Morphophysiological Study of Gastrointestinal Tract of the Donkey (Equus Asinus) Arbab Sikandar
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Atoh8 Is a Regulator of Intestinal Microfold Cell (M Cell) Differentiation Joel Johnson George1, Laura Martin-Diaz1, Markus Ojanen1, Keijo Viiri1
bioRxiv preprint doi: https://doi.org/10.1101/2021.05.10.443378; this version posted May 10, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Atoh8 is a regulator of intestinal microfold cell (M cell) differentiation Joel Johnson George1, Laura Martin-Diaz1, Markus Ojanen1, Keijo Viiri1 1Faculty of Medicine and Health Technology, Tampere University Hospital, Tampere University Tampere, Finland. Grant Support: This work was supported by the Academy of Finland (no. 310011), Tekes (Business Finland) (no. 658/31/2015), Pediatric Research Foundation, Sigrid Jusélius Foundation, Mary och Georg C. Ehrnrooths Stiftelse, Laboratoriolääketieteen Edistämissäätiö sr. The funding sources played no role in the design or execution of this study or in the analysis and interpretation of the data. Abstract Intestinal microfold cells (M cells) are a dynamic lineage of epithelial cells that initiate mucosal immunity in the intestine. They are responsible for the uptake and transcytosis of microorganisms, pathogens and other antigens in the gastrointestinal tract. A mature M cell expresses a receptor Gp2 which binds to pathogens and aids in the uptake. Due to the rarity of these cells in the intestine, its development and differentiation remains yet to be fully understood. We recently demonstrated that polycomb repressive complex 2 (PRC2) is an epigenetic regulator of M cell development and 12 novel transcription factors including Atoh8 were revealed to be regulated by the PRC2. Here, we show that Atoh8 acts as a regulator of M cell differentiation; absence of Atoh8 led to a significant increase in the number of Gp2+ mature M cells and other M cell associated markers. -
Screening of Surface Markers on Rat Intestinal Mucosa Microfold Cells by Using Laser Capture Microdissection Combined with Protein Chip Technology
Int J Clin Exp Med 2014;7(4):932-939 www.ijcem.com /ISSN:1940-5901/IJCEM1401061 Original Article Screening of surface markers on rat intestinal mucosa microfold cells by using laser capture microdissection combined with protein chip technology Junyong Zhao*, Xiaoyu Li*, Qifeng Luo, Lei Xu, Lei Chen, Li Chai, Yixiang Huang, Lin Fang Department of Breast and Thyroid Surgery, Shanghai Tenth People’s Hospital, Tongji University, Shanghai, 200072, China. *Equal contributors. Received January 21, 2014; Accepted April 10, 2014; Epub April 15, 2014; Published April 30, 2014 Abstract: Objective: The objective of this research was to investigate the possibility of screening surface markers on rat intestinal mucosa microfold cells (M cells) by using laser capture microdissection (LCM) combined with protein chip technology. Methods: We labeled rat intestinal mucosa microfold cells with Ulex europaeus agglutinin (UEA)-1 antibody and visualized these by immunofluorescence staining. Using the Proteome Profiler rat protein chip, we analyzed the protein expression profiles of LCM M-cells compared to lymph follicle-associated epithelial (FAE) cells, and we identified potential differences to screen for marker proteins. Results: M cells can be clearly distinguished from lymphoid FAE cells under the fluorescence microscope. We successfully cut, isolated, and obtained microfold and lymph FAE cells with more than 95% homogeneity. Six differentially expressed proteins were identified through comparison of the protein chip profiles of these 2 cell types. Among these, VEGF, LIX, CNTF, and IL-1α/IL-1F1 were found to be at significantly lower levels in M cells, IL-1ra/IL-1F3 and MIG/CXCL9 appeared in significantly higher levels in M cells (P < 0.05). -
Digestive System Small and Large Intestines Lec. 21
