Structural Stages in the Development of the Long Bones and Epiphyses a STUDY in the NEW ZEALAND WHITE RABBIT
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Development of the Endochondral Skeleton
Downloaded from http://cshperspectives.cshlp.org/ on September 24, 2021 - Published by Cold Spring Harbor Laboratory Press Development of the Endochondral Skeleton Fanxin Long1,2 and David M. Ornitz2 1Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110 2Department of Developmental Biology, Washington University School of Medicine, St. Louis, Missouri 63110 Correspondence: fl[email protected] SUMMARY Much of the mammalian skeleton is composed of bones that originate from cartilage templates through endochondral ossification. Elucidating the mechanisms that control endochondral bone development is critical for understanding human skeletal diseases, injury response, and aging. Mouse genetic studies in the past 15 years have provided unprecedented insights about molecules regulating chondrocyte formation, chondrocyte maturation, and osteoblast differ- entiation, all key processes of endochondral bone development. These include the roles of the secreted proteins IHH, PTHrP, BMPs, WNTs, and FGFs, their receptors, and transcription factors such as SOX9, RUNX2, and OSX, in regulating chondrocyte and osteoblast biology. This review aims to integrate the known functions of extracellular signals and transcription factors that regulate development of the endochondral skeleton. Outline 1 Introduction 5 Osteoblastogenesis 2 Mesenchymal condensation 6 Closing remarks 3 Chondrocyte differentiation References 4 Growth plate development Editors: Patrick P.L. Tam, W. James Nelson, and Janet Rossant Additional Perspectives on Mammalian Development available at www.cshperspectives.org Copyright # 2013 Cold Spring Harbor Laboratory Press; all rights reserved; doi: 10.1101/cshperspect.a008334 Cite this article as Cold Spring Harb Perspect Biol 2013;5:a008334 1 Downloaded from http://cshperspectives.cshlp.org/ on September 24, 2021 - Published by Cold Spring Harbor Laboratory Press F. -
Intervertebral and Epiphyseal Fusion in the Postnatal Ontogeny of Cetaceans and Terrestrial Mammals
J Mammal Evol DOI 10.1007/s10914-014-9256-7 ORIGINAL PAPER Intervertebral and Epiphyseal Fusion in the Postnatal Ontogeny of Cetaceans and Terrestrial Mammals Meghan M. Moran & Sunil Bajpai & J. Craig George & Robert Suydam & Sharon Usip & J. G. M. Thewissen # Springer Science+Business Media New York 2014 Abstract In this paper we studied three related aspects of the Introduction ontogeny of the vertebral centrum of cetaceans and terrestrial mammals in an evolutionary context. We determined patterns The vertebral column provides support for the body and of ontogenetic fusion of the vertebral epiphyses in bowhead allows for flexibility and mobility (Gegenbaur and Bell whale (Balaena mysticetus) and beluga whale 1878;Hristovaetal.2011; Bruggeman et al. 2012). To (Delphinapterus leucas), comparing those to terrestrial mam- achieve this mobility, individual vertebrae articulate with each mals and Eocene cetaceans. We found that epiphyseal fusion other through cartilaginous intervertebral joints between the is initiated in the neck and the sacral region of terrestrial centra and synovial joints between the pre- and post- mammals, while in recent aquatic mammals epiphyseal fusion zygapophyses. The mobility of each vertebral joint varies is initiated in the neck and caudal regions, suggesting loco- greatly between species as well as along the vertebral column motor pattern and environment affect fusion pattern. We also within a single species. Vertebral column mobility greatly studied bony fusion of the sacrum and evaluated criteria used impacts locomotor style, whether the animal is terrestrial or to homologize cetacean vertebrae with the fused sacrum of aquatic. In aquatic Cetacea, buoyancy counteracts gravity, and terrestrial mammals. We found that the initial ossification of the tail is the main propulsive organ (Fish 1996;Fishetal. -
Upper Limb Development
Upper Limb Development Alphonsus Chong Department of Hand and Reconstructive Microsurgery National University Hospital Why bother? Most congenital limb anomalies are due to: Disorders of embryogenesis or Problems during fetal development Some terminology Embryogenesis 0-8 weeks – new organ systems appear Fetal period Appearance of primary ossification center in humerus Differentiation, maturation and enlargement of existing organs Limb Development Limb Patterning Tissue Differentiation Why is it an arm and not Skeletal a leg? Joint Vascular Nerve Muscle and Tendon Positional Information and Axes of the upper limb Limb Bud in E3 Chick Embryo Limb bud (lateral plate) Loose mesenchymal cells from lateral plate mesoderm Ectodermal epithelial cells Migrating cells Somites --> Muscle Nerves Vasculature Limb Bud Development Limb bud Ectoderm and mesenchyme Not fully differentiated yet but all ingredients there If transplanted ectopic limb Limb Bud Regions AER Progress zone Zone of polarizing activity AER – Proximal to Distal formation Zone of Polarizing Actvity – AP development Morphogen Gradient Model Dorsal / ventral patterning less well understood Separation of Digits Apoptosis (Programmed cell death) of interdigital mesenchyme BMPs important Starts post-axial to pre-axial Mesoderm specifies amount of apoptosis How does this relate to pathogensis? Picture from Greene Learning Points UE development occurs early in embryogenesis – most risk of development congenital anomalies Pattern of limb development follows a body plan Digit formation is by apoptosis Thank You Further Reading Principles of Development 3rd Ed by Lewis Wolpert. Oxford University Press Growing Hand. Amit Gupta and Louisville Group. -
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. -
GLOSSARY of MEDICAL and ANATOMICAL TERMS
GLOSSARY of MEDICAL and ANATOMICAL TERMS Abbreviations: • A. Arabic • abb. = abbreviation • c. circa = about • F. French • adj. adjective • G. Greek • Ge. German • cf. compare • L. Latin • dim. = diminutive • OF. Old French • ( ) plural form in brackets A-band abb. of anisotropic band G. anisos = unequal + tropos = turning; meaning having not equal properties in every direction; transverse bands in living skeletal muscle which rotate the plane of polarised light, cf. I-band. Abbé, Ernst. 1840-1905. German physicist; mathematical analysis of optics as a basis for constructing better microscopes; devised oil immersion lens; Abbé condenser. absorption L. absorbere = to suck up. acervulus L. = sand, gritty; brain sand (cf. psammoma body). acetylcholine an ester of choline found in many tissue, synapses & neuromuscular junctions, where it is a neural transmitter. acetylcholinesterase enzyme at motor end-plate responsible for rapid destruction of acetylcholine, a neurotransmitter. acidophilic adj. L. acidus = sour + G. philein = to love; affinity for an acidic dye, such as eosin staining cytoplasmic proteins. acinus (-i) L. = a juicy berry, a grape; applied to small, rounded terminal secretory units of compound exocrine glands that have a small lumen (adj. acinar). acrosome G. akron = extremity + soma = body; head of spermatozoon. actin polymer protein filament found in the intracellular cytoskeleton, particularly in the thin (I-) bands of striated muscle. adenohypophysis G. ade = an acorn + hypophyses = an undergrowth; anterior lobe of hypophysis (cf. pituitary). adenoid G. " + -oeides = in form of; in the form of a gland, glandular; the pharyngeal tonsil. adipocyte L. adeps = fat (of an animal) + G. kytos = a container; cells responsible for storage and metabolism of lipids, found in white fat and brown fat. -
Bone Markings / Features on Bones
08/05/2016 Bone Markings : Skeletal System Search Custom Search Like Tweet Home Health News Human Body Biology Chemistry Glossary Textbooks Bone Disorders Ads by Google ► Bone Tissue ► Bone Marrow ► Human Skull Bone ► Bone on Bone Knee Sun 8 May 2016 Bone Markings / Features on Bones Human Body Study Section Bone markings and the features of bones (including the correct words used to describe them) are often required by firstlevel courses in human anatomy and associated health science subjects. It is important to be familiar with the terminology used to Human Body Index refer to bone markings in order to communicate effectively with professionals involved in healthcare, research, forensics, and Health Glossary related disciplines. More about Bones and the Skeletal System: The following terms used to describe bone markings or features on bones are in alphabetical order with short definitions: Human Skeleton Axial and Appendicular Word / Term Meaning / Description Type of Example(s) Skeleton (Bone Marking or bone The Structure and Feature) marking Functions of Bones Types of Bones 1. Angle A corner Feature of Inferior angle (lower) and superior angle (upper) are Bone Markings & Features shape of bone the rounded angles or "corners" of the scapula. on Bones Disorders of the Skeletal 2. Body The main portion of a bone The diaphysis of long bones such as the humerus. System Curvature of the Spine 3. Condyle Rounded bump or large rounded Process The medial condyle of the femur (bone), upperleg. prominence. Such rounded surfaces forms joints Types of Joints usually fit into a fossa on another bone to Specific bones: form a joint. -
The Epiphyseal Plate: Physiology, Anatomy, and Trauma*
