Muscle Fibers
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0270.6474/84/0408-1933$02.00/O The Journal of Neuroscience Copyright 0 Society for Neuroscience Vol. 4, No. 8, pp. 1933-1943 Printed in U.S.A. August 1984 PARTIAL PURIFICATION AND FUNCTIONAL IDENTIFICATION OF A CALMODULIN-ACTIVATED, ADENOSINE 5’-TRIPHOSPHATE-DEPENDENT CALCIUM PUMP FROM SYNAPTIC PLASMA MEMBRANES1 DIANE M. PAPAZIAN,* HANNAH RAHAMIMOFF,$ AND STANLEY M. GOLDIN§’ Departments of *Biological Chemistry and $Pharmacology, Harvard Medical School, Boston, Massachusetts 02115 and *Department of Biochemistry, Hadassah Medical School, Hebrew University, Jerusalem, Israel Received July 18, 1983; Revised February 27, 1984; Accepted February 28, 1984 Abstract Synaptic plasma membranes isolated from rat brain contain a calmodulin-activated Ca2+ pump. It has been purified 80- to 160-fold by solubilization with Triton X-100 and affinity chromatography on a calmodulin- Sepharose 4B column. After reconstitution into phospholipid vesicles, the affinity-purified pump efficiently catalyzed ATP dependent Ca2+ transport, which was activated 7- to g-fold by calmodulin. The major protein component of the affinity-purified preparation had a M, = 140,000; it was virtually the only band visualized on a Coomassie blue-stained SDS polyacrylamide gel. It has been identified as the Ca”’ pump by two functional criteria. First, it was phosphorylated by [y-““P]ATP in a Ca’+-dependent manner; the phosphorylated protein had the chemical reactivity of an acyl phosphate, characteristic of the phosphorylated intermediates of ion-transporting ATPases. Second, the protein was enriched by transport-specific fractiona- tion, a density gradient procedure which uses the transport properties of the reconstituted Ca2+ pump as a physical tool for its purification. -
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. -
VIEW Open Access Muscle Spindle Function in Healthy and Diseased Muscle Stephan Kröger* and Bridgette Watkins
Kröger and Watkins Skeletal Muscle (2021) 11:3 https://doi.org/10.1186/s13395-020-00258-x REVIEW Open Access Muscle spindle function in healthy and diseased muscle Stephan Kröger* and Bridgette Watkins Abstract Almost every muscle contains muscle spindles. These delicate sensory receptors inform the central nervous system (CNS) about changes in the length of individual muscles and the speed of stretching. With this information, the CNS computes the position and movement of our extremities in space, which is a requirement for motor control, for maintaining posture and for a stable gait. Many neuromuscular diseases affect muscle spindle function contributing, among others, to an unstable gait, frequent falls and ataxic behavior in the affected patients. Nevertheless, muscle spindles are usually ignored during examination and analysis of muscle function and when designing therapeutic strategies for neuromuscular diseases. This review summarizes the development and function of muscle spindles and the changes observed under pathological conditions, in particular in the various forms of muscular dystrophies. Keywords: Mechanotransduction, Sensory physiology, Proprioception, Neuromuscular diseases, Intrafusal fibers, Muscular dystrophy In its original sense, the term proprioception refers to development of head control and walking, an early im- sensory information arising in our own musculoskeletal pairment of fine motor skills, sensory ataxia with un- system itself [1–4]. Proprioceptive information informs steady gait, increased stride-to-stride variability in force us about the contractile state and movement of muscles, and step length, an inability to maintain balance with about muscle force, heaviness, stiffness, viscosity and ef- eyes closed (Romberg’s sign), a severely reduced ability fort and, thus, is required for any coordinated move- to identify the direction of joint movements, and an ab- ment, normal gait and for the maintenance of a stable sence of tendon reflexes [6–12]. -
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. -
4 Muscle Tissue Smooth Muscle
