MODULE 1: HISTOLOGY I an Introduction to Histology; Begin Epithelial Tissue and Connective Tissue
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Microanatomy of Muscles
Microanatomy of Muscles Anatomy & Physiology Class Three Main Muscle Types Objectives: By the end of this presentation you will have the information to: 1. Describe the 3 main types of muscles. 2. Detail the functions of the muscle system. 3. Correctly label the parts of a myocyte (muscle cell) 4. Identify the levels of organization in a skeletal muscle from organ to myosin. 5. Explain how a muscle contracts utilizing the correct terminology of the sliding filament theory. 6. Contrast and compare cardiac and smooth muscle with skeletal muscle. Major Functions: Muscle System 1. Moving the skeletal system and posture. 2. Passing food through the digestive system & constriction of other internal organs. 3. Production of body heat. 4. Pumping the blood throughout the body. 5. Communication - writing and verbal Specialized Cells (Myocytes) ~ Contractile Cells Can shorten along one or more planes because of specialized cell membrane (sarcolemma) and specialized cytoskeleton. Specialized Structures found in Myocytes Sarcolemma: The cell membrane of a muscle cell Transverse tubule: a tubular invagination of the sarcolemma of skeletal or cardiac muscle fibers that surrounds myofibrils; involved in transmitting the action potential from the sarcolemma to the interior of the myofibril. Sarcoplasmic Reticulum: The special type of smooth endoplasmic Myofibrils: reticulum found in smooth and a contractile fibril of skeletal muscle, composed striated muscle fibers whose function mainly of actin and myosin is to store and release calcium ions. Multiple Nuclei (skeletal) & many mitochondria Skeletal Muscle - Microscopic Anatomy A whole skeletal muscle (such as the biceps brachii) is considered an organ of the muscular system. Each organ consists of skeletal muscle tissue, connective tissue, nerve tissue, and blood or vascular tissue. -
Back-To-Basics: the Intricacies of Muscle Contraction
Back-to- MIOTA Basics: The CONFERENCE OCTOBER 11, Intricacies 2019 CHERI RAMIREZ, MS, of Muscle OTRL Contraction OBJECTIVES: 1.Review the anatomical structure of a skeletal muscle. 2.Review and understand the process and relationship between skeletal muscle contraction with the vital components of the nervous system, endocrine system, and skeletal system. 3.Review the basic similarities and differences between skeletal muscle tissue, smooth muscle tissue, and cardiac muscle tissue. 4.Review the names, locations, origins, and insertions of the skeletal muscles found in the human body. 5.Apply the information learned to enhance clinical practice and understanding of the intricacies and complexity of the skeletal muscle system. 6.Apply the information learned to further educate clients on the importance of skeletal muscle movement, posture, and coordination in the process of rehabilitation, healing, and functional return. 1. Epithelial Four Basic Tissue Categories 2. Muscle 3. Nervous 4. Connective A. Loose Connective B. Bone C. Cartilage D. Blood Introduction There are 3 types of muscle tissue in the muscular system: . Skeletal muscle: Attached to bones of skeleton. Voluntary. Striated. Tubular shape. Cardiac muscle: Makes up most of the wall of the heart. Involuntary. Striated with intercalated discs. Branched shape. Smooth muscle: Found in walls of internal organs and walls of vascular system. Involuntary. Non-striated. Spindle shape. 4 Structure of a Skeletal Muscle Skeletal Muscles: Skeletal muscles are composed of: • Skeletal muscle tissue • Nervous tissue • Blood • Connective tissues 5 Connective Tissue Coverings Connective tissue coverings over skeletal muscles: .Fascia .Tendons .Aponeuroses 6 Fascia: Definition: Layers of dense connective tissue that separates muscle from adjacent muscles, by surrounding each muscle belly. -
Single-Cell Analysis Uncovers Fibroblast Heterogeneity