Digestive System Small and Large Intestines Lec. 21 Histology Second year L. Hadeel Kamil 1 Small Intestine • The small intestine is a long, convoluted tube about 5 to 7 m long; it is the longest section of the digestive tract. The small intestine extends from the junction with the stomach to join with the large intestine or colon. For descriptive purposes, the small intestine is divided into three parts: the duodenum, jejunum, and ileum. Although the microscopic differences among these three segments are minor, they allow for identification of the segments. The main function of the small intestine is the digestion of gastric contents and absorption of nutrients into blood capillaries and lymphatic lacteals. 2 Surface Modifications of Small Intestine for Absorption • The mucosa of the small intestine exhibits specialized structural modifications that increase the cellular surface areas for absorption of nutrients and fluids. These modifications include the plicae circulares, villi, and microvilli. In contrast to the rugae of stomach, the plicae circulares are permanent spiral folds or elevations of the mucosa ( with a submucosal core) that extend into the intestinal lumen. The plicae circulares are most prominent in the proximal portion of the small intestine, where most absorption takes place; they decrease in prominence toward the ileum. Villi are permanent fingerlike projections of lamina propria of the mucosa that extend into the intestinal lumen. They are covered by simple columnar epithelium and are also more prominent in the proximal portion of the small intestine. The height of the villi decreases toward the ileum of the small intestine. The connective tissue core of each villus contains a lymphatic capillary called a lacteal, blood capillaries, and individual strands of smooth muscles 3 • Each villus has a core of lamina propria that is normally filled with blood vessels, lymphatic capillaries, nerves, smooth muscle, and loose irregular connective tissue. -
The Digestive System
69 chapter four THE DIGESTIVE SYSTEM THE DIGESTIVE SYSTEM The digestive system is structurally divided into two main parts: a long, winding tube that carries food through its length, and a series of supportive organs outside of the tube. The long tube is called the gastrointestinal (GI) tract. The GI tract extends from the mouth to the anus, and consists of the mouth, or oral cavity, the pharynx, the esophagus, the stomach, the small intestine, and the large intes- tine. It is here that the functions of mechanical digestion, chemical digestion, absorption of nutrients and water, and release of solid waste material take place. The supportive organs that lie outside the GI tract are known as accessory organs, and include the teeth, salivary glands, liver, gallbladder, and pancreas. Because most organs of the digestive system lie within body cavities, you will perform a dissection procedure that exposes the cavities before you begin identifying individual organs. You will also observe the cavities and their associated membranes before proceeding with your study of the digestive system. EXPOSING THE BODY CAVITIES should feel like the wall of a stretched balloon. With your skinned cat on its dorsal side, examine the cutting lines shown in Figure 4.1 and plan 2. Extend the cut laterally in both direc- out your dissection. Note that the numbers tions, roughly 4 inches, still working with indicate the sequence of the cutting procedure. your scissors. Cut in a curved pattern as Palpate the long, bony sternum and the softer, shown in Figure 4.1, which follows the cartilaginous xiphoid process to find the ventral contour of the diaphragm. -
Nomina Histologica Veterinaria, First Edition
NOMINA HISTOLOGICA VETERINARIA Submitted by the International Committee on Veterinary Histological Nomenclature (ICVHN) to the World Association of Veterinary Anatomists Published on the website of the World Association of Veterinary Anatomists www.wava-amav.org 2017 CONTENTS Introduction i Principles of term construction in N.H.V. iii Cytologia – Cytology 1 Textus epithelialis – Epithelial tissue 10 Textus connectivus – Connective tissue 13 Sanguis et Lympha – Blood and Lymph 17 Textus muscularis – Muscle tissue 19 Textus nervosus – Nerve tissue 20 Splanchnologia – Viscera 23 Systema digestorium – Digestive system 24 Systema respiratorium – Respiratory system 32 Systema urinarium – Urinary system 35 Organa genitalia masculina – Male genital system 38 Organa genitalia feminina – Female genital system 42 Systema endocrinum – Endocrine system 45 Systema cardiovasculare et lymphaticum [Angiologia] – Cardiovascular and lymphatic system 47 Systema nervosum – Nervous system 52 Receptores sensorii et Organa sensuum – Sensory receptors and Sense organs 58 Integumentum – Integument 64 INTRODUCTION The preparations