Connective Tissue Histology Lecture Series
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Basic Histology and Connective Tissue Chapter 5
Basic Histology and Connective Tissue Chapter 5 • Histology, the Study of Tissues • Tissue Types • Connective Tissues Histology is the Study of Tissues • 200 different types of cells in the human body. • A Tissue consist of two or more types of cells that function together. • Four basic types of tissues: – epithelial tissue – connective tissue – muscular tissue – nervous tissue • An Organ is a structure with discrete boundaries that is composed of 2 or more tissue types. • Example: skin is an organ composed of epidermal tissue and dermal tissue. Distinguishing Features of Tissue Types • Types of cells (shapes and functions) • Arrangement of cells • Characteristics of the Extracellular Matrix: – proportion of water – types of fibrous proteins – composition of the ground substance • ground substance is the gelatinous material between cells in addition to the water and fibrous proteins • ground substance consistency may be liquid (plasma), rubbery (cartilage), stony (bone), elastic (tendon) • Amount of space occupied by cells versus extracellular matrix distinguishes connective tissue from other tissues – cells of connective tissues are widely separated by a large amount of extracellular matrix – very little extracellular matrix between the cells of epithelia, nerve, and muscle tissue Embryonic Tissues • An embryo begins as a single cell that divides into many cells that eventually forms 3 Primary Layers: – ectoderm (outer layer) • forms epidermis and nervous system – endoderm (inner layer) • forms digestive glands and the mucous membrane lining digestive tract and respiratory system – mesoderm (middle layer) • Forms muscle, bone, blood and other organs. Histotechnology • Preparation of specimens for histology: – preserve tissue in a fixative to prevent decay (formalin) – dehydrate in solvents like alcohol and xylene – embed in wax or plastic – slice into very thin sections only 1 or 2 cells thick – float slices on water and mount on slides and then add color with stains • Sectioning an organ or tissue reduces a 3-dimensional structure to a 2- dimensional slice. -
Diverse Repertoire of Human Adipocyte Subtypes Develops from Transcriptionally Distinct Mesenchymal Progenitor Cells
Diverse repertoire of human adipocyte subtypes develops from transcriptionally distinct mesenchymal progenitor cells So Yun Mina,b, Anand Desaia, Zinger Yanga,b, Agastya Sharmaa, Tiffany DeSouzaa, Ryan M. J. Gengaa,b,c, Alper Kucukurald, Lawrence M. Lifshitza, Søren Nielsene,f, Camilla Scheelee,f,g, René Maehra,c, Manuel Garbera,d, and Silvia Corveraa,1 aProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655; bGraduate School of Biomedical Sciences, University of Massachusetts Medical School, Worcester, MA 01655; cDepartment of Medicine, Diabetes Center of Excellence, University of Massachusetts Medical School, Worcester, MA 01655; dProgram in Bioinformatics, University of Massachusetts Medical School, Worcester, MA 01655; eCentre of Inflammation and Metabolism, Rigshospitalet, University of Copenhagen, 1165 Copenhagen Denmark; fCentre for Physical Activity Research, Rigshospitalet, University of Copenhagen, 1165 Copenhagen Denmark; and gNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Science, University of Copenhagen, 1165 Copenhagen, Denmark Edited by Rana K. Gupta, University of Texas Southwestern Medical Center, Dallas, TX, and accepted by Editorial Board Member David J. Mangelsdorf July12, 2019 (received for review April 16, 2019) Single-cell sequencing technologies have revealed an unexpectedly UCP1 in response to stimulation. Lineage-tracing and gene- broad repertoire of cells required to mediate complex functions in expression studies point to distinct developmental origins for multicellular organisms. Despite the multiple roles of adipose tissue these adipocyte subtypes (5, 6). In adult humans, no specific depot + in maintaining systemic metabolic homeostasis, adipocytes are is solely composed of UCP1-containing adipocytes, but UCP-1 thought to be largely homogenous with only 2 major subtypes cells can be found interspersed within supraclavicular, para- recognized in humans so far. -
Connective Tissue • Includes Things Like Bone, Fat, & Blood. All
