DOCSLIB.ORG

Cartilage and Bone Connective Tissue

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Cartilage and Bone Connective Tissue Chapter 6 Cartilage and Bone Connective Tissue Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Review Chapter 4 – Tissues connective tissues Skeletal System Components Functions (mostly of bone) • bones • support • protection • cartilage • lever for movement • ligaments • major storage and source of ++ --- • other – minerals: Ca and PO4 as calcium supportive phosphate & calcium carbonate connective – fat in white marrow: lipid-soluble hormones & vitamins tissue • hematopoiesis: blood cell formation & structures maturation in spongy bone spaces Skeletal System • cartilage “semi-rigid” • bone • chondrocytes • osteocytes • avascular – osseous tissue – hyaline cartilage • ~ 2/3 mineral = mostly • basic cartilage structure hydroxylapatite = calcium phosphate + • mostly ground substance calcium carbonate • few & thin fibers • ~ 1/3 collagen fibers – usually not visible • + cells = osteocytes – fibrocartilage • ~ hyaline cartilage + – compact bone collagen fiber bundles • osteons – elastic cartilage – spongy bone • ~ hyaline cartilage + elastic • trabecula(e) fiber bundles cartilage in the skeletal system Figure 6.1 hyaline “glassy” cartilage - translucent perichondrium perichondrium perichondrium fibrocartilage: resilient, shock absorber NO perichondrium blends with surrounding DIFCT elastic cartilage: flexible yes perichondrium --- not shown here Formation Figure 6.2 and Growth of Cartilage chondroblast chondrocyte perichondrium lacuna appositional vs interstitial growth Formation and Growth of Cartilage ORIGIN = mesenchyme: cluster of mesenchymal cells Central cells become chondrocytes; outer rim → perichondrium with chondroblasts appositional growth interstitial growth “appose” – at edge, nearby “between the stuff” • mitosis of stem cells in • mitosis of chondrocytes in lacunae perichondrium • → two chondroblasts per lacuna • adds chondroblasts to periphery • each synthesize and secrete new • → produce matrix, matrix • become chondrocytes in lacunae • new matrix separates the cells, • results: now called chondrocytes – larger piece of cartilage • results: – newest cartilage on outside – larger piece of cartilage edges – newest cartilage on the inside 5 bone shape categories ALL: compact bone on outside & spongy bone in center • long • cuboidal – not so“short” • flat • irregular • odd (also part of other shape group) – sutural = Wormian – sesamoid not all so “short” !!→ Figure 6.3 cells in bone – note effects on bone & on serum (blood) Ca++ stem cells Figure 6.6 cells in bone – note their effects on bone & on serum (blood) Ca++ • Osteoprogenitor cells – stem cells from mesenchyme – found in endosteum and periosteum → either another stem cell or an osteoblast • Osteoblasts – >> bone matrix – differentiates into osteocytes • Osteocytes – in lacunae – maintain the bone matrix – communicate with osteoblasts →deposit more bone matrix • Osteoclasts – large, multinuclear cells <– derived from fused macrophages – in resorption lacunae – dissolve bone = osteolysis → releases Ca++ • Osteoclasts and osteoblasts have opposite effects on bone density & serum Ca++ bone matrix composition • organic and inorganic components – ~ 1/3 organic • cells • collagen fibers • ground substance – ~ 2/3 inorganic • Ca++ salts – Calcium hydroxide – calcium phosphate →bone salt crystals = hydroxyapatite – Ca10(PO4)6(OH)2 ** but actually quite variable *** Table 6.1 Page 153_01 Osteitis deformans imbalance between osteoclast & osteoblast activities Figure 6.5 periosteum & endosteum osteoblasts red marrow fused macrophages Figure 6.8 compact bone tissue: osteons & spongy bone tissue • central (Haversian) canal – carries vessels and nerves in center of osteon • concentric lamellae “lamella” = “layer” – rings of bone around central canal • osteocytes in lacunae between lamellae • canaliculi = channels between lacunae – osteocytes connect & communicate – nutrient & waste exchange < -- > central canal • circumferential lamellae – rings of bone immediately internal to • periosteum • endosteum – entire circumference of the bone • interstitial lamellae Compact Bone – leftover parts of osteons that have Microscopic been partially resorbed Anatomy bone is dynamic – remodeling constantly Click to edit Master title style • osteon (Haversian system) Compact Bone - – basic unit of compact bone – cylindrical Osteons – parallel to the diaphysis • Parallel to compression stress lines • perforating canals – ~ perpendicular to & connect multiple central canals – passageways for blood & lymphatic vessels and nerves • rings of lacunae between lamellae • canaliculi – allow osteocytes to interact What else do you see? Figure 6.9 scanning EM LM: H & E spongy bone NO osteons why not? • immersed in red marrow • no need for central canals • lamellae • lacunae • canaliculi • endosteum • osteoclasts why ? What else do you see? How do the osteocytes survive? Figure 6.7 Figure 6.4 Long Bone • 1 diaphysis – mostly compact bone – marrow cavity • 2 epiphyses – mostly spongy bone • 2 metaphyses Bone Structure – not just long bones • Articular cartilage – Hyaline cartilage – Covers articulating surfaces of any bone participating in a synovial joint • No pericondrium against bone • Endosteum covers – Internal surface – Trabeculae • Periosteum – DIFCT / DRFCT depending on mechanical stress at site – Perforating fibers anchor into compact bone Long Bone Structure • red marrow – found in all spongy bone – hematopoiesis • yellow marrow – in medullary cavity of [large] long bones – adipose tissue – store lipid soluble • hormones • vitamins OSSIFICATION – OSTEOGENESIS ~ 8th week prenatal → entire life ENCHONDRAL O.- INTRAMEMBRANOUS O.- • hyaline cartilage • mesenchyme model • skull flat bones • most bones (most) • (– see exceptions →) • some facial bones • mandible • central clavicle intramembranous ossification • mesenchymal cells form fibrous CT • some differentiate into osteoblasts • → lay down osteoid • → calcification • enclosed cells differentiate into woven bone osteocytes • Note: bone is never exposed – there is ALWAYS a periosteum lamellar bone of DFCT Figure 6.10 enchondral ossification – e.g. long bone Figure 6.11 Stages of Endochondral Ossification • fetal hyaline cartilage model develops • cartilage calcifies due to invasion by blood vessels and increased oxygen • periosteal bone collar forms • primary ossification center forms in the diaphysis • secondary ossification centers form in the epiphyses • bone replaces cartilage, except – articular cartilage – epiphyseal plates • epiphyseal plates ossify and form epiphyseal lines hormonal effects ~ puberty & beyond Page 159_01 15 – 23 years old < 15 years old note extent of epiphyseal fusion Epiphyseal Plate Zones Figure 6.13 “appositional” bone growth – growth in diameter or thickness – requires remodeling – osteoclast activity – osteoblast activity arterial supply to a long bone * all bones * ** Nutrient arteries and veins • supply the diaphysis of long bones • nerves usually accompany these blood vessels into the bone Metaphyseal arteries and veins • supply the junctional area between the diaphysis and the epiphysis Epiphyseal arteries and veins • supply the cells of the Figure 6.14 epiphyseal plate ** Periosteal arteries and veins • supply blood to the external circumferential lamellae • superficial osteons Page 163_01 Bone scans measure metabolic activity • “hot spot” = increased metabolism • “cold spot” = decreased metabolism Homeostasis & Promoting Bone Growth growth, maintenance, and repair depend on: • hormones: regulate osteoblast and osteoclast activity → regulate calcium levels • growth hormone stimulates cartilage growth at epiphyseal plate • thyroid hormone stimulates metabolic rate of osteoblasts • calcitonin and parathyroid hormone have opposite effects on calcium • calcitonin promotes calcium deposit from blood to bone • parathyroid hormone stimulates osteoclasts to resorb bone and increase levels of calcium in the blood • vitamins • vitamin A activates osteoblasts • vitamin C required for collagen synthesis • vitamin D stimulates calcium absorption from GI tract into blood • so that calcium is available for building bone • Exercise • mechanical stress stimulates increase in bone density by increased osteoblast activity • bones of athletes become thicker and stronger as the result of repetitive and stressful exercise • bones lose mass with age, but this can be slowed or reversed with weight-bearing exercise Homeostasis & Promoting Bone Growth Figure 6.15 Bone Fractures Table 6.2 Bone Fractures Figure 6.15 Bone Fractures Figure 6.15 Figure 6.16 Bone Fracture Repair (usually 4-8 weeks if all goes well) Figure 6.17 Bone Markings & Landmarks bone -- ageing during aging, bone changes in two main ways: • loses ability to produce organic matrix (mainly collagen) • loses calcium and other minerals – osteopenia: insufficient ossification – can result in a decrease in bone mass called osteoporosis – increase chances of fractures • Note – the ability to repair & remodel is maintained – though possibly impaired Page 167_01 Osteogenesis –> Osteoporesis - animation.
