Anatomy and Histology of the Pancreas (Version 2.0)
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Te2, Part Iii
TERMINOLOGIA EMBRYOLOGICA Second Edition International Embryological Terminology FIPAT The Federative International Programme for Anatomical Terminology A programme of the International Federation of Associations of Anatomists (IFAA) TE2, PART III Contents Caput V: Organogenesis Chapter 5: Organogenesis (continued) Systema respiratorium Respiratory system Systema urinarium Urinary system Systemata genitalia Genital systems Coeloma Coelom Glandulae endocrinae Endocrine glands Systema cardiovasculare Cardiovascular system Systema lymphoideum Lymphoid system Bibliographic Reference Citation: FIPAT. Terminologia Embryologica. 2nd ed. FIPAT.library.dal.ca. Federative International Programme for Anatomical Terminology, February 2017 Published pending approval by the General Assembly at the next Congress of IFAA (2019) Creative Commons License: The publication of Terminologia Embryologica is under a Creative Commons Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0) license The individual terms in this terminology are within the public domain. Statements about terms being part of this international standard terminology should use the above bibliographic reference to cite this terminology. The unaltered PDF files of this terminology may be freely copied and distributed by users. IFAA member societies are authorized to publish translations of this terminology. Authors of other works that might be considered derivative should write to the Chair of FIPAT for permission to publish a derivative work. Caput V: ORGANOGENESIS Chapter 5: ORGANOGENESIS -
Pancreatic B-Cell Replacement: Advances in Protocols Used for Differentiation of Pancreatic Progenitors to B-Like Cells
FOLIA HISTOCHEMICA REVIEW ET CYTOBIOLOGICA Vol. 57, No. 3, 2019 pp. 101–115 Pancreatic b-cell replacement: advances in protocols used for differentiation of pancreatic progenitors to b-like cells Muhammad Waseem Ghani1, Li Ye1, Zhao Yi1, Hammad Ghani2, Muhammad Waseem Birmani1, Aamir Nawab1, Lang Guan Cun1, Liu Bin1, Xiao Mei1 1Department of Livestock Production and Management, Agricultural College, Guangdong Ocean University, Zhanjiang, Guangdong, China 2Nawaz Sharif Medical College University of Gujrat, Punjab, Pakistan Abstract Insulin-producing cells derived from in vitro differentiation of stem cells and non-stem cells by using different factors can spare the need for genetic manipulation and provide a cure for diabetes. In this context, pancreatic progenitors differentiating to b-like cells garner increasing attention as b-cell replacement source. This kind of cell therapy has the potential to cure diabetes, but is still on its way of being clinically useful. The primary restriction for in vitro production of mature and functional b-cells is developing a physiologically relevant in vitro culture system which can mimic in vivo pathways of islet development. In order to achieve this target, different approaches have been attempted for the differentiation of pancreatic stem/progenitor cells to b-like cells. Here, we will review some of the state-of-the-art protocols for the differentiation of pancreatic progenitors and differentiated pancreatic cells into b-like cells with a focus on pancreatic duct cells. (Folia Histochemica et Cytobiologica -
Vocabulario De Morfoloxía, Anatomía E Citoloxía Veterinaria
Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) Servizo de Normalización Lingüística Universidade de Santiago de Compostela COLECCIÓN VOCABULARIOS TEMÁTICOS N.º 4 SERVIZO DE NORMALIZACIÓN LINGÜÍSTICA Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) 2008 UNIVERSIDADE DE SANTIAGO DE COMPOSTELA VOCABULARIO de morfoloxía, anatomía e citoloxía veterinaria : (galego-español- inglés) / coordinador Xusto A. Rodríguez Río, Servizo de Normalización Lingüística ; autores Matilde Lombardero Fernández ... [et al.]. – Santiago de Compostela : Universidade de Santiago de Compostela, Servizo de Publicacións e Intercambio Científico, 2008. – 369 p. ; 21 cm. – (Vocabularios temáticos ; 4). - D.L. C 2458-2008. – ISBN 978-84-9887-018-3 1.Medicina �������������������������������������������������������������������������veterinaria-Diccionarios�������������������������������������������������. 2.Galego (Lingua)-Glosarios, vocabularios, etc. políglotas. I.Lombardero Fernández, Matilde. II.Rodríguez Rio, Xusto A. coord. III. Universidade de Santiago de Compostela. Servizo de Normalización Lingüística, coord. IV.Universidade de Santiago de Compostela. Servizo de Publicacións e Intercambio Científico, ed. V.Serie. 591.4(038)=699=60=20 Coordinador Xusto A. Rodríguez Río (Área de Terminoloxía. Servizo de Normalización Lingüística. Universidade de Santiago de Compostela) Autoras/res Matilde Lombardero Fernández (doutora en Veterinaria e profesora do Departamento de Anatomía e Produción Animal. -
