), which is a well-known toxic gas, has been recognized as a signal molecule as well as a cytoprotectant. It is produced by three enzymes, cystathionine β-synthase, cystathionine γ-lyase and 3-mercaptopyruvate sulfurtransferase along with cysteine aminotransferase. In addition to an immediate release of H(2)S from producing enzymes, it can be stored as bound sulfane sulfur, which may release H(2)S in response to physiological stimuli. As a signal molecule, it modulates neuronal transmission, relaxes smooth muscle, regulates release of insulin and is involved in inflammation. Because of its reputation as a toxic gas, the function as a cytoprotectant has been overlooked: the nervous system and cardiovascular system are protected from oxidative stress. In this review, enzymatic production, release mechanism and functions of H(2)S are focused on.
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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
                28 July 2020
                2020
                : 11
                : 1628
                Affiliations
                [1] 1Respiratory Immunology Division, Lovelace Respiratory Research Institute , Albuquerque, NM, United States
                [2] 2Department of Immunology and Nanomedicine, Herbert Wertheim College of Medicine, Florida International University , Miami, FL, United States
                [3] 3Department of Microbiology and Immunology , Galveston, TX, United States
                [4] 4Department of Pediatrics, University of New Mexico Health Sciences Center , Albuquerque, NM, United States
                Author notes

                Edited by: Christian Herr, Saarland University Hospital, Germany

                Reviewed by: Tanima Bose, Ludwig Maximilian University of Munich, Germany; Irene Marafini, Policlinico Tor Vergata, Italy

                *Correspondence: Mohan L. Sopori msopori@ 123456lrri.org

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

                Article
                10.3389/fimmu.2020.01628
                7399059
                218b83b6-19a1-42b9-97fb-a239f66881eb
                Copyright © 2020 Singh, Devadoss, Manevski, Sheybani, Ivanciuc, Exil, Agarwal, Raizada, Garofalo, Chand and Sopori.

                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
                : 28 February 2020
                : 17 June 2020
                Page count
                Figures: 5, Tables: 0, Equations: 0, References: 75, Pages: 12, Words: 7331
                Categories
                Immunology
                Original Research

                Immunology
                gestational cigarette smoke,h2s biogenesis,human placenta,lungs,transgenerational effect

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