Load more

Recommended publications
  • Mesenchymal Stem Cells in Combination with Hyaluronic Acid
    www.nature.com/scientificreports OPEN Mesenchymal Stem Cells in Combination with Hyaluronic Acid for Articular Cartilage Defects Received: 1 August 2017 Lang Li1, Xin Duan1, Zhaoxin Fan2, Long Chen1,3, Fei Xing1, Zhao Xu4, Qiang Chen2,5 & Accepted: 19 April 2018 Zhou Xiang1 Published: xx xx xxxx Mesenchymal stem cells (MSCs) and hyaluronic acid (HA) have been found in previous studies to have great potential for medical use. This study aimed to investigate the therapeutic efects of bone marrow mesenchymal stem cells (BMSCs) combined with HA on articular cartilage repair in canines. Twenty-four healthy canines (48 knee-joints), male or female with weight ranging from 5 to 6 kg, were operated on to induce cartilage defect model and divided into 3 groups randomly which received diferent treatments: BMSCs plus HA (BMSCs-HA), HA alone, and saline. Twenty-eight weeks after treatment, all canines were sacrifced and analyzed by gross appearance, magnetic resonance imaging (MRI), hematoxylin-eosin (HE) staining, Masson staining, toluidine blue staining, type II collagen immunohistochemistry, gross grading scale and histological scores. MSCs plus HA regenerated more cartilage-like tissue than did HA alone or saline. According to the macroscopic evaluation and histological assessment score, treatment with MSCs plus HA also lead to signifcant improvement in cartilage defects compared to those in the other 2 treatment groups (P < 0.05). These fndings suggested that allogeneic BMSCs plus HA rather than HA alone was efective in promoting the formation of cartilage-like tissue for repairing cartilage defect in canines. Articular cartilage is composed of chondrocyte and extracellular matrix and has an important role in joint move- ment including lubrication, shock absorption and conduction.
    [Show full text]
  • (AMIC) Compared to Microfractures for Chondral Defects of the Talar Shoulder: a Five-Year Follow-Up Prospective Cohort Study
    life Communication Autologous Matrix Induced Chondrogenesis (AMIC) Compared to Microfractures for Chondral Defects of the Talar Shoulder: A Five-Year Follow-Up Prospective Cohort Study Filippo Migliorini 1 , Jörg Eschweiler 1, Nicola Maffulli 2,3,4,5,* , Hanno Schenker 1, Arne Driessen 1 , Björn Rath 1,6 and Markus Tingart 1 1 Department of Orthopedics and Trauma Surgery, University Clinic Aachen, RWTH Aachen University Clinic, 52064 Aachen, Germany; [email protected] (F.M.); [email protected] (J.E.); [email protected] (H.S.); [email protected] (A.D.); [email protected] (B.R.); [email protected] (M.T.) 2 School of Pharmacy and Bioengineering, Keele University School of Medicine, Staffordshire ST4 7QB, UK 3 Barts and the London School of Medicine and Dentistry, London E1 2AD, UK 4 Centre for Sports and Exercise Medicine, Queen Mary University of London, Mile End Hospital, London E1 4DG, UK 5 Department of Orthopedics, Klinikum Wels-Grieskirchen, A-4600 Wels, Austria 6 Department of Medicine, Surgery and Dentistry, University of Salerno, 84081 Baronissi, Italy * Correspondence: [email protected] Abstract: Introduction: Many procedures are available to manage cartilage defects of the talus, Citation: Migliorini, F.; Eschweiler, J.; including microfracturing (MFx) and Autologous Matrix Induced Chondrogenesis (AMIC). Whether Maffulli, N.; Schenker, H.; Driessen, AMIC or MFx are equivalent for borderline sized defects of the talar shoulder is unclear. Thus, the A.; Rath, B.; Tingart, M. Autologous present study compared the efficacy of primary isolated AMIC versus MFx for borderline sized Matrix Induced Chondrogenesis focal unipolar chondral defects of the talar shoulder at midterm follow-up.