ARTICLE https://doi.org/10.1038/s41467-020-17740-1 OPEN Single-cell analysis uncovers fibroblast heterogeneity and criteria for fibroblast and mural cell identification and discrimination ✉ Lars Muhl 1,2 , Guillem Genové 1,2, Stefanos Leptidis 1,2, Jianping Liu 1,2, Liqun He3,4, Giuseppe Mocci1,2, Ying Sun4, Sonja Gustafsson1,2, Byambajav Buyandelger1,2, Indira V. Chivukula1,2, Åsa Segerstolpe1,2,5, Elisabeth Raschperger1,2, Emil M. Hansson1,2, Johan L. M. Björkegren 1,2,6, Xiao-Rong Peng7, ✉ Michael Vanlandewijck1,2,4, Urban Lendahl1,8 & Christer Betsholtz 1,2,4 1234567890():,; Many important cell types in adult vertebrates have a mesenchymal origin, including fibro- blasts and vascular mural cells. Although their biological importance is undisputed, the level of mesenchymal cell heterogeneity within and between organs, while appreciated, has not been analyzed in detail. Here, we compare single-cell transcriptional profiles of fibroblasts and vascular mural cells across four murine muscular organs: heart, skeletal muscle, intestine and bladder. We reveal gene expression signatures that demarcate fibroblasts from mural cells and provide molecular signatures for cell subtype identification. We observe striking inter- and intra-organ heterogeneity amongst the fibroblasts, primarily reflecting differences in the expression of extracellular matrix components. Fibroblast subtypes localize to discrete anatomical positions offering novel predictions about physiological function(s) and regulatory signaling circuits. Our data shed new light on the diversity of poorly defined classes of cells and provide a foundation for improved understanding of their roles in physiological and pathological processes. 1 Karolinska Institutet/AstraZeneca Integrated Cardio Metabolic Centre, Blickagången 6, SE-14157 Huddinge, Sweden. -
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. -
MUSCLE TISSUE Larry Johnson Texas A&M University
MUSCLE TISSUE Larry Johnson Texas A&M University Objectives • Histologically identify and functionally characterize each of the 3 types of muscle tissues. • Describe the organization of the sarcomere as seen in light and electron microscopy. • Identify the endomysium, perimysium, and epimysium CT sleeves in muscle. • Relate the functional differences of the three muscle cell types. From: Douglas P. Dohrman and TAMHSC Faculty 2012 Structure and Function of Human Organ Systems, Histology Laboratory Manual MUSCLE FUNCTION: • GENERATION OF CONTRACTILE FORCE DISTINGUISHING FEATURES: • HIGH CONCENTRATION OF CONTRACTILE PROTEINS ACTIN AND MYOSIN ARRANGED EITHER DIFFUSELY IN THE CYTOPLASM (SMOOTH MUSCLE) OR IN REGULAR REPEATING UNITS CALLED SARCOMERES (STRIATED MUSCLES, e.g., CARDIAC AND SKELETAL MUSCLES) MUSCLE • DISTRIBUTION: SKELETAL – STRIATED MUSCLES MOSTLY ASSOCIATED WITH THE SKELETON MUSCLE • DISTRIBUTION: SKELETAL – STRIATED MUSCLES MOSTLY ASSOCIATED WITH THE SKELETON CARDIAC – STRIATED MUSCLES ASSOCIATEWD WITH THE HEART MUSCLE • DISTRIBUTION: SKELETAL – STRIATED MUSCLES MOSTLY ASSOCIATED WITH THE SKELETON CARDIAC – STRIATED MUSCLES ASSOCIATEWD WITH THE HEART SMOOTH – FUSIFORM CELLS ASSOCIATED WITH THE VISCERA, RESPIRATORY TRACT, BLOOD VESSELS, UTERUS, ETC. MUSCLE • HISTOLOGICAL INDENTIFICATION: SKELETAL MUSCLE – VERY LONG CYLINDRICAL STRIATED MUSCLE CELLS WITH MULTIPLE PERIPHERAL NUCLEI MUSCLE • HISTOLOGICAL INDENTIFICATION: SKELETAL MUSCLE – VERY LONG CYLINDRICAL STRIATED MUSCLE CELLS WITH MULTIPLE PERIPHERAL NUCLEI CARDIAC MUSCLE – -
8 Skeletal M Uscle
