Muscle Tissue 1) Striated Skeletal Muscle Tissue
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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]. -
Desmin- Cytoskeleton Marker Cat#: ET1606-30
rev. 04/13/16 Desmin- Cytoskeleton Marker Cat#: ET1606-30 Prod uct Type: R ecombinant r abbit mono clonal IgG, primary antibodies Species reactivity: Human, Mouse, Rat, Zebra fish Applications: WB, ICC/IF, IHC, FC Molecular Wt.: 53 kDa Description: Cytoskeletal intermediate filaments (IFs) constitute a diverse group of proteins that are expressed in a highly tissue - specific manner. IFs are constructed from two - chain α -helical coiled-coil molecules arranged on an imperfect helical Fig1: Western blot analysis of Desmin on lattice, and have been widely used as markers for distinguishing different lysates using anti-Desmin antibody at individual cell types within a tissue and identifying the origins 1/1,000 dilution. of metastatic tumors. Vimentin is an IF general marker of cells Positive control: originating in the mesenchyme. Vimentin and Desmin, a related class III IF, are both expressed during skeletal muscle development. Lane 1: Human skeletal muscle Desmin, a 469 amino acid protein found near the Z line in sarcomeres, Lane 2: Mouse heart is expressed more frequently in adult differentiated state tissues. Desmin makes up attachments between the terminal Z-disc and membrane-associated proteins to form a force-transmitting system. Mutations in the gene encoding for Desmin are associated with adult-onset skeletal myopathy, sporadic disease and mild cardiac involvement. Immunogen: Recombinant protein. Positive control: Fig2: ICC staining Desmin in C2C12 cells (green). C2C12, human uterus tissue, mouse bladder tissue, mouse heart The nuclear counter stain is DAPI (blue). Cells tissue, mouse skeletal muscle tissue. were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. -
The Muscular System
THE MUSCULAR SYSTEM COMPILED BY HOWIE BAUM 1 Muscles make up the bulk of the body and account for 1/3 of its weight.!! Blood vessels and nerves run to every muscle, helping control and regulate each muscle’s function. The muscular system creates body heat and also moves the: Bones of the Skeletal system Food through Digestive system Blood through the Circulatory system Fluids through the Excretory system MUSCLE TISSUE The body has 3 main types of muscle tissue 1) Skeletal, 2) Smooth, and 3) Cardiac SKELETAL MUSCLE SMOOTH MUSCLE CARDIAC MUSCLE Skeletal muscles attach to and move bones by contracting and relaxing in response to voluntary messages from the nervous system. Skeletal muscle tissue is composed of long cells called muscle fibers that have a striated appearance. Muscle fibers are organized into bundles supplied by blood vessels and innervated by motor neurons. Muscle structure Skeletal (striated or voluntary) muscle consists of densely packed groups of hugely elongated cells known as myofibers. These are grouped into bundles (fascicles). A typical myofiber is 2–3 centimeters ( 3/4–1 1/5 in) long and 0.05millimeters (1/500 inch) in diameter and is composed of narrower structures – myofibrils. These contain thick and thin myofilaments made up mainly of the proteins actin and myosin. Numerous capillaries keep the muscle supplied with the oxygen and glucose needed to fuel contraction. Skeletal Muscles • Skeletal muscles attach to bones by tendons (connective tissue) and enable movement. • Skeletal muscles are mostly voluntary Feel the back of your ankle to feel your Achilles tendon - the largest tendon in your body. -
Muscle Histology
Muscle Histology Dr. Heba Kalbouneh Functions of muscle tissue ▪ Movement ▪ Maintenance of posture ▪ Joint stabilization ▪ Heat generation Types of Muscle Tissue ▪ Skeletal muscle ▪ Cardiac muscle ▪ Smooth muscle Types of Muscle Tissue Skeletal •Attach to and move skeleton •40% of body weight •Fibers = multinucleate cells (embryonic cells fuse) •Cells with obvious striations •Contractions are voluntary Cardiac: only in the wall of the heart •Cells are striated •Contractions are involuntary (not voluntary) Smooth: walls of hollow organs •Lack striations •Contractions are involuntary (not voluntary) Similarities… ▪ Their cells are called fibers because they are elongated ▪ Contraction depends on myofilaments ▪ Actin ▪ Myosin ▪ Plasma membrane is called sarcolemma ▪ Sarcos = flesh ▪ Lemma = sheath SKELETAL MUSCLES Epimysium: surrounds whole muscle Endomysium is around each muscle fiber Perimysium is around fascicle = muscle cell= myofiber Skeletal muscle This big cylinder is a fiber: a cell ▪ Fibers (each is one cell) have striations ▪ Myofibrils are organelles of the cell: these are made -an organelle up of myofilaments ▪ Sarcomere ▪ Basic unit of contraction ▪ Myofibrils are long rows of repeating sarcomeres ▪ Boundaries: Z discs (or lines) Sarcomere M line provides an attachment to myosin filaments Z line provides an attachment to actin filaments A band is the darker band of the myofibril containing myosin filaments H band is the lighter section in the middle of the A band where only myosin is present I band is the lighter band containing -
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. -
Evidence for the Nonmuscle Nature of The" Myofibroblast" of Granulation Tissue and Hypertropic Scar. an Immunofluorescence Study
American Journal of Pathology, Vol. 130, No. 2, February 1988 Copyright i American Association of Pathologists Evidencefor the Nonmuscle Nature ofthe "Myofibroblast" ofGranulation Tissue and Hypertropic Scar An Immunofluorescence Study ROBERT J. EDDY, BSc, JANE A. PETRO, MD, From the Department ofAnatomy, the Department ofSurgery, and JAMES J. TOMASEK, PhD Division ofPlastic and Reconstructive Surgery, and the Department of Orthopaedic Surgery, New York Medical College, Valhalla, New York Contraction is an important phenomenon in wound cell-matrix attachment in smooth muscle and non- repair and hypertrophic scarring. Studies indicate that muscle cells, respectively. Myofibroblasts can be iden- wound contraction involves a specialized cell known as tified by their intense staining of actin bundles with the myofibroblast, which has morphologic character- either anti-actin antibody or NBD-phallacidin. Myofi- istics of both smooth muscle and fibroblastic cells. In broblasts in all tissues stained for nonmuscle but not order to better characterize the myofibroblast, the au- smooth muscle myosin. In addition, nonmuscle myo- thors have examined its cytoskeleton and surrounding sin was localized as intracellular fibrils, which suggests extracellular matrix (ECM) in human burn granula- their similarity to stress fibers in cultured fibroblasts. tion tissue, human hypertrophic scar, and rat granula- The ECM around myofibroblasts stains intensely for tion tissue by indirect immunofluorescence. Primary fibronectin but lacks laminin, which suggests that a antibodies used in this study were directed against 1) true basal lamina is not present. The immunocytoche- smooth muscle myosin and 2) nonmuscle myosin, mical findings suggest that the myofibroblast is a spe- components ofthe cytoskeleton in smooth muscle and cialized nonmuscle type of cell, not a smooth muscle nonmuscle cells, respectively, and 3) laminin and 4) cell. -
Muscle Physiology Dr
Muscle Physiology Dr. Ebneshahidi Copyright © 2004 Pearson Education, Inc., publishing as Benjamin Cummings Skeletal Muscle Figure 9.2 (a) Copyright © 2004 Pearson Education, Inc., publishing as Benjamin Cummings Functions of the muscular system . 1. Locomotion . 2. Vasoconstriction and vasodilatation- constriction and dilation of blood vessel Walls are the results of smooth muscle contraction. 3. Peristalsis – wavelike motion along the digestive tract is produced by the Smooth muscle. 4. Cardiac motion . 5. Posture maintenance- contraction of skeletal muscles maintains body posture and muscle tone. 6. Heat generation – about 75% of ATP energy used in muscle contraction is released as heat. Copyright. © 2004 Pearson Education, Inc., publishing as Benjamin Cummings . Striation: only present in skeletal and cardiac muscles. Absent in smooth muscle. Nucleus: smooth and cardiac muscles are uninculcated (one nucleus per cell), skeletal muscle is multinucleated (several nuclei per cell ). Transverse tubule ( T tubule ): well developed in skeletal and cardiac muscles to transport calcium. Absent in smooth muscle. Intercalated disk: specialized intercellular junction that only occurs in cardiac muscle. Control: skeletal muscle is always under voluntary control‚ with some exceptions ( the tongue and pili arrector muscles in the dermis). smooth and cardiac muscles are under involuntary control. Copyright © 2004 Pearson Education, Inc., publishing as Benjamin Cummings Innervation: motor unit . a) a motor nerve and a myofibril from a neuromuscular junction where gap (called synapse) occurs between the two structures. at the end of motor nerve‚ neurotransmitter (i.e. acetylcholine) is stored in synaptic vesicles which will release the neurotransmitter using exocytosis upon the stimulation of a nerve impulse. Across the synapse the surface the of myofibril contains receptors that can bind with the neurotransmitter. -
Massive Alterations of Sarcoplasmic Reticulum Free Calcium in Skeletal Muscle Fibers Lacking Calsequestrin Revealed by a Genetic
Massive alterations of sarcoplasmic reticulum free calcium in skeletal muscle fibers lacking calsequestrin revealed by a genetically encoded probe M. Canatoa,1, M. Scorzetoa,1, M. Giacomellob, F. Protasic,d, C. Reggiania,d, and G. J. M. Stienene,2 Departments of aHuman Anatomy and Physiology and bExperimental Veterinary Sciences, University of Padua, 35121 Padua, Italy; cCeSI, Department of Basic and Applied Medical Sciences, University G. d’Annunzio, I-66013 Chieti, Italy; dIIM-Interuniversity Institute of Myology and eLaboratory for Physiology, Institute for Cardiovascular Research, VU University Medical Center, 1081BT, Amsterdam, The Netherlands Edited* by Clara Franzini-Armstrong, University of Pennsylvania Medical Center, Philadelphia, PA, and approved November 12, 2010 (received for review June 30, 2010) The cytosolic free Ca2+ transients elicited by muscle fiber excitation tion essential to maintain a low metabolic rate in quiescent ex- are well characterized, but little is known about the free [Ca2+] citable cells. In addition, CSQ has been shown to modulate RyR- dynamics within the sarcoplasmic reticulum (SR). A targetable mediated Ca2+ release from the SR (6). To understand the pivotal ratiometric FRET-based calcium indicator (D1ER Cameleon) allowed role of CSQ in SR function, it is critical to determine free SR us to investigate SR Ca2+ dynamics and analyze the impact of cal- Ca2+ concentration, and this has been made possible by the ad- sequestrin (CSQ) on SR [Ca2+] in enzymatically dissociated flexor vent of a targetable ratiometric FRET-based indicator, such as digitorum brevis muscle fibers from WT and CSQ-KO mice lacking D1ER Cameleon (7). Seminal studies using this technique have isoform 1 (CSQ-KO) or both isoforms [CSQ-double KO (DKO)]. -
Localization of Ca2l Release Channels with Ryanodine in Junctional
Proc. NatI. Acad. Sci. USA Vol. 82, pp. 7256-7259, November 1985 Biochemistry Localization of Ca2l release channels with ryanodine in junctional terminal cisternae of sarcoplasmic reticulum of fast skeletal muscle (muscle contraction/excitation-contraction coupling/ruthenium red/longitudinal cisternae/gated channels) SIDNEY FLEISCHER, EUNICE M. OGUNBUNMI, MARK C. DIXON, AND EDUARD A. M. FLEER Department of Molecular Biology, Vanderbilt University, Nashville, TN 37235 Communicated by William J. Darby, July 8, 198S ABSTRACT The mechanism of Ca2' release from tional terminal cisternae consist of two types of membranes, sarcoplasmic reticulum, which triggers contraction in skeletal the Ca2l pump membrane (80-85%) and the junctional face muscle, remains the key unresolved problem in excita- membrane (15-20%) (16). A unique characteristic of junc- tion-contraction coupling. Recently, we have described the tional terminal cisternae is that they have a poor Ca2+ loading isolation of purified fractions referable to terminal and longi- rate, which can be enhanced 5-fold or more by addition of tudinal cisternae of sarcoplasmic reticulum. Junctional termi- ruthenium red (RR) (ref. 17; unpublished data). This study nal cisternae are distinct in that they have a low net energized describes the drug action of ryanodine on the junctional Ca2+ loading, which can be enhanced 5-fold or more by terminal cisternae in blocking the action of RR. It provides addition of ruthenium red. The loading rate, normalized for evidence that the action of ryanodine is on the Ca2' release calcium pump protein content, then approaches that of longi- mechanism and supports the view that Ca2' release is tudinal cisternae of sarcoplasmic reticulum. -
Muscle Tissue
Muscle Tissue Dr. Heba Kalbouneh Associate Professor of Anatomy and Histology Functions of muscle tissue . Movement . Maintenance of posture . Joint stabilization . Heat generation Tendon Dr. Heba Kalbouneh Dr. Belly Tendon Types of Muscle Tissue . Skeletal muscle . Cardiac muscle Dr. Heba Kalbouneh Dr. Smooth muscle Skeletal Attach to and move skeleton 40% of body weight Fibers = multinucleate cells (embryonic cells fuse) Cells with obvious striations Contractions are voluntary Cardiac: only in the wall of the heart Cells are striated Contractions are involuntary Dr. Heba Kalbouneh Dr. Smooth: walls of hollow organs Lack striations Contractions are involuntary . Their cells are called fibers because they are elongated Similarities… . Contraction depends on myofilaments . Actin . Myosin . Plasma membrane is called sarcolemma . Sarkos = flesh . Lemma = sheath Skeletal muscle Cardiac muscle Smooth muscle Dr. Heba Kalbouneh Dr. Skeletal muscle Epimysium surrounds whole muscle Endomysium is around each Dr. Heba Kalbouneh Dr. muscle fiber Perimysium is around fascicle Epimysium Fascicle Fascicle Fascicle Fascicle Fascicle Dr. Heba Kalbouneh Dr. Fascicle Perimysium Cell Cell Cell Dr. Heba Kalbouneh Dr. Cell Cell Endomysium Dr. Heba Kalbouneh Dr. Muscle fiber== musclemuscle cell=cell= myofibermyofiber Skeletal muscle This big cylinder is a fiber: a cell Fibers (each is one cell) have striations Myofibril is an organelle Myofibrils are organelles of the cell, are made up of myofilaments Myofibrils are long rows of repeating Dr. Heba Kalbouneh -
Ultra-High Resolution Scanning Electron Microscopic Studies on the Sarcoplasmic Reticulum and Mitochondria in Various Muscles: a Review
Scanning Microscopy Volume 7 Number 1 Article 16 12-29-1992 Ultra-High Resolution Scanning Electron Microscopic Studies on the Sarcoplasmic Reticulum and Mitochondria in Various Muscles: A Review Takuro Ogata Kochi Medical School Yuichi Yamasaki Kochi Medical School Follow this and additional works at: https://digitalcommons.usu.edu/microscopy Part of the Biology Commons Recommended Citation Ogata, Takuro and Yamasaki, Yuichi (1992) "Ultra-High Resolution Scanning Electron Microscopic Studies on the Sarcoplasmic Reticulum and Mitochondria in Various Muscles: A Review," Scanning Microscopy: Vol. 7 : No. 1 , Article 16. Available at: https://digitalcommons.usu.edu/microscopy/vol7/iss1/16 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. 7, No. 1, 1993 (Pages 145-156) 0891-7035/93$5 .00+ .00 Scanning Microscopy International, Chicago (AMF O'Hare), IL 60666 USA ULTRA-HIGH RESOLUTION SCANNING ELECTRON MICROSCOPIC STUDIES ON THE SARCOPLASMIC RETICULUM AND MITOCHONDRIA IN VARIOUS MUSCLES: A REVIEW Takuro Ogata* and Yuichi Yamasaki Department of Surgery, Kochi Medical School Nankoku, Kochi, 783 Japan (Received for publication March 23, 1992, and in revised form December 29, 1992) Abstract Introduction The three-dimensional structure of the sarco The three-dimensional models of the membrane plasm.ic -
Titin N2A Domain and Its Interactions at the Sarcomere
International Journal of Molecular Sciences Review Titin N2A Domain and Its Interactions at the Sarcomere Adeleye O. Adewale and Young-Hoon Ahn * Department of Chemistry, Wayne State University, Detroit, MI 48202, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-(313)-577-1384 Abstract: Titin is a giant protein in the sarcomere that plays an essential role in muscle contraction with actin and myosin filaments. However, its utility goes beyond mechanical functions, extending to versatile and complex roles in sarcomere organization and maintenance, passive force, mechanosens- ing, and signaling. Titin’s multiple functions are in part attributed to its large size and modular structures that interact with a myriad of protein partners. Among titin’s domains, the N2A element is one of titin’s unique segments that contributes to titin’s functions in compliance, contraction, structural stability, and signaling via protein–protein interactions with actin filament, chaperones, stress-sensing proteins, and proteases. Considering the significance of N2A, this review highlights structural conformations of N2A, its predisposition for protein–protein interactions, and its multiple interacting protein partners that allow the modulation of titin’s biological effects. Lastly, the nature of N2A for interactions with chaperones and proteases is included, presenting it as an important node that impacts titin’s structural and functional integrity. Keywords: titin; N2A domain; protein–protein interaction 1. Introduction Citation: Adewale, A.O.; Ahn, Y.-H. The complexity of striated muscle is defined by the intricate organization of its com- Titin N2A Domain and Its ponents [1]. The involuntary cardiac and voluntary skeletal muscles are the primary types Interactions at the Sarcomere.