leading to the publication of the present first edition of the Nomina Histologica Veterinaria has a long history spanning more than 50 years. Under the auspices of the World Association of Veterinary Anatomists (W.A.V.A.), the International Committee on Veterinary Anatomical Nomenclature (I.C.V.A.N.) appointed in Giessen, 1965, a Subcommittee on Histology and Embryology which started a working relation with the Subcommittee on Histology of the former International Anatomical Nomenclature Committee. In Mexico City, 1971, this Subcommittee presented a document entitled Nomina Histologica Veterinaria: A Working Draft as a basis for the continued work of the newly-appointed Subcommittee on Histological Nomenclature. This resulted in the editing of the Nomina Histologica Veterinaria: A Working Draft II (Toulouse, 1974), followed by preparations for publication of a Nomina Histologica Veterinaria. -
And Oropharynx-Associated Lymphoid Tissue of Sheep T ⁎ Vijay Kumar Saxenaa,B, Alejandra Diaza,C, Jean-Pierre Y
Veterinary Immunology and Immunopathology 208 (2019) 1–5 Contents lists available at ScienceDirect Veterinary Immunology and Immunopathology journal homepage: www.elsevier.com/locate/vetimm Identification and characterization of an M cell marker in nasopharynx- and oropharynx-associated lymphoid tissue of sheep T ⁎ Vijay Kumar Saxenaa,b, Alejandra Diaza,c, Jean-Pierre Y. Scheerlincka, a Centre for Animal Biotechnology, Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Victoria, 3010, Australia b Division of Animal Physiology and Biochemistry, ICAR-Central Sheep and Wool Research Institute, Avikanagar, Tonk, Rajasthan, 304501, India c Laboratorio de Inmunología, Departamento SAMP, Centro de Investigación Veterinaria de Tandil (CIVETAN-CONICET), Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Pcia. de Bs. As., Tandil, 7000, Buenos Aires, Argentina ARTICLE INFO ABSTRACT Keywords: M cells play a pivotal role in the induction of immune responses within the mucosa-associated lymphoid tissues. Sheep M cells exist principally in the follicle-associated epithelium (FAE) of the isolated solitary lymphoid follicles as M cells well as in the lymphoid follicles of nasopharynx-associated lymphoid tissue and gut associated lymphoid tissue NALT (GALT). Through lymphatic cannulation it is possible to investigate local immune responses induced following Mucosal immunity nasal Ag delivery in sheep. Hence, identifying sheep M cell markers would allow the targeting of M cells to offset Biomarker the problem of trans-epithelial Ag delivery associated with inducing mucosal immunity. Sheep cDNA from the GP2 tonsils of the oropharynx and nasopharynx was PCR amplified using Glycoprotein-2 (GP2)-specific primers and expressed as a poly-His-tagged recombinant sheep GP2 (56 kDa) in HEK293 cells. -
Digestive Tracttract
Digestive System ——DigestiveDigestive TractTract Dept.Dept. ofof HistologyHistology andand EmbryologyEmbryology 周莉周莉 教授教授 Introduction of digestive system * a long tube extending from the mouth to the anus, and associated with glands. * its main function: -digestion: physical/chemical -absorption * three major sections -the oral cavity including oropharynx -the tubular digestive tract -the major digestive glands: salivary glands, pancreas, liver, the general structure of the digestive tract Ⅰ. General Structure of the Digestive Tract 1. mucosa (1) epithelium: stratified squamous epithelium in two ends, the rest simple columnar epithelium (2) lamina propria: loose connective tissue rich in glands, lymphoid tissue and blood vessel (3) muscularis mucosa: thin layer of smooth muscle cells (innerinner circularcircular andand outerouter longitudinallongitudinal )) 2.2. SubmucosaSubmucosa:: CTCT,, esophagealesophageal glandsglands andand duodenumduodenum glandsglands,, submucosa(Meissnersubmucosa(Meissner)) nervenerve plexusplexus 3.3. muscularismuscularis:: innerinner circularcircular andand outerouter longitudinallongitudinal smoothsmooth musclemuscle cellscells myentericmyenteric nervenerve plexusplexus 4.4. Adventitia:Adventitia: fibrosafibrosa oror serosaserosa Ⅱ. The Oral Cavity 1.1. GeneralGeneral StructureStructure ofof MucosaMucosa ofof OralOral CavityCavity 2.2. tongue:tongue: mucosamucosa andand tonguetongue musclemuscle (( skeletalskeletal muscle)muscle) linguallingual papillaepapillae (1)(1) filiformfiliform papillaepapillae (2)(2) -