    [Show full text]
  • Applications of Chondrocyte-Based Cartilage Engineering: an Overview
    Hindawi Publishing Corporation BioMed Research International Volume 2016, Article ID 1879837, 17 pages http://dx.doi.org/10.1155/2016/1879837 Review Article Applications of Chondrocyte-Based Cartilage Engineering: An Overview Abdul-Rehman Phull,1 Seong-Hui Eo,1 Qamar Abbas,1 Madiha Ahmed,2 and Song Ja Kim1 1 Department of Biological Sciences, College of Natural Sciences, Kongju National University, Gongjudaehakro 56, Gongju 32588, Republic of Korea 2Department of Pharmacy, Quaid-i-Azam University, Islamabad 45320, Pakistan Correspondence should be addressed to Song Ja Kim; [email protected] Received 14 May 2016; Revised 24 June 2016; Accepted 26 June 2016 Academic Editor: Magali Cucchiarini Copyright © 2016 Abdul-Rehman Phull et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Chondrocytes are the exclusive cells residing in cartilage and maintain the functionality of cartilage tissue. Series of biocomponents such as different growth factors, cytokines, and transcriptional factors regulate the mesenchymal stem cells (MSCs) differentiation to chondrocytes. The number of chondrocytes and dedifferentiation are the key limitations in subsequent clinical application of the chondrocytes. Different culture methods are being developed to overcome such issues. Using tissue engineering and cell based approaches, chondrocytes offer prominent therapeutic option specifically in orthopedics for cartilage repair and to treat ailments such as tracheal defects, facial reconstruction, and urinary incontinence. Matrix-assisted autologous chondrocyte transplantation/implantation is an improved version of traditional autologous chondrocyte transplantation (ACT) method. An increasing number of studies show the clinical significance of this technique for the chondral lesions treatment.
    [Show full text]
  • Embryonic Cell That Forms Cartilage Medical Term
    Embryonic Cell That Forms Cartilage Medical Term Unexploited Gordie languishes: he scumbles his initiatives atweel and esthetically. When Nate gestate his niggardliness Grecizing not post-free enough, is Mikhail windowless? Ship-rigged or millionth, Edgar never enshrining any millionairesses! The crest cell phenotype research in record area forms the body of shift review the Table 1. Where and repair differs substantially augments the embryonic cartilage tissue types of its tension adaptation and cells? In both types for medicine to that cartilage. Cells turn into differentiated stem cells that trace specific tissues and organs. Ambiguous cells the emergence of daughter stem a concept in. Mesenchymal Chondrosarcoma NORD National. Blood cells Chondro Oma Cartilage Tumor Arthro Joints Cartilage creates a. Can disturb blood cells and stromal which manufacture produce fat cartilage and bone. Label by following from NURSING 3345 at University of Texas Medical Branch. Body mostly a laboratory stem cells divide that form more cells called daughter cells. Guidelines for Human Embryonic Stem Cell with Brown. Abstract The skeletal system is formed of bones and cartilage which are. Each tissue cartilage bone and skeletal muscle goes through my different. Medical terms UCL. Please note love the definitions are moving given an explain another word found also a. Definition Stem cells are cells which feature not yet developed a special. The term totipotent refer down the grief that they ever total potential to. Stem from Research Uses Types & Examples Healthline. For cardiac muscle cells and was still pluripotent stem cells may also structures and cartilage that embryonic cell forms a primitive connective tissue physiology as well as macrophages are adequately informed consent.
    [Show full text]
  • Research Review Fibrocartilage
    J. Anat. (1990), 171, pp. 1-15 1 Printed in Great Britain Research Review Fibrocartilage M. BENJAMIN AND E. J. EVANS Department of Anatomy, University of Wales College of Cardiff, PO Box 900, Cardif CF1 3 YF, Wales Fibrocartilage has long been a neglected tissue that is too often viewed as a poor relation of hyaline cartilage. It failed to achieve the status of a tissue with the early histologists, but it is beginning to come of age, for modem techniques are revealing some exciting secrets about fibrocartilage in knee joint menisci and intervertebral discs in particular. Yet there has never been any general review on fibrocartilage, and workers concerned with the tissue in one organ rarely consider it in another. Consequently, we lack any global picture that would encourage the spread of interest in the tissue and the effective exchange of ideas. Our review deals largely with the white fibrocartilage of standard texts and for reasons of space excludes yellow elastic cartilage. We have concentrated on fibrocartilage as a tissue rather than fibrocartilages as organs. HISTORICAL CONSIDERATIONS The most important work on cartilage in the older literature is that of Schaffer (1930). His monograph is a thorough, comparative account of cartilage and related tissues throughout the animal kingdom. The reader interested in fibrocartilage must also study Schaffer's account of chondroid tissue, for some tissues that would now be regarded as fibrocartilage were viewed by Schaffer as hyaline-cell chondroid tissue. He had a narrow vision of 'true' cartilage and called tissues where the cells were not shrunken in lacunae, 'chondroid'.