8 Skeletal m uscle (a) Diagram of a cross section through a (c) Skeletal muscle (LS) muscle fibre: three layers of connective tissue Cross-wise striations Endomysium 20µm Epimysium Perimysium Myofibrils run longitudinally along the Capillary Endomysium muscle fiber Muscle fiber The cross striations are due to the regular repeating units along the muscle Peripheral fiber called ‘muscle sarcomeres’ nucleus (b) Skeletal muscle fibers are formed by fusion (d) Skeletal Muscle (TS) of many myoblasts Myoblasts Myoblasts Peripheral align nucleus and adhere Fusion into Perimysium Myofibrils multinucleated in cross- myotube section Differentiate Innervation Blood into mature by motor Muscle fiber vessel muscle fiber neuron 20µm Endomysium Attach Attach to tendon to tendon (e) Electron micrograph of a sarcomere (f) A sarcomere and some of its components ZZM Costamere Binding to proteins in Costamere Z-disc extracellular matrix (e.g. laminin) in Focal adhesion m T- the basal lamina T- µ SR Myofibril complex 1 tubule tubule T-tubule Sarcolemma Proteins that link focal adhesion complex to I-band A-band I-band Z-lines in the muscle sarcomere for lateral transmission of force Sarcoplasmic reticulum Z Thick filament Z Thin filament (simplified) Thick Thin The muscle sarcomere Z-disc filament filament Z-disc In cardiac and skeletal muscle cells, thick (myosin-containing) Key filaments and thin (actin-containing) filaments are organized into regular repeating units called the muscle sarcomere. Titin (centres thick filament and regulates its length) A single sarcomere extends from one Z-disc to the next. Tropomyosin/Troponin The stripes in H&E stained longitudinal sections shown above Tropomodulin (’caps’ end of thin filaments) (1c) show the end-to-end arrangement of many muscle α-actinin sarcomeres along the fiber. -
Kumka's Response to Stecco's Fascial Nomenclature Editorial
Journal of Bodywork & Movement Therapies (2014) 18, 591e598 Available online at www.sciencedirect.com ScienceDirect journal homepage: www.elsevier.com/jbmt FASCIA SCIENCE AND CLINICAL APPLICATIONS: RESPONSE Kumka’s response to Stecco’s fascial nomenclature editorial Myroslava Kumka, MD, PhD* Canadian Memorial Chiropractic College, Department of Anatomy, 6100 Leslie Street, Toronto, ON M2H 3J1, Canada Received 12 May 2014; received in revised form 13 May 2014; accepted 26 June 2014 Why are there so many discussions? response to the direction of various strains and stimuli. (De Zordo et al., 2009) Embedded with a range of mechanore- The clinical importance of fasciae (involvement in patho- ceptors and free nerve endings, it appears fascia has a role in logical conditions, manipulation, treatment) makes the proprioception, muscle tonicity, and pain generation. fascial system a subject of investigation using techniques (Schleip et al., 2005) Pathology and injury of fascia could ranging from direct imaging and dissections to in vitro potentially lead to modification of the entire efficiency of cellular modeling and mathematical algorithms (Chaudhry the locomotor system (van der Wal and Pubmed Exact, 2009). et al., 2008; Langevin et al., 2007). Despite being a topic of growing interest worldwide, This tissue is important for all manual therapists as a controversies still exist regarding the official definition, pain generator and potentially treatable entity through soft terminology, classification and clinical significance of fascia tissue and joint manipulative techniques. (Day et al., 2009) (Langevin et al., 2009; Mirkin, 2008). It is also reportedly treated with therapeutic modalities Lack of consistent terminology has a negative effect on such as therapeutic ultrasound, microcurrent, low level international communication within and outside many laser, acupuncture, and extracorporeal shockwave therapy. -
Structure and Function of Connective Tissue in Cardiac Muscle: Collagen Types I and III in Endomysial Struts and Pericellular Fibers
Scanning Microscopy Volume 2 Number 2 Article 33 2-10-1988 Structure and Function of Connective Tissue in Cardiac Muscle: Collagen Types I and III in Endomysial Struts and Pericellular Fibers Thomas F. Robinson Albert Einstein College of Medicine Leona Cohen-Gould Albert Einstein College of Medicine Stephen M. Factor Albert Einstein College of Medicine Mahboubeh Eghbali Albert Einstein College of Medicine Olga O. Blumenfeld Albert Einstein College of Medicine Follow this and additional works at: https://digitalcommons.usu.edu/microscopy Part of the Life Sciences Commons Recommended Citation Robinson, Thomas F.; Cohen-Gould, Leona; Factor, Stephen