3 CE CREDITS CE Article The Epiphyseal Plate: Physiology, Anatomy, and Trauma* ❯❯ Dirsko J. F. von Pfeil, Abstract: This article reviews the development of long bones, the microanatomy and physiology Dr.med.vet, DVM, DACVS, of the growth plate, the closure times and contribution of different growth plates to overall growth, DECVS and the effect of, and prognosis for, traumatic injuries to the growth plate. Details on surgical Veterinary Specialists of Alaska Anchorage, Alaska treatment of growth plate fractures are beyond the scope of this article. ❯❯ Charles E. DeCamp, DVM, MS, DACVS athologic conditions affecting epi foramen. Growth factors and multipotent Michigan State University physeal (growth) plates in imma stem cells support the formation of neo ture animals may result in severe natal bone consisting of a central marrow P 2 orthopedic problems such as limb short cavity surrounded by a thin periosteum. ening, angular limb deformity, or joint The epiphysis is a secondary ossifica incongruity. Understanding growth plate tion center in the hyaline cartilage forming anatomy and physiology enables practic the joint surfaces at the proximal and distal At a Glance ing veterinarians to provide a prognosis ends of the bones. Secondary ossification Bone Formation and assess indications for surgery. Injured centers can appear in the fetus as early Page E1 animals should be closely observed dur as 28 days after conception1 (TABLE 1). Anatomy of the Growth ing the period of rapid growth. Growth of the epiphysis arises from two Plate areas: (1) the vascular reserve zone car Page E2 Bone Formation tilage, which is responsible for growth of Physiology of the Growth Bone is formed by transformation of con the epiphysis toward the joint, and (2) the Plate nective tissue (intramembranous ossifica epiphyseal plate, which is responsible for Page E4 tion) and replacement of a cartilaginous growth in bone length.3 The epiphyseal 1 Growth Plate Closure model (endochondral ossification). -
Homeobox Genes D11–D13 and A13 Control Mouse Autopod Cortical
Research article Homeobox genes d11–d13 and a13 control mouse autopod cortical bone and joint formation Pablo Villavicencio-Lorini,1,2 Pia Kuss,1,2 Julia Friedrich,1,2 Julia Haupt,1,2 Muhammed Farooq,3 Seval Türkmen,2 Denis Duboule,4 Jochen Hecht,1,5 and Stefan Mundlos1,2,5 1Max Planck Institute for Molecular Genetics, Berlin, Germany. 2Institute for Medical Genetics, Charité, Universitätsmedizin Berlin, Berlin, Germany. 3Human Molecular Genetics Laboratory, National Institute for Biotechnology & Genetic Engineering (NIBGE), Faisalabad, Pakistan. 4National Research Centre Frontiers in Genetics, Department of Zoology and Animal Biology, University of Geneva, Geneva, Switzerland. 5Berlin-Brandenburg Center for Regenerative Therapies (BCRT), Charité, Universitätsmedizin Berlin, Berlin, Germany. The molecular mechanisms that govern bone and joint formation are complex, involving an integrated network of signaling pathways and gene regulators. We investigated the role of Hox genes, which are known to specify individual segments of the skeleton, in the formation of autopod limb bones (i.e., the hands and feet) using the mouse mutant synpolydactyly homolog (spdh), which encodes a polyalanine expansion in Hoxd13. We found that no cortical bone was formed in the autopod in spdh/spdh mice; instead, these bones underwent trabecular ossification after birth. Spdh/spdh metacarpals acquired an ovoid shape and developed ectopic joints, indicating a loss of long bone characteristics and thus a transformation of metacarpals into carpal bones. The perichon- drium of spdh/spdh mice showed abnormal morphology and decreased expression of Runt-related transcription factor 2 (Runx2), which was identified as a direct Hoxd13 transcriptional target. Hoxd11–/–Hoxd12–/–Hoxd13–/– tri- ple-knockout mice and Hoxd13–/–Hoxa13+/– mice exhibited similar but less severe defects, suggesting that these Hox genes have similar and complementary functions and that the spdh allele acts as a dominant negative. -
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Cartilage Development and Maturation In Vitro and In Vivo Johnathan Ng Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Graduate School of Arts and Sciences Columbia University 2017 © 2017 Johnathan Ng All rights reserved Abstract Cartilage Development and Maturation In Vitro and In Vivo Johnathan Ng The articular cartilage has a limited capacity to regenerate. Cartilage lesions often result in degeneration, leading to osteoarthritis. Current treatments are mostly palliative and reparative, and fail to restore cartilage function in the long term due to the replacement of hyaline cartilage with fibrocartilage. Although a stem-cell based approach towards regenerating the articular cartilage is attractive, cartilage generated from human mesenchymal stem cells (hMSCs) often lack the function, organization and stability of the native cartilage. Thus, there is a need to develop effective methods to engineer physiologic cartilage tissues from hMSCs in vitro and assess their outcomes in vivo. This dissertation focused on three coordinated aims: establish a simple in vivo model for studying the maturation of osteochondral tissues by showing that subcutaneous implantation in a mouse recapitulates native endochondral ossification (Aim 1), (ii) develop a robust method for engineering physiologic cartilage discs from self-assembling hMSCs (Aim 2), and (iii) improve the organization and stability of cartilage discs by implementing spatiotemporal control during induction in vitro (Aim 3). First, the usefulness of subcutaneous implantation in mice for studying the development and maintenance of osteochondral tissues in vivo was determined. By studying juvenile bovine osteochondral tissues, similarities in the profiles of endochondral ossification between the native and ectopic processes were observed. -
Epiphyseal Photopenia Associated with Metaphyseal Osteomyelitis and Subperiosteal Abscess
Epiphyseal Photopenia Associated with Metaphyseal Osteomyelitis and Subperiosteal Abscess Patrice K. Rehm and John Delahay Division ofNuclear Medicine, Departments ofRadiology and Orthopedic Surgery, Georgetown University Hospital, Washington, DC fevers and knee pain necessitating surgical exploration. An abscess We present a case of metaphysealosteomyelitis in a child where was present, with a small amount of purulence within the bone, as bone scintigraphy demonstrated photopenia of the distal femoral well as copious purulent material beneaththe metaphysealperios epiphysis in the absence of infection of the epiphysis or the joint space. A subsequent bone scan demonstrated evolution of the teum medially, neither being under pressure. No effusion or vascular compromise of the epiphysis due to the metaphyseal purulence was found within the joint or the epiphysis. Copious osteomyelitis complicated by subperiosteal abscess. We discuss irrigation was performed and drains were left in place. Antibiotic the mechanisms and implications of photopenia in the setting of therapy was changed to intravenous penicillin. Gram stain and acute bone and joint infection. cultures of the purulent sitessubsequentlywere positive for Group Key Words epiphyseal photopenia; metaphyseal osteomyelitis; A strep and the epiphysis andjoint sites were negative. subperiostealabscess; bone scintigraphy Becauseof spikingfeversandcontinuedkneepain, the patient J Nuci Med 1998 391084-1086 underwent a second surgical exploration and debridement on the fifth hospital day. Purulent material was found within the knee joint and within the metaphysis, neither being under pressure. Photopeniaonbonescintigraphyintheclinicalsettingofacute The child defervesced and completed a 6-wk course of intrave bone and joint infection is well recognized. It may occur by a nous ceftriaxone. A three-phase bone scan 1 mo after onset variety of mechanisms, all related to alterations in blood flow revealed increased activity of the distal femoral epiphysis in and delivery ofthe radiotracer secondary to infection. -
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. -
Bones of the Skeletal System
BIOLOGY 211: HUMAN ANATOMY & PHYSIOLOGY ********************************************************************************************************* BONES OF THE SKELETAL SYSTEM ********************************************************************************************************** Reference: Saladin, KS: Anatomy & Physiology, The Unity of Form and Function, 6th ed. (2012) or 7th ed. (2015) Please review Chapters 7 & 8 before beginning this lab. INTRODUCTION The skeletal system has a number of important functions in the human body. It is the framework around which the body is organized, it provides levers for muscles to pull against, and it surrounds and protects many soft organs. Equally important, bones serve as a "buffer" in which calcium and other ions can be deposited and withdrawn according to the changing needs of the body, and they are the site of almost all blood cell production. Contrary to our popular conceptions, bones are not rigid, inflexible structures: they are constantly changing, and can have a remarkable degree of flexibility before they break. The organs of the skeletal system are the bones and joints, and like all organs are composed of different types of tissue. Although we tend to classify them into "types" such as "long bones", "flat bones", etc., each is in fact unique and ideally suited to its particular location and function. We classify bones as belonging to either: a) the axial skeleton (head and trunk) b) the appendicular skeleton (arms and legs), However, you should always bear in mind that the entire skeletal system functions as a unit. If you look at any bone, you will see that it is rarely flat or smooth. Bones have a variety of bumps, grooves, holes, etc. which allow them to serve their specific functions.