    [Show full text]
  • Comparative Anatomy of the Lower Respiratory Tract of the Gray Short-Tailed Opossum (Monodelphis Domestica) and North American Opossum (Didelphis Virginiana)
    University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Doctoral Dissertations Graduate School 12-2001 Comparative Anatomy of the Lower Respiratory Tract of the Gray Short-tailed Opossum (Monodelphis domestica) and North American Opossum (Didelphis virginiana) Lee Anne Cope University of Tennessee - Knoxville Follow this and additional works at: https://trace.tennessee.edu/utk_graddiss Part of the Animal Sciences Commons Recommended Citation Cope, Lee Anne, "Comparative Anatomy of the Lower Respiratory Tract of the Gray Short-tailed Opossum (Monodelphis domestica) and North American Opossum (Didelphis virginiana). " PhD diss., University of Tennessee, 2001. https://trace.tennessee.edu/utk_graddiss/2046 This Dissertation is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a dissertation written by Lee Anne Cope entitled "Comparative Anatomy of the Lower Respiratory Tract of the Gray Short-tailed Opossum (Monodelphis domestica) and North American Opossum (Didelphis virginiana)." I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Doctor of Philosophy, with a major in Animal Science. Robert W. Henry, Major Professor We have read this dissertation and recommend its acceptance: Dr. R.B. Reed, Dr. C. Mendis-Handagama, Dr. J. Schumacher, Dr. S.E. Orosz Accepted for the Council: Carolyn R.
    [Show full text]
  • Autologous Matrix-Induced Chondrogenesis and Generational Development of Autologous Chondrocyte Implantation
    Autologous Matrix-Induced Chondrogenesis and Generational Development of Autologous Chondrocyte Implantation Hajo Thermann, MD, PhD,* Christoph Becher, MD,† Francesca Vannini, MD, PhD,‡ and Sandro Giannini, MD‡ The treatment of osteochondral defects of the talus is still controversial. Matrix-guided treatment options for covering of the defect with a scaffold have gained increasing popularity. Cellular-based autologous chondrocyte implantation (ACI) has undergone a generational development overcoming the surgical drawbacks related to the use of the periosteal flap over time. As ACI is associated with high costs and limited in availability, autologous matrix-induced chondrogenesis, a single-step procedure combining microfracturing of the subchondral bone to release bone marrow mesenchymal stem cells in combination with the coverage of an acellular matrix, has gained increasing popularity. The purposes of this report are to present the arthroscopic approach of the matrix-guided autologous matrix-induced chondrogenesis technique and generational development of ACI in the treatment of chondral and osteochon- dral defects of the talus. Oper Tech Orthop 24:210-215 C 2014 Elsevier Inc. All rights reserved. KEYWORDS cartilage, defect, ankle, talus, AMIC, ACI Introduction Cartilage repair may be obtained by cartilage replacement: (OATS, mosaicplasty) or with techniques aimed to generate a hondral and osteochondral lesions are defects of the newly formed cartilage such as microfracture or autologous Ccartilaginous surface and underlying subchondral bone of chondrocyte implantation (ACI).9-17 the talar dome. These defects are often caused by a single or Arthroscopic debridement and bone marrow stimulation multiple traumatic events, mostly inversion or eversion ankle using the microfracture technique has proven to be an 1,2 sprains in young, active patients.
    [Show full text]
  • 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.