M.; Eghbali, Mahboubeh; and Blumenfeld, Olga O. (1988) "Structure and Function of Connective Tissue in Cardiac Muscle: Collagen Types I and III in Endomysial Struts and Pericellular Fibers," Scanning Microscopy: Vol. 2 : No. 2 , Article 33. Available at: https://digitalcommons.usu.edu/microscopy/vol2/iss2/33 This Article is brought to you for free and open access by the Western Dairy Center at DigitalCommons@USU. It has been accepted for inclusion in Scanning Microscopy by an authorized administrator of DigitalCommons@USU. For more information, please contact [email protected]. Scanning Microscopy, Vol. 2, No. 2, 1988 (Pages 1005-1015) 0891-7035/88$3.00+.00 Scanning Microscopy International, Chicago (AMF O'Hare), IL 60666 USA STRUCTURE AND FUNCTION OF CONNECTIVE TISSUE IN CARDIAC MUSCLE: COLLAGEN TYPES I and III IN ENDOMYSIAL STRUTS AND PERICELLULAR FIBERS Thomas F. Robinsonl,2 *, Leona Cohen-Gouldl -
Lab-Muscle-2018.Pdf
Introduction Remember those four Basic Tissues? Here they are again: 1. Epithelial tissue 2. Connective tissues 3. Muscle tissue 4. Nervous tissue During this lab you will learn about the third Basic Tissues: Muscle. Muscle comes in three different flavors: smooth, cardiac and skeletal. You need to be able to recognize each type of muscle and also differentiate from other tissues that it may easily be confused with (such as connective tissue), which takes practice. Learning objectives and activities Using the Virtual Slidebox: A Identify the connective tissue component of skeletal muscle Examine the organization of connective tissue within a whole skeletal muscle. B Differentiate between muscle types Identify and distinguish between smooth, skeletal and cardiac muscle histologically in both longitudinal and transverse section. C Decipher an EM of a sarcomere Decipher the pattern of proteins that form a sarcomere by interpreting an electron micrograph of skeletal muscle. D Test your skills Complete the self-quiz to test your understanding and master your learning. IDENTIFY THE CONNECTIVE TISSUE COMPONENT OF SKELETAL MUSCLE i. Tendon Examine Slide 1(15) to review the structure of a tendon. i. Dense regular connective tissue and accompanying fibroblasts. Recall why this organization is the most optimal for a tendon. ii. ii. Deep fascia Examine Slide 2a (13) and Slide 3a to approximate the location of deep fascia. iii. Dense regular/irregular connective tissue that separates muscles into compartments. This layer is best seen in gross anatomy and is not iv. observed in these specimens. iii. Epimysium Examine Slide 2a (13) and Slide 3a to locate the epimysium. -
Fascia: a Morphological Description and Classification System Based on a Literature Review Myroslava Kumka, MD, Phd* Jason Bonar, Bsckin, DC
0008-3194/2012/179–191/$2.00/©JCCA 2012 Fascia: a morphological description and classification system based on a literature review Myroslava Kumka, MD, PhD* Jason Bonar, BScKin, DC Fascia is virtually inseparable from all structures in Le fascia est pratiquement inséparable de toutes les the body and acts to create continuity amongst tissues structures du corps, et il sert à créer une continuité to enhance function and support. In the past fascia entre les tissus afin d’en améliorer la fonction et le has been difficult to study leading to ambiguities in soutien. Il a déjà été difficile d’étudier le fascia, ce qui nomenclature, which have only recently been addressed. a donné lieu à des ambiguïtés dans la nomenclature, Through review of the available literature, advances qui n’ont été abordées que récemment. Grâce à un in fascia research were compiled, and issues related examen de la documentation disponible, les avancées to terminology, descriptions, and clinical relevance of dans la recherche sur le fascia ont été compilées, fascia were addressed. Our multimodal search strategy et les problèmes relevant de la terminologie, des was conducted in Medline and PubMed databases, with descriptions et de la pertinence clinique du fascia ont été other targeted searches in Google Scholar and by hand, traités. Nous avons adopté une stratégie de recherche utilizing reference lists and conference proceedings. multimodale pour nos recherches dans les bases de In an effort to organize nomenclature for fascial données Medline et PubMed, avec des recherches ciblées structures provided by the Federative International dans Google Scholar et manuelles, au moyen de listes de Committee on Anatomical Terminology (FICAT), we références et de comptes rendus de congrès. -