Materials for Oral Delivery of Proteins and Peptides
REVIEWS Materials for oral delivery of proteins and peptides Tyler D. Brown 1,2, Kathryn A. Whitehead 3,4 and Samir Mitragotri 1,2* Abstract | Throughout history , oral administration has been regarded as the most convenient mode of drug delivery , as it requires minimal expertise and invasiveness. Although oral delivery works well for small-molecule drugs, oral delivery of macromolecules (particularly proteins and peptides) has been limited by acidic conditions in the stomach and low permeability across the intestinal epithelium. Accordingly , the large numbers of biologic drugs that have become available in the past 10 years typically require administration by injection or infusion. As such, a renewed emphasis has been placed on the development of novel materials that overcome the physiological challenges of oral delivery for macromolecular agents. This Review provides an overview of physiological barriers to the oral delivery of biologics and highlights the advances made in materials across various length scales, from small molecules to macroscopic devices. This Review also describes the current status of materials for oral delivery of protein and peptide drugs. The past decade has seen an increase in the number route13. Unfortunately, barring some very small pep of new drugs approved by the US Food and Drug Admin tides such as ciclosporin, oral delivery is not a currently istration (FDA), leading to an all time record number available option for protein and antibody drugs14. These of 59 novel drug approvals in 2018. Drugs for oral use macro molecular agents have prohibitively low oral bio continue to dominate the therapeutic landscape, encom availability due to several features of the gastrointestinal passing over 50% of these approvals1. -
Bacteria Slides
BACTERIA SLIDES Cocci Bacillus BACTERIA SLIDES _______________ __ BACTERIA SLIDES Spirilla BACTERIA SLIDES ___________________ _____ BACTERIA SLIDES Bacillus BACTERIA SLIDES ________________ _ LUNG SLIDE Bronchiole Lumen Alveolar Sac Alveoli Alveolar Duct LUNG SLIDE SAGITTAL SECTION OF HUMAN HEAD MODEL Superior Concha Auditory Tube Middle Concha Opening Inferior Concha Nasal Cavity Internal Nare External Nare Hard Palate Pharyngeal Oral Cavity Tonsils Tongue Nasopharynx Soft Palate Oropharynx Uvula Laryngopharynx Palatine Tonsils Lingual Tonsils Epiglottis False Vocal Cords True Vocal Cords Esophagus Thyroid Cartilage Trachea Cricoid Cartilage SAGITTAL SECTION OF HUMAN HEAD MODEL LARYNX MODEL Side View Anterior View Hyoid Bone Superior Horn Thyroid Cartilage Inferior Horn Thyroid Gland Cricoid Cartilage Trachea Tracheal Rings LARYNX MODEL Posterior View Epiglottis Hyoid Bone Vocal Cords Epiglottis Corniculate Cartilage Arytenoid Cartilage Cricoid Cartilage Thyroid Gland Parathyroid Glands LARYNX MODEL Side View Anterior View ____________ _ ____________ _______ ______________ _____ _____________ ____________________ _____ ______________ _____ _________ _________ ____________ _______ LARYNX MODEL Posterior View HUMAN HEART & LUNGS MODEL Larynx Tracheal Rings Found on the Trachea Left Superior Lobe Left Inferior Lobe Heart Right Superior Lobe Right Middle Lobe Right Inferior Lobe Diaphragm HUMAN HEART & LUNGS MODEL Hilum (curvature where blood vessels enter lungs) Carina Pulmonary Arteries (Blue) Pulmonary Veins (Red) Bronchioles Apex (points -
Cells: Important Immunosurveillance Posts in the Intestinal Epithelium Neil A
Microfold (M) cells: important immunosurveillance posts in the intestinal epithelium Neil A. Mabbott, University of Edinburgh David S. Donaldson, University of Edinburgh Hiroshi Ohno, Research Center for Allergy and Immunology, Japan Ifor Williams, Emory University Arvind Mahajan, University of Edinburgh Journal Title: Mucosal Immunology Volume: Volume 6, Number 4 Publisher: Nature Publishing Group | 2013-07-01, Pages 666-677 Type of Work: Article | Post-print: After Peer Review Publisher DOI: 10.1038/mi.2013.30 Permanent URL: https://pid.emory.edu/ark:/25593/vhq2b Final published version: http://dx.doi.org/10.1038/mi.2013.30 Copyright information: © 2021 Springer Nature Limited Accessed September 28, 2021 6:58 PM EDT Europe PMC Funders Group Author Manuscript Mucosal Immunol. Author manuscript; available in PMC 2013 July 01. Published in final edited form as: Mucosal Immunol. 