Lecture12 Genmed 2Nd Semester
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Characterization of Murine Macrophages from Bone Marrow
Wang et al. BMC Immunology 2013, 14:6 http://www.biomedcentral.com/1471-2172/14/6 RESEARCH ARTICLE Open Access Characterization of murine macrophages from bone marrow, spleen and peritoneum Changqi Wang1*†, Xiao Yu1,2†, Qi Cao1, Ya Wang1, Guoping Zheng1, Thian Kui Tan1, Hong Zhao1,3, Ye Zhao1, Yiping Wang1 and David CH Harris1 Abstract Background: Macrophages have heterogeneous phenotypes and complex functions within both innate and adaptive immune responses. To date, most experimental studies have been performed on macrophages derived from bone marrow, spleen and peritoneum. However, differences among macrophages from these particular sources remain unclear. In this study, the features of murine macrophages from bone marrow, spleen and peritoneum were compared. Results: We found that peritoneal macrophages (PMs) appear to be more mature than bone marrow derived macrophages (BMs) and splenic macrophages (SPMs) based on their morphology and surface molecular characteristics. BMs showed the strongest capacity for both proliferation and phagocytosis among the three populations of macrophage. Under resting conditions, SPMs maintained high levels of pro-inflammatory cytokines expression (IL-6, IL-12 and TNF-α), whereas BMs produced high levels of suppressive cytokines (IL-10 and TGF-β). However, SPMs activated with LPS not only maintained higher levels of (IL-6, IL-12 and TNF-α) than BMs or PMs, but also maintained higher levels of IL-10 and TGF-β. Conclusions: Our results show that BMs, SPMs and PMs are distinct populations with different biological functions, providing clues to guide their further experimental or therapeutic use. Keywords: Macrophage, Bone marrow, Spleen, Peritoneum Background macrophage populations could be attributed to their het- Macrophages play an essential role in both innate and erogeneity [4]. -
Pulp Border in L1-Deficient Mice Selective Malformation of the Splenic White
Selective Malformation of the Splenic White Pulp Border in L1-Deficient Mice Shih-Lien Wang, Michael Kutsche, Gino DiSciullo, Melitta Schachner and Steven A. Bogen This information is current as of September 27, 2021. J Immunol 2000; 165:2465-2473; ; doi: 10.4049/jimmunol.165.5.2465 http://www.jimmunol.org/content/165/5/2465 Downloaded from References This article cites 45 articles, 12 of which you can access for free at: http://www.jimmunol.org/content/165/5/2465.full#ref-list-1 Why The JI? Submit online. http://www.jimmunol.org/ • Rapid Reviews! 30 days* from submission to initial decision • No Triage! Every submission reviewed by practicing scientists • Fast Publication! 4 weeks from acceptance to publication *average by guest on September 27, 2021 Subscription Information about subscribing to The Journal of Immunology is online at: http://jimmunol.org/subscription Permissions Submit copyright permission requests at: http://www.aai.org/About/Publications/JI/copyright.html Email Alerts Receive free email-alerts when new articles cite this article. Sign up at: http://jimmunol.org/alerts The Journal of Immunology is published twice each month by The American Association of Immunologists, Inc., 1451 Rockville Pike, Suite 650, Rockville, MD 20852 Copyright © 2000 by The American Association of Immunologists All rights reserved. Print ISSN: 0022-1767 Online ISSN: 1550-6606. Selective Malformation of the Splenic White Pulp Border in L1-Deficient Mice1 Shih-Lien Wang,* Michael Kutsche,† Gino DiSciullo,* Melitta Schachner,† and Steven A. Bogen2* Lymphocytes enter the splenic white pulp by crossing the poorly characterized boundary of the marginal sinus. In this study, we describe the importance of L1, an adhesion molecule of the Ig superfamily, for marginal sinus integrity. -
USC 591.4: 591.441: 597/599 MORPHOLOGICAL FEATURES of the SPLENIC RED PULP Ph.D. in Biological Sciences, Associate Professor, Du
INNOVATIVE SOLUTIONS IN MODERN SCIENCE № 4 (4), 2016 USC 591.4: 591.441: 597/599 MORPHOLOGICAL FEATURES OF THE SPLENIC RED PULP Ph.D. in Biological Sciences, associate professor, Dunaievska O. F. Zhytomyr National Agroecological University, Ukraine, Zhytomyr The spleen is an important peripheral organ of the sanguification and immune defense. In vertebrates and humans, it is formed by the support- contractile apparatus, as well as by the white and red pulps. The red pulp consists of the soft splenic cords, reticular stromal systems, and sinuses, including vascular structures. The relative area of red pulp is an important test criterion of the organ. It takes from 48,95% to 84,3% in the vertebrates, and from 71,4% to 83,6% in humans. It depends on the class, type, race, sex, breed, the age of animals, or the person's age and physiological state. The indicator of red pulp’s