4 Muscle tissue Smooth muscle Smooth muscle cell bundle (oblique section) Loose connective tissue layer permitting movement between muscle layers Elongated centrally located nucleus of smooth muscle cell (longitudinal section) Elongated, tapering cytoplasm of a smooth muscle cell Smooth muscle, small intestine, cat. H.E. stain; x400. Perimysium composed of connective tissue with blood vessels and autonomic nerves Smooth muscle cell bundle with central nuclei and elongated cytoplasm (longitudinal section) Perimysium Oblique and cross sections of smooth muscle cells Smooth muscle, small intestine, cat. H.E. stain; x400. Smooth muscle cells (oblique and cross sections) Smooth muscle cells (cross section) Perimysium Smooth muscle, urinary bladder, cat. H.E. stain; x350. 4 Muscle tissue Smooth muscle Predominantly longitudinally oriented smooth muscle fibre bundles closely invested with endomysium (nuclei appear longitudinally oval) Perimysium Endomysium Predominantly transversely oriented smooth muscle fibre bundles (nuclei appear round) Sooth muscle, urinary bladder, cat. Golder's Masson trichrome stain; x480. Nucleus of smooth muscle cell (weakly contracted) Perimysium with fibrocytes Cytoplasm of smooth muscle cell (weakly contracted) Nuclei and cytoplasm of smooth muscle cells (relaxed) Endomysium surrounding isolated smooth muscle cell (at transition to perimysium) Perimysium with fibrocytes Smooth muscle, urinary bladder, cat. H.E. stain; Goldner's Masson trichrome stain; x480. Central nucleus and cytoplasm of weakly contracted smooth muscle cell Heterochromatic nucleus of smooth muscle cell Endomysium Perimysium with fibrocytes Euchromatic nucleus of smooth muscle cell with spindle-like elongation of cytoplasm Smooth muscle, gall bladder, ox. Goldner's stain; x600.. -
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. -
A Device to Measure Tensile Forces in the Deep Fascia of the Human Abdominal Wall
A Device to Measure Tensile Forces in the Deep Fascia of the Human Abdominal Wall Sponsored by Dr. Raymond Dunn of the University of Massachusetts Medical School A Major Qualifying Report Submitted to the Faculty Of the WORCESTER POLYTECHNIC INSTITUTE In partial fulfillment of the requirements for the Degree of Bachelor of Science By Olivia Doane _______________________ Claudia Lee _______________________ Meredith Saucier _______________________ April 18, 2013 Advisor: Professor Kristen Billiar _______________________ Co-Advisor: Dr. Raymond Dunn _______________________ Table of Contents Table of Figures ............................................................................................................................. iv List of Tables ................................................................................................................................. vi Authorship Page ............................................................................................................................ vii Acknowledgements ...................................................................................................................... viii Abstract .......................................................................................................................................... ix Chapter 1: Introduction ................................................................................................................... 1 Chapter 2: Literature Review ......................................................................................................... -
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. -
Fascial Contraction Fascia Can Be Divided Into Two General Categories: Sub Cutaneous Fascia and Deep Fascia, Also Known As Muscu Lar Fascia
by joe muscolino body mechanics Bodywork and movement therapy can help with contracted fascial tissue. fascial contraction Fascia can be divided into two general categories: sub- examples of deep fibrous fascia, as cutaneous fascia and deep fascia, also known as muscu- are ligaments and intermuscular lar fascia. Subcutaneous fascia, as the name implies, is septa. The loosely packed struc- located immediately deep to the skin. It is largely com- ture of subcutaneous fascia allows www.amtamassage.org/mtj posed of adipose (fat) cells, giving it its gel-like consis- for a healthy blood supply, giving it tency. Collagen fibers and fibroblast cells are embedded strong reparative properties when within this mix of adipose cells. Deep fascia is located injured. Alternatively, the dense ar- deeper in the body and is primarily comprised of dense- rangement of fibrous fascia does not ly packed collagen fibers, accounting for its description allow adequate room for blood ves- as