Primary Outgrowth Cultures Are a Reliable Source of Human Pancreatic
Laboratory Investigation (2015) 95, 1331–1340 © 2015 USCAP, Inc All rights reserved 0023-6837/15 Primary outgrowth cultures are a reliable source of human pancreatic stellate cells Song Han1,4, Daniel Delitto1,4, Dongyu Zhang1, Heather L Sorenson2, George A Sarosi1,3, Ryan M Thomas1,3, Kevin E Behrns1, Shannon M Wallet2, Jose G Trevino1 and Steven J Hughes1 Recent advances demonstrate a critical yet poorly understood role for the pancreatic stellate cell (PSC) in the pathogenesis of chronic pancreatitis (CP) and pancreatic cancer (PC). Progress in this area has been hampered by the availability, fidelity, and/or reliability of in vitro models of PSCs. We examined whether outgrowth cultures from human surgical specimens exhibited reproducible phenotypic and functional characteristics of PSCs. PSCs were cultured from surgical specimens of healthy pancreas, CP and PC. Growth dynamics, phenotypic characteristics, soluble mediator secretion profiles and co-culture with PC cells both in vitro and in vivo were assessed. Forty-seven primary cultures were established from 52 attempts, demonstrating universal α-smooth muscle actin and glial fibrillary acidic protein but negligible epithelial surface antigen expression. Modification of culture conditions consistently led to cytoplasmic lipid accumulation, suggesting induction of a quiescent phenotype. Secretion of growth factors, chemokines and cytokines did not significantly differ between donor pathologies, but did evolve over time in culture. Co-culture of PSCs with established PC cell lines resulted in significant changes in levels of multiple secreted mediators. Primary PSCs co-inoculated with PC cells in a xenograft model led to augmented tumor growth and metastasis. Therefore, regardless of donor pathology, outgrowth cultures produce PSCs that demonstrate consistent growth and protein secretion properties. -
Epithelium 2 : Glandular Epithelium Histology Laboratory -‐ Year 1, Fall Term Dr
Epithelium 2 : Glandular Epithelium Histology Laboratory -‐ Year 1, Fall Term Dr. Heather Yule ([email protected]) October 21, 2014 Slides for study: 75 (Salivary Gland), 355 (Pancreas Tail), 48 (Atrophic Mammary Gland), 49 (Active Mammary Gland) and 50 (Resting Mammary Gland) Electron micrographs for : study EM: Serous acinus in parotid gland EM: Mucous acinus in mixed salivary gland EM: Pancreatic acinar cell Main Objective: Understand key histological features of glandular epithelium and relate structure to function. Specific Objectives: 1. Describe key histological differences between endocrine and exocrine glands including their development. 2. Compare three modes of secretion in glands; holocrine, apocrine and merocrine. 3. Explain the functional significance of polarization of glandular epithelial cells. 4. Define the terms parenchyma, stroma, mucous acinus, serous acinus and serous a demilune and be able to them identify in glandular tissue. 5. Distinguish exocrine and endocrine pancreas. 6. Compare the histology of resting, lactating and postmenopausal mammary glands. Keywords: endocrine gland, exocrine gland, holocrine, apocrine, merocrine, polarity, parenchyma, stroma, acinus, myoepithelial cell, mucous gland, serous gland, mixed or seromucous gland, serous demilune, exocrine pancreas, endocrine pancreas (pancreatic islets), resting mammary gland, lactating mammary gland, postmenopausal mammary gland “This copy is made solely for your personal use for research, private study, education, parody, satire, criticism, or review -
An Analysis of Benign Human Prostate Offers Insights Into the Mechanism
www.nature.com/scientificreports OPEN An analysis of benign human prostate ofers insights into the mechanism of apocrine secretion Received: 12 March 2018 Accepted: 22 February 2019 and the origin of prostasomes Published: xx xx xxxx Nigel J. Fullwood 1, Alan J. Lawlor2, Pierre L. Martin-Hirsch3, Shyam S. Matanhelia3 & Francis L. Martin 4 The structure and function of normal human prostate is still not fully understood. Herein, we concentrate on the diferent cell types present in normal prostate, describing some previously unreported types and provide evidence that prostasomes are primarily produced by apocrine secretion. Patients (n = 10) undergoing TURP were prospectively consented based on their having a low risk of harbouring CaP. Scanning electron microscopy and transmission electron microscopy was used to characterise cell types and modes of secretion. Zinc levels were determined using Inductively Coupled Plasma Mass Spectrometry. Although merocrine secretory cells were noted, the majority of secretory cells appear to be apocrine; for the frst time, we clearly show high-resolution images of the stages of aposome secretion in human prostate. We also report a previously undescribed type of epithelial cell and the frst ultrastructural image of wrapping cells in human prostate stroma. The zinc levels in the tissues examined were uniformly high and X-ray microanalysis detected zinc in merocrine cells but not in prostasomes. We conclude that a signifcant proportion of prostasomes, possibly the majority, are generated via apocrine secretion. This fnding provides an explanation as to why so many large proteins, without a signal peptide sequence, are present in the prostatic fuid. Tere are many complications associated with the prostate from middle age onwards, including benign prostatic hyperplasia (BPH) and prostate cancer (PCa). -