Histological Aspects of Skeletal Muscle Fibers Splitting of C57BL/6Ncrl Mice
Physiol. Res. 69: 291-296, 2020 https://doi.org/10.33549/physiolres.934245 Histological Aspects of Skeletal Muscle Fibers Splitting of C57BL/6NCrl Mice Peter MAKOVICKÝ1, Pavol MAKOVICKÝ2 1Czech Centre for Phenogenomics, Institute of Molecular Genetic of the Czech Academy of Sciences, Vestec, Czech Republic. 2Department of Biology, Faculty of Education, J. Selye University, Komarno, Slovak Republic Received July 1, 2019 Accepted November 28, 2019 Epub Ahead of Print March 23, 2020 Summary orchestrated process and the factors that impact skeletal The objective of the current study is to present data on the muscle structure, function and regeneration are of great splitting of skeletal muscle fibers in C57BL/6NCrl mice. Skeletal importance and interest not only scientifically but also muscles (m. rectus femoris (m. quadriceps femoris)) from 500 clinically. This means, skeletal muscles regeneration is in (250 ♀ and 250 ♂) C57BL/6NCrl mice in the 16th week of life the interest of medical research (Kinter and Sinnreich were sampled during autopsy and afterwards standardly 2014, Liu et al. 2018). Today skeletal muscle histologically processed. Results show spontaneous skeletal regeneration is studied at a high level including injury, muscle fiber splitting which is followed by skeletal muscle fiber development, factors contributing to regeneration, regeneration. One solitary skeletal muscle fiber is split, or is in satellite cells, stem cells, the role of secreted factors and contact with few localized splitting skeletal muscle fibers. Part of extracellular matrix remodelling (Baghdadi and the split skeletal muscular fiber is phagocytosed, but the Tajbakhsh 2018, Liu et al. 2019, Wosczyna et al. 2019). remaining skeletal muscular fiber splits are merged into one The results are important for applied research and regenerating skeletal muscle fiber. -
Skeletal Muscle
Muscle 解剖學暨細胞生物學研究所 黃敏銓 基醫大樓6樓 0646室 [email protected] 1 Single-cell contractile units Multicellular contractile units • Myoepithelial cells • Smooth muscle – Expel secretion from • Striated muscle glandular acini – Skeletal muscle • Pericytes – Surround blood vessels – Visceral striated muscle • Myofibroblast Tongue, pharynx, diaphragm, esophagus – A dominant cell type in formation of a scar – Cardiac muscle 2 Skeletal muscle • Muscle fibers: extremely elongated, multinucleate contractile cells, bound by collagenous supporting tissue – Individual muscle fiber: 10-100 m in diameter, may reach up to 35 cm in length • Motor unit: the motor neuron and the muscle fibers it supplies – Vitality of skeletal muscle fibers is dependent on the maintenance of their nerve supply 3 Muscle fibers (cells) Skeletal muscle Muscle fiber (muscle cell) Myofibril Sarcomere Thick filament Thin filament (myosin filament) (actin filament) Molecules: Molecule: Actin myosin Tropomyosin 4 Troponin complex Skeletal muscle Connective tissues: endomysium, perimysium, epimysium Blood vessels and nerves (肌束) Endomysium • Small fasciculi: external muscles of the eye • Large fasciculi: the muscle of the buttocks 5 * Fasciculus = Fascicle Skeletal muscle ─ fasciculus Trichrome stain X150 muscle cells (fibers) endomysium 1. Reticulin fibers 2. collagen N: nerve bundle V: blood vessel 6 Basal lamina stained by silver stain Reticular fiber 7 Skeletal muscle ─ fasciculi of the tongue Masson’s trichrome stain X300 TS: transverse section P: perimysium C: capillaries 8 Red: