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Cartilage. Biomedical Aspects PDF

354 Pages·1983·8.186 MB·English
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CONTRIBUTORS James A. Albright William A. Beresford M. Michael Cohen, Jr. Michael W. Elves Paul F. Goetinck Richard J. Goss Brian K. Hall C. W. McCutchen R. P. Misra Leon Sokoloff Bruce A. Wright Cartilage V O L U ME 3 Biomédical Aspects Edited by BRIAN K. HALL Department of Biology Dalhousie University Halifax, Nova Scotia Canada 1983 ACADEMIC PRESS A Subsidiary of Harcourt Brace Jovanovich, Publishers New York London Paris San Diego San Francisco Säo Paulo Sydney Tokyo Toronto COPYRIGHT © 1983, BY ACADEMIC PRESS, INC. ALL RIGHTS RESERVED. NO PART OF THIS PUBLICATION MAY BE REPRODUCED OR TRANSMITTED IN ANY FORM OR BY ANY MEANS, ELECTRONIC OR MECHANICAL, INCLUDING PHOTOCOPY, RECORDING, OR ANY INFORMATION STORAGE AND RETRIEVAL SYSTEM, WITHOUT PERMISSION IN WRITING FROM THE PUBLISHER. ACADEMIC PRESS, INC. Ill Fifth Avenue, New York, New York 10003 United Kingdom Edition published by ACADEMIC PRESS, INC. (LONDON) LTD. 24/28 Oval Road, London NW1 7DX Library of Congress Cataloging in Publication Data Main entry under title: Cart iläge. Includes bibliographical references and index. Contents: v. 1. Structure, function, and biochemistry- v. 3- Biomédical aspects. 1. Cartilage. I. Hall, Brian Keith, Date QP88.2.C37 1982 59ΚΓ852 82-20566 ISBN O-I2-319503-9 (v. 3) PRINTED IN THE UNITED STATES OF AMERICA 83 84 85 86 9 8 7 6 5 4 3 2 1 Contributors Numbers in parentheses indicate the pages on which the authors' contributions begin. James A. Albright (49), Department of Orthopaedic Surgery, School of Medicine, Louisiana State University Medical Center, Shreveport, Louisiana 71103 William A. Beresford (1), Department of Anatomy, West Virginia University, Morgantown, West Virginia 26506 M. Michael Cohen, Jr. (143, 191), Faculties of Dentistry and Medicine, Dalhousie University, Halifax, Nova Scotia B3H 4J1, Canada Michael W. Elves (229), Glaxo Group Research Ltd., Greenford, Middlesex UB6 OHE, England Paul F. Goetinck (165), Department of Animal Genetics, and Genetics and Cell Biology Section of the Biological Sciences Group, The University of Connecticut, Storrs, Connecticut 06268 Richard J. Goss (267), Division of Biology and Medicine, Brown University, Providence, Rhode Island 02912 Brian K. Hall (309), Department of Biology, Dalhousie University, Halifax, Nova Scotia B3H 4J1, Canada C. W. McCutchen (87), National Institutes of Health, Bethesda, Maryland 20205 R. P. Misra (49), Department of Pathology, School of Medicine, Louisiana State University Medical Center, Shreveport, Louisiana 71103 Leon Sokolojf (109), Department of Pathology, State University of New York at Stony Brook, Stony Brook, New York 11794 Bruce A. Wright (143), Faculty of Dentistry, Dalhousie University, Halifax, Nova Scotia B3H 4J1, Canada IX Preface This is the third in a series of three volumes devoted to cartilage. Volume 1 dealt with the structure, function, and biochemistry of cartilage; Volume 2 dealt with cartilage's development, differentiation, and growth. This volume covers what I have termed the biomédical aspects of cartilage. Although the topics covered in Volumes 1 and 2 all impinge on the study of cartilage in the human body, the chapters in this volume are more directly related to the inevitable deterioration of cartilage that accompanies aging, disease, or genetic mutations. The introductory chapter discusses the formation of cartilage outside the confines of the skeleton—the so-called ectopic cartilages. It highlights the important but little understood neoplastic and metaplastic processes that produce ectopic cartilage. For a comprehensive overview of mechanisms of cartilage differentiation, this chapter should be read in conjunction with the opening chapter in Volume 2. Several chapters highlight aspects of age-related changes in cartilage: résorp- tion and remodeling in Chapter 2, lubrication in Chapter 3, and degenerative diseases in Chapter 4. These chapters summarize current theories of how carti- lage is maintained under conditions that would be expected to lead to perpetual remodeling, résorption, and functional diminution. Cartilage normally resists invasion by tumors; this is discussed in Volume 1, Chapter 11. Chapter 5 dis- cusses those tumors that do manage to invade cartilage. Two chapters then deal with mutations that affect cartilage. Chapter 6 concentrates on those affecting limb cartilages and highlights the molecular and biochemical bases of some well-studied mutations. Chapter 7 concentrates on mutations that affect cranio- facial cartilages and that lead to craniofacial anomalies and growth deficiencies. Here the emphasis is more clinical. Taken together, these two chapters provide a balanced overview of those mutations that affect cartilage and how they might act. Immunological properties of cartilage, both in situ and when used as a graft to stimulate repair, are extensively discussed in Chapter 8, a chapter that empha- sizes the need for combined basic and clinical approaches to this important topic. Chapter 9 provides an overview of the role of cartilage in situations involving regeneration and repair of skeletal tissues, and Chapter 10 discusses bioelectrical properties of cartilage and the response of cartilage to bioelectrical stimulation, both in vivo and in vitro. xi Xll Preface Once again it is a pleasure to thank all of the contributors for their willingness to take time from very busy schedules to review their specialized fields within the framework of biomédical aspects of cartilage. It is my hope that this volume, and indeed the three volumes, will serve to emphasize the need for collaborative and coordinated basic and clinical research on cartilage while summarizing current knowledge and pointing toward approaches for the future. Although much has already been done, much remains to be done. CONTENTS OF OTHER VOLUMES Volume 1: Structure, Function, and Biochemistry 1. Vertebrate Cartilages 7. Collagens of Cartilage Melvin L. Moss and Letty Moss-Salentijn Richard Mayne and Klaus von der Mark 2. Invertebrate Cartilages 8. Glycosaminoglycans of Cartilage Philip Person James W. Lash and N. S. Vasan 9. Metabolism of Cartilage 3. The Chondroblast and the Chondrocyte R. A. Stockwell Robert A. Kosher 10. Vascularity of Cartilage 4. Transmission Electron Microscopy of Klaus E. Kuettner and Bendicht U. Cartilage Pauli Huntington Sheldon 11. Biomechanics of Cartilage and Its 5. Scanning Electron Microscopy of Response to Biomechanical Stimuli Cartilage Elizabeth R. Myers and Van C. Mow Alan Boy de and Sheila J. Jones 12. Calcification of Cartilage 6. Cell Kinetics of Cartilage S. YousufAli N. F. Kember Index Volume 2: Development, Differentiation, and Growth 1. The Origin of Cartilage: Investigations in 6. Morphogenesis of Cartilage Quest of Chondrogenic DNA Peter Thorogood Marshall R. Urist 7. Growth of Cartilage 2. Control of Cartilage Differentiation J. R. Hinchliffe and D. R. Johnson Susan J. Hunter and Arnold I. Caplan 3. Cell-Cell Interactions and 8. Vitamins and Cartilage Chondrogenesis Asher Ornoy and Igor Zusman Michael Solursh 9. Hormones and Cartilage 4. Cellular Condensations and Michael Silbermann Chondrogenesis 10. Growth Factors and Cartilage D. A. Ede William A. Elmer 5. Tissue Interactions and Chondrogenesis Brian K. Hall Index Xlll I Ectopic Cartilage, Neoplasia, and Metaplasia William A. Beresford I. Introduction 1 II. Extraskeletal versus Ectopic Cartilage 2 III. Specious Ectopic Cartilages 4 IV. Tumors and Tumor-Like Conditions with Ectopic Cartilage 5 A. Osseous Tumors 8 B. Benign ExtraosseousTumors 8 C. Malignant Extraosseous Tumors 11 D. Composite Extraosseous Tumors 14 E. Miscellaneous Extraosseous Tumors 19 F. Tumor-Like Conditions 20 G. Cartilage in Malformations 23 H. Veterinary Examples of Ectopic Cartilage 24 V. Experimental Ectopic Cartilage 24 A. Embryonic Cartilage 24 B. Extraosseous Cartilage in "Maturity" 26 VI. Discussion and Summary 31 A. Matrix Synthesis and Variety 31 B. Precursor Cells 31 C. Stimuli 33 References 34 I. INTRODUCTION To pronounce a tissue of an individual as out of its rightful place requires a thorough knowledge of anatomy and its variations. Thus, cartilage is ex- pected in the tongue of a dog, but not in that of a human. Cartilages occur- ring separately from the principal skeleton, ear, and airway, and as a normal part in a particular species, will here be called extraskeletal, in distinction to ectopic (EC) cartilage, which is not usually found at the site in any member of that species. This convention is necessary here, but contradicts (7) the common practice of clinicians to use extraskeletal in the sense of ectopic and (2) the skeletal role of the extraskeletal cartilages in the heart, tongue, eye, and elsewhere. Cartilage also arises on or within the skeleton and will be named osseous ectopic. For the EC cartilage of soft tissues, extraosseous will 1 Cartilage, Volume 3 Copyright © 1983 by Academic Press, Inc. Biomédical Aspects All rights of reproduction in any form reserved. ISBN 0-12-319503-9 2 William A. Beresford be used. Difficulties and points of interest between the extraskeletal and ec- topic categories will be explored. How easy is it to claim a material in a soft-tissue or bony site as cartilage? Chondroid, pseudocartilage, myxoid, chondroosteoid, and other entities have been hard to distinguish from cartilage, and in some instances the terms may have been misnomers for proper cartilage (see Volume 1, Chapters 1 and 2). True cartilage, of course, has a wide range of forms. How well the ec- topic instances meet the morphological and histochemical criteria for car- tilage, and the better criteria becoming available will be discussed. Most EC cartilage falls into Schaffer's (1930) class of secondary cartilage, appearing after the establishment of the primary cartilaginous skeleton, and frequently much later in life. The formation of EC cartilage in an already formed and functioning soft connective tissue implies the conversion of one differentiated tissue into another, that is, a metaplasia (Virchow, 1884; Willis, 1962). Metaplasia might also happen, were EC cartilage to experience a direct conversion to bone, as is sometimes claimed. In its unexpected late development, the cartilage is a new growth, but when it is normal cartilage, limited in its growth, it is scarcely a neoplasm. However, many cartilage- bearing soft-tissue lesions are without question neoplastic in the modern sense. Consideration will be given to the fit of the concepts of metaplasia and neoplasia to pathological and experimental EC cartilage. II. EXTRASKELETAL VERSUS ECTOPIC CARTILAGE Schaf fer (1930), Willis (1962), and Beresford (1981) list the many sites of ex- traskeletal cartilage in various species. Examples are still cofning to light, thus the fibrocartilaginous reinforcements in the urethral process of the goat's penis (Ghoshal and Bal, 1976) and the submandibular ventral pouch of rorqual whales (Pivorunas, 1977). The latter cartilage is closely bound to the mylohyoid muscle. A similarly intimate relation to muscle exists for a previously undescribed anterior element of the hyoid skeleton of the finch, Passer: the preglossale (Bock and Morony, 1978). This forms late via car- tilage, articulates with another bone, and is definitely skeletal. The interest in the preglossale with regard to EC cartilage lies in its absence in all other birds and their possible reptilian ancestors, making it a skeletal neomorph. Bock and Morony suggest that it might have originated phylogenetically as an ectopic splint for its muscle, which developed a joint with the paraglossale and somehow became a constant skeletal element. This hypothesis of a skeletal element being a genetically incorporated manifestation of an earlier EC cartilage contrasts with the more common, but ill-founded, view of EC mammalian abdominal-wound and scierai car- 1. Ectopic Cartilage, Neoplasia, and Metaplasia 3 tilages as atavistic expressions of crocodilian abdominal ribs and reptilian scierai cartilage. But atavism cannot be cast out altogether. The human os paracuneiforme, accessory to the tarsus, presumably forms in a cartilage, which by its sporadic presence might (but should not) be considered ectopic. Conroy (1978) argues that this element is the vestigial homolog of the primate prehallux. Returning to the hyoid apparatus, Gentscheff (1934) saw small islands of hyaline cartilage in around 30% of human tongues (including those of newborns) near the tip where the genioglossal muscle inserts into the septum. The position of the cartilage matches that of the carnivores' lyssa, which led Gentscheff to conclude that both instances constitute a relic of the rod in ancestral reptilian tongues. This inconstant extraskeletal cartilage has not confused the categorization of other lingual nodules in man as ectopic (see Section IV,B,1), because its existence is virtually unknown, and the chon- dromas are off the midline and not so anterior. Misconceptions have arisen because of ignorance of the partly car- tilaginous nature of the cardiac skeleton in many species (Benninghoff, 1930). For dog and human, clinical reports of EC cartilage (James and Drake, 1968; Ferris and Aherne, 1971) ignored fibrocartilage as a normal component of these hearts (Balogh, 1971; Sandusky et ai, 1979). The hyaline cartilage in the aortic ring of the rat, although not thought to be ec- topic, was construed as an aspect of cardiac aging, until Hollander (1968) showed its presence from the second week of life. On the other hand, truly EC cartilage develops in healing infarcts in the rat's ventricular wall and in the diseased human aortic valve. The inconstant occurrence of certain cartilage bones might seem to blur the distinction between EC and extraskeletal cartilages, but rarity is not ec- topia. The number and form of sesamoids in the hands and feet show how great the anatomical variation can be (Jacobs, 1974; Scranton and Rutkow- ski, 1980). When the frequency of the accessory bone drops very low, calling it and its cartilaginous precursor extraskeletal recognizes a weak genetic commitment to chondrogenesis at that site that the term ectopic denies. Constraints are transmitted to an offspring along with the genetic endow- ment to cells of the ability to respond to proliferative and other stimuli. Ec- topic chondrogenesis reflects the persistent responsiveness of fibroblasts and perhaps other cells, and the slackening of controls hitherto keeping them fibroblastic. Extraskeletal cartilages occupy consistent positions because of the constraints. Beyond this simple view is the complex interplay between genome, cells, tissues, and stimuli in the individual and over generations, resulting in the variable presence of some bones and cartilages, the forma- tion of EC cartilage in response to stimuli that are ineffective in other in-

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