Connective Tissue • includes things like bone, fat, & blood. All connective tissues include: 1. specialized cells 2.extracellular protein fibers } matrix that surrounds cells. 3. a fluid known as ground substance Functions include: Connective tissues come in 3 major types •Establish a structural framework 1. Connective tissue proper •Transporting fluids from one part of the body to another 2. Fluid Connective Tissue •Protecting delicate organs •Supporting, surrounding and interconnecting 3. Supporting Connective Tissue other tissue types • Other CTP cells are involved in defense and Connective Tissue Proper large repair jobs (these roam from site to site as • Connective tissue with many cell types and needed) extracellular fibers in a syrupy ground substance. A. Macrophages • Some cells of CTP are involved w/repair, B. Mast cells maintenance, and energy storage. C. Lymphocytes a. Fibroblasts D. plasma cells E. Microphages b. Adipocytes • The number of cells and cell types within a tissue at c. Mesenchymal cells any given moment varies depending on local conditions. 1 The Cell Population C. Adipocytes A. Fibroblasts • Fat cells • Most abundant cells in CTP • Typically contain a single enormous lipid droplet • Permanent resident of CTP (always present) • Other organelles squeezed to side of cell wall • Produce proteins to make the ground substance (resemble a class ring) very viscous • Also secret e prot ei ns th at mak e th e fib ers DMD. Mesenc hyma l ce lls • Stem cells B. Macrophages • Large amoeboid cells • Respond to injury by dividing into daughter cells which differentiate into connective tissue cells • Engulf & digest pathogens or damaged cells that enter the tissue • Release chemicals that activate the bodies immune system E. -
Connective Tissue N. Swailes, Ph.D. Department of Anatomy and Cell
Module 1.3: Connective Tissue 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, 13th Edition, Chapter 5 (also via AccessMedicine) Learning objectives 1) Name the three major classes of connective tissue and give examples of each. 2) Identify and describe the origin, organization and fate of embryonic connective tissue 3) Identify and discuss the functional properties imparted to tissue by the extracellular matrix: a. fibers (elastin, collagen Type I, II, III, IV and VII) b. ground substance (glycosaminoglycans, proteoglycans, glycoproteins) 4) Distinguish between different connective tissue cells and discuss their roles: a. fibroblasts b. adipocytes c. macrophages d. mast cells e. lymphocytes f. plasma cells g. eosinophils h. neutrophils 5) Classify the different connective tissues proper and compare and contrast their functional roles within an organ. Introduction The human body is made up of only four basic tissues: 1. Epithelial tissue 2. Connective tissue 3. Muscle tissue 4. Nervous tissue By adjusting the organization, composition and special features associated with each of these tissues is is possible to impart a wide variety of functions to the region or organ that they form. During this lecture you will examine the basic histological structure and function of Connective Tissue. 1 | Page: Connective Tissue Swailes a loose meshwork Part A: General characteristics of connective tissues that cushions and allows diffusion A1. There are three major classes of connective tissue i. Connective tissues proper - the most common class of connective tissue in the body. -
Reactive Stroma in Human Prostate Cancer: Induction of Myofibroblast Phenotype and Extracellular Matrix Remodeling1
2912 Vol. 8, 2912–2923, September 2002 Clinical Cancer Research Reactive Stroma in Human Prostate Cancer: Induction of Myofibroblast Phenotype and Extracellular Matrix Remodeling1 Jennifer A. Tuxhorn, Gustavo E. Ayala, Conclusions: The stromal microenvironment in human Megan J. Smith, Vincent C. Smith, prostate cancer is altered compared with normal stroma and Truong D. Dang, and David R. Rowley2 exhibits features of a wound repair stroma. Reactive stroma is composed of myofibroblasts and fibroblasts stimulated to Departments of Molecular and Cellular Biology [J. A. T., T. D. D., express extracellular matrix components. Reactive stroma D. R. R.] and Pathology [G. E. A., M. J. S., V. C. S.] Baylor College of Medicine, Houston, Texas 77030 appears to be initiated during PIN and evolve with cancer progression to effectively displace the normal fibromuscular stroma. These studies and others suggest that TGF-1isa ABSTRACT candidate regulator of reactive stroma during prostate