fibrous fascia. Fibroblasts are located between these sels; therefore, fibrous fascia has a collagen fibers (Figure 1). poor blood supply and does not heal Endomysium, perimysium and epimysium, which well when injured. In addition to 145 create the tendons and aponeuroses of muscles, are collagen fibers and fibroblasts, both body mechanics Recent research suggests that fascia does and stretched, having the ability to transfer these pull- ing forces to other tissues. For example, when a muscle not function only in a belly contracts and pulls upon its tendons, these fibrous passive tensile manner, tissue tendons transfer that pulling force to the bony at- tachments of the muscle. -
MODULE 1: HISTOLOGY I an Introduction to Histology; Begin Epithelial Tissue and Connective Tissue
MODULE 1: HISTOLOGY I An Introduction to Histology; Begin Epithelial Tissue and Connective Tissue Histology is the study of the microscopic anatomy of the cells and extracellular matrix that make up the tissues of the body. Using the physical appearance of cells and the matrix that surrounds them, the 10-100 trillion cells of the human body can be grouped into just four major tissue types: epithelial, connective, muscle and nervous tissues. In the Histology Modules of this course, you will learn to identify each of these tissue types as well as their subclasses and important structures. Chemical fixatives are used to preserve tissues when they are harvested. These fixatives are important to preserve the tissue from degradation. These chemicals also destroy the biological function of the cells, so all of the cells in any micrograph images that you see are dead. Biological tissue has little inherent color. In fact, in reality, the tissues that you study would look transparent or have various shades of gray for the most part. However, scientists use staining techniques to help highlight particular features of a tissue. As a student of histology, you should avoid the temptation to memorize tissues based on color. Since it is possible to stain the same tissue with a variety of different colors, you could be easily fooled if you trained yourself to recognize color as the major feature of tissues that you study. The wiser approach would be to carefully learn the shapes and physical characteristics other than color when studying histology. Students who memorize color as the main characteristic to trigger their memory will be disappointed when the exam does not maintain color schemes. -
Laboratory Methodology for the Histological Study of Skeletal Muscle
ReviewArtículo original Laboratory methodology for the histological study of skeletal muscle Fernando Leiva-Cepas1,2,3, Ignacio Ruz-Caracuel1,2*, María A. Peña-Toledo2,3, Antonio Agüera-Vega1,2, Ignacio Jimena1,2,3, Evelio Luque1,3, José Peña1,2,3 1Departamento de Ciencias Morfológicas. Universidad de Córdoba. Córdoba. 2Grupo de Investigación en Regeneración Muscular. Universidad de Córdoba. 3Instituto Maimónides de Investigación Biomédica de Córdoba. IMIBIC. Córdoba. *Servicio de Anatomía Patológica. Hospital Universitario La Paz, IDIPAZ, Madrid. Received: 11.12.2017 Summary Accepted: 15.02.2018 Skeletal muscle is a malleable and dynamic tissue capable of a high degree of plasticity in regards to its histological confi- guration. In this sense, microscopic study is an important and essential tool for the analysis of adaptive processes -such as hypertrophy or changes of fiber types- and the regeneration or repair of skeletal muscle after injury, in the fields of sports medicine and traumatology respectively. While light microscopy addresses the study of the different constitutive elements into the skeletal muscle and their relationships with each other that determine the organ histoarchitecture, with electron microscopy an ultrastructural analysis is carried out that allows to relate the structure and function of the individual cells. This article illustrates a pragmatic and practical approach, based on personal experience and a review of the literature, from the conditions in obtaining and sending samples of skeletal muscle to the laboratory to the procedures to prepare them for histological study (sections of cryostat, paraffin sections and electron microscopy). Especially we focus on the description of Key words: the processing by freezing and recommendations to follow, as this is the ideal method for this tissue.