Epithelium and Glands
EPITHELIUM AND GLANDS OBJECTIVES: After completing this exercise, students should be able to do the following: 1. Identify glands. 2. Classify glands based on secretory type. ASSIGNMENT FOR TODAY'S LABORATORY GLASS SLIDES SL 111 (Trachea) cilia and unicellular glands (goblet cells) SL 019 (Jejunum, PAS) unicellular glands SL 092 (Submandibular gland) serous, mucous and demilune secretory units SL 093 (Sublingual gland) mucous secretory units POSTED ELECTRON MICROGRAPHS # 7 Organelles # 11 Desmosomes # 12 Epithelium # 13 Freeze-fracture Lab 5 Posted EMs; Lab 5 Posted EMs with some yellow labels SUPPLEMENTAL MATERIAL: SUPPLEMENTARY ELECTRON MICROGRAPHS Rhodin, J. A.G., An Atlas of Histology. Glands pp. 46 - 52 Copies of this text are on reserve in the HSL. Glandular epithelium is specialized for the production and secretion of products. The cells that form glands are usually cuboidal or columnar in shape. In this exercise we are emphasizing morphological differences in glands with respect to secretory products. A. UNICELLULAR GLANDS: SL 111 (low, high), (Trachea, H&E); SL 019 (oil), (Jejunum, PAS), for review. Goblet cells may be few or numerous and are found in epithelia of the respiratory and alimentary systems. The secretory product is emptied into the lumen of the organ rather than into ducts (J. Fig. 4-18, 15-24; R. 5.38, Plate 60) B. MULTICELLULAR GLANDS: In general these glands are formed by invagination, proliferation, and differentiation of the epithelium from which they are derived. Glands that maintain a connection with the surface epithelium through ducts are termed exocrine glands, whereas glands that have lost this connection, and secrete instead to blood vessels, are called endocrine glands (see J. -
Exocrine Glands Ccasslassified Da Acco Rd Ing to
Glandular tissues Danil Hammoudi.MD A gland is an organ that synthesizes a substance for relfbthlease of substances such •as hormones • breast milk, •often into the bloodstream (endocrine gland) • into cavities inside the body or its outer surface (exocrine gland). Myoepithelial Cells • These are contractile cells that lie within the basal lamina in the secretory ppgortion of glands and intercalated ducts, which form the initial portion of the duct system. • They are instrumental in moving the secretions toward the excretory duct. Histologically, glands are described using some standard vocabulary, with which you should be familiar. exocrine / endocrine Destination of product: Nature of product: serous / mucous / mixed Location of gland: mucosal / submucosal Arrangement of secretory cells: acinus / tubule / cord Number of interconnected units: simple / compound intercalated / striated Duct function: secret/tory / excre tory Duct location: intralobular / interlobular / interlobar Tissue composition: parenchyma / stroma The endocrine system of humans Pineal gland Hypothalamus Posterior pituitary Anterior pituitary Thyroid Parathyroid Thymus Heart Liver Stomach and small intestine Pancreas Adrenal cortex Adrenal medulla Kidney Skin Silverthorn, Human Gonads Physiology, 3rd edition Figure 7-2 Duussgadsapoduoosctless glands that produce hormones Secretions include amino acids, proteins, glycoproteins, and steroids Endocrine Glands More numerous than endocrine glands Secrete their products onto body surfaces (skin) or into body cavities -
Respiratory System 2015
Microscopic Anatomy 2015 The Respiratory System Introduction and Overview During a 24-hour period, more than 9000 liters of air enter the interior of the body to participate in gas exchange. This air must be warmed, cleansed, humidified and conducted to the respiratory surface. In the lung, gas traverses a very thin epithelium and connective tissue space to reach capillaries carrying oxygen-poor, carbon dioxide-laden blood from the right ventricle. The ventilatory mechanism consists of diaphragmatic, intercostal, and abdominal musculature as well as elastic tissue within the lung. This mechanism alternately pulls air into (inspiration) or drives air from (expiration) the lung. The lungs are capable of undergoing wide variations in size. In maximum inspiration, the lungs may hold up to 7 liters of air, and with forced expiration may hold as little as 1 liter. The respiratory system contains a proximal conducting portion that connects the exterior of the body with the distal respiratory portion where exchange of gases between air and blood occurs. The conducting portion, which consists of the nasal cavities, pharynx, larynx, and paired main bronchi, delivers air to structures within the lung where gas exchange takes place. Cellular specializations are readily apparent as one follows the flow of air from the nose to the respiratory surface. Although the lung’s primary function is gas exchange, studies over the past several decades have detailed a variety of important metabolic functions of the lung. The respiratory system represents a classic example of the relationship of structure to function. In the case of the lung’s alveoli, if the only pertinent information one had prior to viewing a histological slide was that blood carried oxygen and that the alveolus was the site of gas exchange, one could easily deduce that diffusion is the mechanism of gas exchange. -
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. -
Pancreatic Stellate Cells in Health and Disease
Pancreatic Stellate Cells in Health and Disease Alpha R. Mekapogu, Srinivasa P. Pothula, Romano C. Pirola, Jeremy S. Wilson, Minoti V. Apte Pancreatic Research Group, South Western Sydney Clinical School, Faculty of Medicine, The University of New South Wales, Ingham Institute for Applied Medical Research, Sydney, Australia e-mail: [email protected]. Version 1.0, November 17th, 2020 [DOI: 10.3998/panc.2020.08] Abstract the pancreas – chronic pancreatitis and pancreatic cancer. In health, the process of fibrogenesis is a Pancreatic stellate cells (PSCs) are resident cells well-regulated dynamic process which is of the pancreas, found in both the exocrine and necessary for regular turnover of extracellular endocrine parts of the gland. Over the two decades matrix (ECM) that allows remodeling and since these cells were first isolated and cultured maintenance of normal pancreatic architecture. from rodent and human pancreas, research in this However, during injury, the equilibrium between area has progressed at a rapid rate. Our production and degradation of fibrous tissue is knowledge of PSC biology in both health and disrupted leading to excessive deposition of disease has increased significantly. In health, extracellular matrix proteins resulting in fibrosis. PSCs are known to not only play a role in regulating normal extracellular matrix turnover but Pancreatic stellate cells (PSCs) are now are also thought to have progenitor cell functions considered to be the key contributors of pancreatic as well as a role in innate immunity. The critical fibrosis (5, 11, 135). These cells were first roles of PSCs in inflammatory as well as malignant observed by Watari et al. -
University of Southampton Research Repository Eprints Soton
University of Southampton Research Repository ePrints Soton Copyright © and Moral Rights for this thesis are retained by the author and/or other copyright owners. A copy can be downloaded for personal non-commercial research or study, without prior permission or charge. This thesis cannot be reproduced or quoted extensively from without first obtaining permission in writing from the copyright holder/s. The content must not be changed in any way or sold commercially in any format or medium without the formal permission of the copyright holders. When referring to this work, full bibliographic details including the author, title, awarding institution and date of the thesis must be given e.g. AUTHOR (year of submission) "Full thesis title", University of Southampton, name of the University School or Department, PhD Thesis, pagination http://eprints.soton.ac.uk University of Southampton Faculty of Medicine, Health and Biological Sciences Pancreatic Research Group An investigation into soluble growth factors of TIMP-1, IGF-1 and Insulin on Pancreatic stellate cell survival Dr Manish Patel DM Thesis February 2014 University of Southampton An investigation into soluble growth factors of TIMP-1, IGF-1 and Insulin on Pancreatic stellate cell survival Faculty of Medicine, Health and Biological Sciences During pancreatic injury, the pancreatic stellate cell(PSC) become activated to a myofibroblast-like phenotype, proliferate and are known to be the major source of matrix which characterise pancreatic fibrosis in chronic pancreatitis and pancreatic cancer. Activated PSC also express matrix degrading metalloproteinases(MMPs) and their tissue inhibitors(TIMPs). Previous work has demonstrated that during spontaneous recovery from experimental liver fibrosis after 4 weeks of carbon tetrachloride injections, there is a fall in the expression of TIMP-1, a loss of the hepatic stellate cells (HSCs) by apoptosis, and an increase in liver collagenolytic activity with the return of the liver to a near normal histology.