can- Purpose: Generation of a reactive stroma environment cer progression. occurs in many human cancers and is likely to promote tumorigenesis. However, reactive stroma in human prostate INTRODUCTION cancer has not been defined. We examined stromal cell Activation of the host stromal microenvironment is pre- phenotype and expression of extracellular matrix compo- dicted to be a critical step in adenocarcinoma growth and nents in an effort to define the reactive stroma environ- progression (1–5). Several human cancers have been shown to ment and to determine its ontogeny during prostate cancer induce a stromal reaction or desmoplasia as a component of progression. carcinoma progression. However, the specific mechanisms of Experimental Design: Normal prostate, prostatic intra- stromal cell activation are not known, and the extent to which epithelial neoplasia (PIN), and prostate cancer were exam- stroma regulates the biology of tumorigenesis is not fully un- ined by immunohistochemistry. -
Endotrophin Triggers Adipose Tissue Fibrosis and Metabolic Dysfunction
ARTICLE Received 12 Sep 2013 | Accepted 21 Feb 2014 | Published 19 Mar 2014 DOI: 10.1038/ncomms4485 Endotrophin triggers adipose tissue fibrosis and metabolic dysfunction Kai Sun1,*, Jiyoung Park1,2,*, Olga T. Gupta1, William L. Holland1, Pernille Auerbach3, Ningyan Zhang4, Roberta Goncalves Marangoni5, Sarah M. Nicoloro6, Michael P. Czech6, John Varga5, Thorkil Ploug3, Zhiqiang An4 & Philipp E. Scherer1,7 We recently identified endotrophin as an adipokine with potent tumour-promoting effects. However, the direct effects of local accumulation of endotrophin in adipose tissue have not yet been studied. Here we use a doxycycline-inducible adipocyte-specific endotrophin overexpression model to demonstrate that endotrophin plays a pivotal role in shaping a metabolically unfavourable microenvironment in adipose tissue during consumption of a high-fat diet (HFD). Endotrophin serves as a powerful co-stimulator of pathologically relevant pathways within the ‘unhealthy’ adipose tissue milieu, triggering fibrosis and inflammation and ultimately leading to enhanced insulin resistance. We further demonstrate that blocking endotrophin with a neutralizing antibody ameliorates metabolically adverse effects and effectively reverses metabolic dysfunction induced during HFD exposure. Collectively, our findings demonstrate that endotrophin exerts a major influence in adipose tissue, eventually resulting in systemic elevation of pro-inflammatory cytokines and insulin resistance, and the results establish endotrophin as a potential target in the context of metabolism and cancer. 1 Touchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA. 2 Department of Biological Sciences, School of Life Sciences, Ulsan National Institute of Science and Technology, 50 UNIST street, Ulsan 689-798, Korea. -
Pg 131 Chondroblast -> Chondrocyte (Lacunae) Firm Ground Substance
Figure 4.8g Connective tissues. Chondroblast ‐> Chondrocyte (Lacunae) Firm ground substance (chondroitin sulfate and water) Collagenous and elastic fibers (g) Cartilage: hyaline No BV or nerves Description: Amorphous but firm Perichondrium (dense irregular) matrix; collagen fibers form an imperceptible network; chondroblasts produce the matrix and when mature (chondrocytes) lie in lacunae. Function: Supports and reinforces; has resilient cushioning properties; resists compressive stress. Location: Forms most of the embryonic skeleton; covers the ends Chondrocyte of long bones in joint cavities; forms in lacuna costal cartilages of the ribs; cartilages of the nose, trachea, and larynx. Matrix Costal Photomicrograph: Hyaline cartilage from the cartilages trachea (750x). Thickness? Metabolism? Copyright © 2010 Pearson Education, Inc. Pg 131 Figure 6.1 The bones and cartilages of the human skeleton. Epiglottis Support Thyroid Larynx Smooth Cartilage in Cartilages in cartilage external ear nose surface Cricoid Trachea Articular Lung Cushions cartilage Cartilage of a joint Cartilage in Costal Intervertebral cartilage disc Respiratory tube cartilages in neck and thorax Pubic Bones of skeleton symphysis Meniscus (padlike Axial skeleton cartilage in Appendicular skeleton knee joint) Cartilages Articular cartilage of a joint Hyaline cartilages Elastic cartilages Fibrocartilages Pg 174 Copyright © 2010 Pearson Education, Inc. Figure 4.8g Connective tissues. (g) Cartilage: hyaline Description: Amorphous but firm matrix; collagen fibers form an imperceptible network; chondroblasts produce the matrix and when mature (chondrocytes) lie in lacunae. Function: Supports and reinforces; has resilient cushioning properties; resists compressive stress. Location: Forms most of the embryonic skeleton; covers the ends Chondrocyte of long bones in joint cavities; forms in lacuna costal cartilages of the ribs; cartilages of the nose, trachea, and larynx. -