2013 July ; 6(4): 666–677. doi:10.1038/mi.2013.30. Europe PMC Funders Author Manuscripts Microfold (M) cells: important immunosurveillance posts in the intestinal epithelium Neil A. Mabbott1,#, David S. Donaldson1, Hiroshi Ohno2, Ifor R. Williams3, and Arvind Mahajan1 1The Roslin Institute & Royal (Dick) School of Veterinary Sciences, University of Edinburgh, United Kingdom 2Research Center for Allergy and Immunology (RCAI), RIKEN, 1-7-22 Suehiro, Tsurumi, Yokohama 230-0045, Japan 3Department of Pathology, Emory University School of Medicine, Whitehead Bldg. 105D, 615 Michael St., Atlanta, GA 30322, USA SUMMARY The transcytosis of antigens across the gut epithelium by microfold cells (M cells) is important for the induction of efficient immune responses to some mucosal antigens in Peyer’s patches. Recently, substantial progress has been made in our understanding of the factors that influence the development and function of M cells. -
Oral Recombinant Lactobacillus Vaccine Targeting the Intestinal
Ma et al. Microb Cell Fact (2018) 17:20 https://doi.org/10.1186/s12934-018-0861-7 Microbial Cell Factories RESEARCH Open Access Oral recombinant Lactobacillus vaccine targeting the intestinal microfold cells and dendritic cells for delivering the core neutralizing epitope of porcine epidemic diarrhea virus Sunting Ma1†, Li Wang1†, Xuewei Huang1, Xiaona Wang1, Su Chen1, Wen Shi1, Xinyuan Qiao1,2, Yanping Jiang1, Lijie Tang1,2, Yigang Xu1,2* and Yijing Li1,2* Abstract Background: Porcine epidemic diarrhea caused by porcine epidemic diarrhea virus (PEDV) has led to serious eco- nomic losses to the swine industry worldwide. In this study, an oral recombinant Lactobacillus casei vaccine against PEDV infection targeting the intestinal microfold (M) cells and dendritic cells (DCs) for delivering the core neutralizing epitope (COE) of PEDV spike protein was developed with M cell-targeting peptide (Col) and dendritic cell-targeting peptide (DCpep). The immunogenicity of the orally administered recombinant strains was evaluated. Results: After immunization, signifcantly higher levels of anti-PEDV specifc IgG antibodies with PEDV neutralizing activity in the sera and mucosal sIgA antibodies in the tractus genitalis, intestinal mucus, and stools were detected in mice orally administered with the recombinant strain pPG-COE-Col-DCpep/L393, which expressed DCpep and Col targeting ligands fused with the PEDV COE antigen, compared to mice orally immunized with the recombinant strain pPG-COE/L393 without the DCpep and Col targeting ligands. Moreover, in response to restimulation with the PEDV COE antigen in vitro, a signifcant diference in splenocyte proliferation response and Th2-associated cytokine IL-4 level was observed in the group of mice orally immunized with pPG-COE-Col-DCpep/L393 (p < 0.05) compared to the groups of mice that received pPG-COE-Col/L393 and pPG-COE-DCpep/L393, respectively. -
Clonal Transitions and Phenotypic Evolution in Barrett Esophagus
medRxiv preprint doi: https://doi.org/10.1101/2021.03.31.21252894; this version posted April 6, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission. 1 Clonal transitions and phenotypic evolution in Barrett esophagus Short title: Phenotypic evolution in Barrett esophagus James A Evans1*, Emanuela Carlotti1*, Meng-Lay Lin1, Richard J Hackett1, Adam Passman1, , Lorna Dunn2§, George Elia1, Ross J Porter3#, Mairi H McClean3**, Frances Hughes4, Joanne ChinAleong5, Philip Woodland6, Sean L Preston6, S Michael Griffin2,7, Laurence Lovat8, Manuel Rodriguez-Justo9, Nicholas A Wright1, Marnix Jansen10,11 & Stuart AC McDonald1 1Clonal dynamics in epithelia laboratory, 3Epithelial stem cell laboratory, Centre for Cancer Genomics and Computational Biology, Barts Cancer Institute, Queen Mary University of London, London, UK 2Nothern Institute for Cancer Research, Newcastle University, Newcastle, UK 3Department of Gastroenterology, University of Aberdeen, Aberdeen, UK 4Department of Surgery, 5Histopathology, 6Endoscopy Unit, Barts Health NHS Trust, Royal London Hospital, London, UK 7Royal College of Surgeons of Edinburgh, Edinburgh, UK 8Oeosophagogastric Disorders Centre, Department of Gastroenterology, University College London Hospitals, London, UK 9Research Department of Tissue and Energy, UCL Division of Surgical and Interventional Science, University College London