relative area is used as a biomarker in the environment bioindication. Any change of its values indicates the changes of the environmental conditions. Determination of the morphological standards in the organs and tissues according to the animals’ age, species, and breed aspects is used in the prevention of diseases, effective treatment, and getting the high-quality food. The test criteria of the spleen are important while studying the effect of pharmacological drugs, conditions of animal sustentation and feeding. Determination of splenic morphometric parameters is of the great practical importance, particularly in surgery, laboratory diagnostics, and development of the medical measures. Keywords: spleen, morphology, fish, frogs, birds, mammals, human. Spleen belongs to the peripheral organ of the sanguification and immune protection; it is presented in all vertebrates. -
201028 the Lymphatic System 2 – Structure and Function of The
Copyright EMAP Publishing 2020 This article is not for distribution except for journal club use Clinical Practice Keywords Immunity/Anatomy/Stem cell production/Lymphatic system Systems of life This article has been Lymphatic system double-blind peer reviewed In this article... l How blood and immune cells are produced and developed by the lymphatic system l Clinical significance of the primary and secondary lymphoid organs l How the lymphatic system mounts an immune response and filters pathogens The lymphatic system 2: structure and function of the lymphoid organs Key points Authors Yamni Nigam is professor in biomedical science; John Knight is associate The lymphoid professor in biomedical science; both at the College of Human and Health Sciences, organs include the Swansea University. red bone marrow, thymus, spleen Abstract This article is the second in a six-part series about the lymphatic system. It and clusters of discusses the role of the lymphoid organs, which is to develop and provide immunity lymph nodes for the body. The primary lymphoid organs are the red bone marrow, in which blood and immune cells are produced, and the thymus, where T-lymphocytes mature. The Blood and immune lymph nodes and spleen are the major secondary lymphoid organs; they filter out cells are produced pathogens and maintain the population of mature lymphocytes. inside the red bone marrow, during a Citation Nigam Y, Knight J (2020) The lymphatic system 2: structure and function of process called the lymphoid organs. Nursing Times [online]; 116: 11, 44-48. haematopoiesis The thymus secretes his article discusses the major become either erythrocytes, leucocytes or hormones that are lymphoid organs and their role platelets. -
1 | Page: Immune Cells and Tissues Swailes Cells and Tissues of The
Cells and Tissues of the Immune System N. Swailes, Ph.D. Department of Anatomy and Cell Biology Rm: B046A ML Tel: 5-7726 E-mail: [email protected] Required reading Mescher AL, Junqueira’s Basic Histology Text and Atlas, 12th Edition, Chapter 20: pp226-2480 Ross MH and Pawlina W, Histology: A text and Atlas, 6th Edition, Chapter 21: pp396-429 Learning objectives 1) Identify the major cells of the immune system and briefly outline their function 2) Describe the general structure of lymphoid tissue 3) Differentiate between primary and secondary immune organs 4) Identify the thymus and discuss the role of its cells in ‘educating’ immature T-cells 5) Identify a lymph node and outline how an immune response is triggered here 6) Identify the spleen and describe the role of red and white pulp in filtering the blood and reacting to blood borne antigens 7) Differentiate between MALT in the oral cavity (tonsils) 8) Know where to find and how to identify examples of BALT and GALT Major Take Home Points A. Lymphoid tissues are composed of different types of lymphocytes and supporting cells within a scaffold of Type III collagen/reticular fibers B. The major primary lymphoid organs are encapsulated organs where immature lymphocytes are born (bone marrow) and become immunocompetent (thymus) C. The major secondary lymphoid organs are encapsulated organs where immunocompetent lymphocytes differentiate into effector cells after exposure to antigen in the blood (spleen) or lymph (nodes) D. Mucosa Associated Lymphoid Tissues (MALT) are un-encapsulated areas of lymphoid tissue within the mucosa of organs that can be identified by their lining epithelium (tonsils, GALT: ileum and appendix, BALT) 1 | Page: Immune Cells and Tissues Swailes A1: Organization of the immune system 5a A. -
Innate-, Adaptive- and Natural Immunity