Profiling Microdissected Epithelium and Stroma to Model Genomic Signatures for Cervical Carcinogenesis Accommodating for Covariates
Research Article Profiling Microdissected Epithelium and Stroma to Model Genomic Signatures for Cervical Carcinogenesis Accommodating for Covariates David Gius,1 Margo C. Funk,2 Eric Y. Chuang,1 Sheng Feng,3 Phyllis C. Huettner,4 Loan Nguyen,2 C. Matthew Bradbury,1 Mark Mishra,1 Shuping Gao,1 Barbara M. Buttin,2 David E. Cohn,2 Matthew A. Powell,2 Neil S. Horowitz,2 Bradford P. Whitcomb,2 and JanetS. Rader 2 1Radiation Oncology Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland and 2Division of Gynecologic Oncology, Department of Obstetrics and Gynecology; 3Division of Biostatistics; and 4Lauren V. Ackerman Laboratory of Surgical Pathology, Washington University School of Medicine, St. Louis, Missouri Abstract (CIN 1–3) and finally to squamous cell carcinoma antigen (SCCA) This study is the first comprehensive, integrated approach to have been well characterized. Histologically, CIN 1 consists of examine grade-specific changes in gene expression along the immature basal-type cells involving the lower third of the entire neoplastic spectrum of cervical intraepithelial neoplasia epithelium. In CIN 2, these immature basal-type cells involve more (CIN) in the process of cervical carcinogenesis. This was than the lower third, whereas CIN 3 involves the full thickness of the accomplished by identifying gene expression signatures of epithelium. In addition, higher CIN grades exhibit nuclear crowding, disease progression using cDNA microarrays to analyze RNA pleomorphism, loss of cell polarity, and increased mitotic activity from laser-captured microdissected epithelium and underlying (1). These transitions seemto be well conserved and, as such, stroma from normal cervix, graded CINs, cancer, and patient- provide an intriguing systemto use genomicsto identify the early matched normal cervical tissues. -
Normal Gross and Histologic Features of the Gastrointestinal Tract
NORMAL GROSS AND HISTOLOGIC 1 FEATURES OF THE GASTROINTESTINAL TRACT THE NORMAL ESOPHAGUS left gastric, left phrenic, and left hepatic accessory arteries. Veins in the proximal and mid esopha- Anatomy gus drain into the systemic circulation, whereas Gross Anatomy. The adult esophagus is a the short gastric and left gastric veins of the muscular tube measuring approximately 25 cm portal system drain the distal esophagus. Linear and extending from the lower border of the cri- arrays of large caliber veins are unique to the distal coid cartilage to the gastroesophageal junction. esophagus and can be a helpful clue to the site of It lies posterior to the trachea and left atrium a biopsy when extensive cardiac-type mucosa is in the mediastinum but deviates slightly to the present near the gastroesophageal junction (4). left before descending to the diaphragm, where Lymphatic vessels are present in all layers of the it traverses the hiatus and enters the abdomen. esophagus. They drain to paratracheal and deep The subdiaphragmatic esophagus lies against cervical lymph nodes in the cervical esophagus, the posterior surface of the left hepatic lobe (1). bronchial and posterior mediastinal lymph nodes The International Classification of Diseases in the thoracic esophagus, and left gastric lymph and the American Joint Commission on Cancer nodes in the abdominal esophagus. divide the esophagus into upper, middle, and lower thirds, whereas endoscopists measure distance to points in the esophagus relative to the incisors (2). The esophagus begins 15 cm from the incisors and extends 40 cm from the incisors in the average adult (3). The upper and lower esophageal sphincters represent areas of increased resting tone but lack anatomic landmarks; they are located 15 to 18 cm from the incisors and slightly proximal to the gastroesophageal junction, respectively. -
The Plantar Aponeurosis in Fetuses and Adults: an Aponeurosis Or Fascia?
Int. J. Morphol., 35(2):684-690, 2017. The Plantar Aponeurosis in Fetuses and Adults: An Aponeurosis or Fascia? La Aponeurosis Plantar en Fetos y Adultos: ¿Aponeurosis o Fascia? A. Kalicharan; P. Pillay; C.O. Rennie; B.Z. De Gama & K.S. Satyapal KALICHARAN, A.; PILLAY, P.; RENNIE, C.O.; DE GAMA, B. Z. & SATYAPAL, K. S. The plantar aponeurosis in fetuses and adults: An aponeurosis or fascia? Int. J. Morphol., 35(2):684-690, 2017. SUMMARY: The plantar aponeurosis (PA), which is a thickened layer of deep fascia located on the plantar surface of the foot, is comprised of three parts. There are differing opinions on its nomenclature since various authors use the terms PA and plantar fascia (PF) interchangeably. In addition, the variable classifications of its parts has led to confusion. In order to assess the nature of the PA, this study documented its morphology. Furthermore, a pilot histological analysis was conducted to examine whether the structure is an aponeurosis or fascia. This study comprised of a morphological analysis of the three parts of the PA by micro- and macro-dissection of 50 fetal and 50 adult cadaveric feet, respectively (total n=100). Furthermore, a pilot histological analysis was conducted on five fetuses (n=10) and five adults (n=10) (total n=20). In each foot, the histological analysis was conducted on the three parts of the plantar aponeurosis, i.e. the central, lateral, and medial at their calcaneal origin (total n=60). Fetuses: i) Morphology: In 66 % (33/50) of the specimens, the standard anatomical pattern was observed, viz. -
Pressure Ulcer Staging Guide
Pressure Ulcer Staging Guide Pressure Ulcer Staging Guide STAGE I STAGE IV Intact skin with non-blanchable Full thickness tissue loss with exposed redness of a localized area usually Reddened area bone, tendon, or muscle. Slough or eschar may be present on some parts Epidermis over a bony prominence. Darkly Epidermis pigmented skin may not have of the wound bed. Often includes undermining and tunneling. The depth visible blanching; its color may Dermis of a stage IV pressure ulcer varies by Dermis differ from the surrounding area. anatomical location. The bridge of the This area may be painful, firm, soft, nose, ear, occiput, and malleolus do not warmer, or cooler as compared to have subcutaneous tissue and these adjacent tissue. Stage I may be Adipose tissue ulcers can be shallow. Stage IV ulcers Adipose tissue difficult to detect in individuals with can extend into muscle and/or Muscle dark skin tones. May indicate "at supporting structures (e.g., fascia, Muscle risk" persons (a heralding sign of Bone tendon, or joint capsule) making risk). osteomyelitis possible. Exposed bone/ Bone tendon is visible or directly palpable. STAGE II DEEP TISSUE INJURY Partial thickness loss of dermis Blister Purple or maroon localized area of Reddened area presenting as a shallow open ulcer discolored intact skin or blood-filled Epidermis with a red pink wound bed, without Epidermis blister due to damage of underlying soft slough. May also present as an tissue from pressure and/or shear. The intact or open/ruptured serum-filled Dermis area may be preceded by tissue that is Dermis blister. -
Altered Adipose Tissue and Adipocyte Function in the Pathogenesis of Metabolic Syndrome
Altered adipose tissue and adipocyte function in the pathogenesis of metabolic syndrome C. Ronald Kahn, … , Guoxiao Wang, Kevin Y. Lee J Clin Invest. 2019;129(10):3990-4000. https://doi.org/10.1172/JCI129187. Review Series Over the past decade, great progress has been made in understanding the complexity of adipose tissue biology and its role in metabolism. This includes new insights into the multiple layers of adipose tissue heterogeneity, not only differences between white and brown adipocytes, but also differences in white adipose tissue at the depot level and even heterogeneity of white adipocytes within a single depot. These inter- and intra-depot differences in adipocytes are developmentally programmed and contribute to the wide range of effects observed in disorders with fat excess (overweight/obesity) or fat loss (lipodystrophy). Recent studies also highlight the underappreciated dynamic nature of adipose tissue, including potential to undergo rapid turnover and dedifferentiation and as a source of stem cells. Finally, we explore the rapidly expanding field of adipose tissue as an endocrine organ, and how adipose tissue communicates with other tissues to regulate systemic metabolism both centrally and peripherally through secretion of adipocyte-derived peptide hormones, inflammatory mediators, signaling lipids, and miRNAs packaged in exosomes. Together these attributes and complexities create a robust, multidimensional signaling network that is central to metabolic homeostasis. Find the latest version: https://jci.me/129187/pdf REVIEW SERIES: MECHANISMS UNDERLYING THE METABOLIC SYNDROME The Journal of Clinical Investigation Series Editor: Philipp E. Scherer Altered adipose tissue and adipocyte function in the pathogenesis of metabolic syndrome C. Ronald Kahn,1 Guoxiao Wang,1 and Kevin Y.