Basic Immunology (Dentistry) Lecture 1. Introduction, phylogenesis of the immune system (innate-, adaptive- and natural immunity). Ferenc Boldizsar MD, PhD Introducing the subject 1. • Please follow our website www.immbio.hu through the whole semester for up-to-date informations about our education. • Student preparation and learning will be controlled with the help of the www.medtraining.eu website. At the beginning of the semester all students will be registered automatically with their specific neptun codes. After activation you will use this platform for completing the weekly tests as well as the exam test. Login Name: neptun code Password: neptun code Introducing the subject 2. • 2 lectures / week (preparation of own lecture notes!) Name list will be led every week. Maximum 3 absences allowed! • Lecture tests: quick tests at the beginning of the lectures (first 10 minutes) from the previous week’s lectures (2 randomized test questions in medtraining system). 12 tests for 2 points for a max. of 24 points. For the acceptance of the semester a min. of 50% (12 points) must be collected. Points above 12 will be added to the exam test points. • Exam: online test exam in medtraining system from the lectures. Evaluation: minimum level: 66%; satisfactory 66- 71%, average 72- 77%, good 78-83%, excellent 84% • Website: www.immbio.hu University of Pécs, Medical School, Department of Immunology and Biotechnology Director: Prof. Dr. Timea Berki Address: 7624, Pécs, Szigeti út 12.; Tel.: 06-72-536- 288; Fax.:06-72- 536-289 Dr. Ferenc Dr. Péter www.immbio.hu Boldizsár Engelmann Introducing the subject 3. -
And Function in Aged Spleens Attrition of T Cell Zone Fibroblastic
Attrition of T Cell Zone Fibroblastic Reticular Cell Number and Function in Aged Spleens April R. Masters, Evan R. Jellison, Lynn Puddington, Kamal M. Khanna and Laura Haynes Downloaded from ImmunoHorizons 2018, 2 (5) 155-163 doi: https://doi.org/10.4049/immunohorizons.1700062 http://www.immunohorizons.org/content/2/5/155 This information is current as of September 24, 2021. http://www.immunohorizons.org/ Supplementary http://www.immunohorizons.org/content/suppl/2018/05/21/2.5.155.DCSupp Material lemental References This article cites 61 articles, 19 of which you can access for free at: http://www.immunohorizons.org/content/2/5/155.full#ref-list-1 Email Alerts Receive free email-alerts when new articles cite this article. Sign up at: by guest on September 24, 2021 http://www.immunohorizons.org/alerts ImmunoHorizons is an open access journal published by The American Association of Immunologists, Inc., 1451 Rockville Pike, Suite 650, Rockville, MD 20852 All rights reserved. ISSN 2573-7732. RESEARCH ARTICLE Adaptive Immunity Attrition of T Cell Zone Fibroblastic Reticular Cell Number and Function in Aged Spleens April R. Masters,*,† Evan R. Jellison,* Lynn Puddington,* Kamal M. Khanna,*,‡ and Laura Haynes*,† *Department of Immunology, UConn Health, Farmington, CT 06030; †Center on Aging, UConn Health, Farmington, CT 06030; and ‡Department of Microbiology, New York University, New York, NY 10003 Downloaded from ABSTRACT Aging has a profound impact on multiple facets of the immune system, culminating in aberrant functionality. The architectural disorganization http://www.immunohorizons.org/ of splenic white pulp is a hallmark of the aging spleen, yet the factors underlying these structural changes are unclear. -
B-Chapter 2.P65
1 2 3 4 CHAPTER 2 / MICROANATOMY OF MAMMALIAN SPLEEN 11 5 6 7 8 9 10 11 2 The Microanatomy 12 13 of the Mammalian Spleen 14 15 Mechanisms of Splenic Clearance 16 17 18 19 FERN TABLIN, VMD, PhD, JACK K. CHAMBERLAIN, MD, FACP, 20 AND LEON WEISS, MD 21 22 23 2.1. INTRODUCTION 2.2.1. CAPSULE AND TRABECULAE The human spleen 24 weighs approx 150 g, in adults, and is enclosed by a capsule com- The spleen is a uniquely adapted lymphoid organ that is dedi- 25 posed of dense connective tissue, with little smooth muscle (Faller, cated to the clearance of blood cells, microorganisms, and other 26 1985; Weiss, 1983, 1985). This arrangement reflects the minimal particles from the blood. This chapter deals with the microanatomy 27 contractile role of the capsule and trabeculae in altering the blood of the spleen, its highly specialized extracellular matrix compo- volume of the human spleen, under normal circumstances. The 28 nents, distinctive vascular endothelial cell receptors, and the extra- capsule measures 1.1–1.5 mm thick, and is covered by a serosa, 29 ordinary organization of the venous vasculature. We also address except at the hilus, where blood vessels, nerves, and lymphatics 30 the cellular mechanisms of splenic clearance, which are typified by enter the organ. There are two layers of the capsule: This can be 31 the vascular organization of the spleen; mechanisms and regula- determined by the orientation of collagen fibers (Faller, 1985), 32 tion of clearance, and the development of a unique component; which are moderately thick and uniform, but which become finer 33 specialized barrier cells, which may be essential to the spleen’s in the deeper regions, where the transition to pulp fibers occurs. -