    [Show full text]
  • Adipose Derived Mesenchymal Stem Cell Differentiation Into Adipogenic and Osteogenic Stem Cells
    vv ISSN: 2641-3000 DOI: https://dx.doi.org/10.17352/sscrt LIFE SCIENCES GROUP Hassan IH El Sayyad1*, Mohamed A Sobh2, Soad A Khalifa1 and Omnia KR Research Article 3 El-Sayyad Adipose Derived Mesenchymal Stem 1Zoology Department, Faculty of Science, Egypt 2Urology & Nephrology Center, Research Center, Egypt Cell Differentiation into Adipogenic 3Pediatric Mansoura University Hospital, Mansoura University, Egypt and Osteogenic Stem Cells Dates: Received: 08 December, 2016; Accepted: 23 December, 2016; Published: 29 December, 2016 *Corresponding author: Hassan IH El-Sayyad, Depart- Abstract ment of Zoology, Faculty of Science, Mansoura University, Mansoura, Egypt, Tel: 0020502254850; Objective: Lipoaspiration of human breast fats are important source of adipocyte stem cells E-mail: (hAMSCs) which play a great role in regenerative medicine. The present study illustrates its capability of its transformation and characterization of adipocyte, osteogenic or chondrogenic cells. https://www.peertechz.com Methods and results: The hAMSCs were positive for CD13, CD29, CD105 and CD90 and negative CD34 and CD 14. The hAMSCs were cultured in adipogenic or osteogenic culture for 4,7,14 & 21 days. Gene expression for adipogenic (PCR of leptin, peroxisome proliferator-activated receptor-γ and lipoprotein lipase) and osteogenic (osteocalcin) cells were carried out. Biochemical assessments of adipogenic (lipoprotein lipase enzyme and glycerol-3-phosphate dehydrogenase) and osteogenic (alkaline phosphatase, B-galactosidase and calcium content) markers. Also, light and transmission electron microscopic investigation of adipocyte stem cell culture were investigated at 4,7,14 & 21 days in both two models. Adipocyte derived from hAMSCs displayed fi broblastic morphology and confl uency at 7 days and fl at-shape with positive oil red staining at 14 &21 days.
    [Show full text]
  • Connectomics of the Lacuno-Canalicular Network in Bone
    The Small World of Osteocytes: Connectomics of the Lacuno-Canalicular Network in Bone Philip Kollmannsberger1,2,*, Michael Kerschnitzki1,3, Felix Repp1, Wolfgang Wagermaier1, Richard Weinkamer1, Peter Fratzl1 1Max Planck Institute of Colloids and Interfaces, Department of Biomaterials, Potsdam, Germany 2ETH Zurich, Laboratory of Applied Mechanobiology, Department of Health Sciences and Technology, Zurich, Switzerland 3Weizmann Institute of Science, Dept. of Structural Biology, Rehovot, Israel * current address: Center for Computational and Theoretical Biology, University of Würzburg, Würzburg, Germany Abstract Osteocytes and their cell processes reside in a large, interconnected network of voids pervading the mineralized bone matrix of most vertebrates. This osteocyte lacuno-canalicular network (OLCN) is believed to play important roles in mechanosensing, mineral homeostasis, and for the mechanical properties of bone. While the extracellular matrix structure of bone is extensively studied on ultrastructural and macroscopic scales, there is a lack of quantitative knowledge on how the cellular network is organized. Using a recently introduced imaging and quantification approach, we analyze the OLCN in different bone types from mouse and sheep that exhibit different degrees of structural organization not only of the cell network but also of the fibrous matrix deposited by the cells. We define a number of robust, quantitative measures that are derived from the theory of complex networks. These measures enable us to gain insights into how efficient the network is organized with regard to intercellular transport and communication. Our analysis shows that the cell network in regularly organized, slow-growing bone tissue from sheep is less connected, but more efficiently organized compared to irregular and fast-growing bone tissue from mice.
    [Show full text]
  • Bone & Cartilage
    Compiled and circulated by Mr. Suman Kalyan Khanra, SACT, Dept. of Physiology, Narajole Raj college BONE & CARTILAGE (Structure, Function, Classification of BONE & CARTILAGE) BY Suman Kalyan Khanra SACT Department of Physiology NARAJOLE RAJ COLLEGE Narajole; Paschim Medinipur 1 | P a g e ZOOLOGY: SEM-III, Paper-C6T: Animal Physiology, Unit-2: Bone & Cartilage Compiled and circulated by Mr. Suman Kalyan Khanra, SACT, Dept. of Physiology, Narajole Raj college BONE Definition: A bone is a somatic structure that is comprised of calcified connective tissue. Ground substance and collagen fibers create a matrix that contains osteocytes. These cells are the most common cell found in mature bone and responsible for maintaining bone growth and density. Within the bone matrix both calcium and phosphate are abundantly stored, strengthening and densifying the structure. Each bone is connected with one or more bones and are united via a joint (only exception: hyoid bone). With the attached tendons and musculature, the skeleton acts as a lever that drives the force of movement. The inner core of bones (medulla) contains either red bone marrow (primary site of hematopoiesis) or is filled with yellow bone marrow filled with adipose tissue. The main outcomes of bone development are endochondral and membranous forms. This particular characteristic along with the general shape of the bone are used to classify the skeletal system. The main shapes that are recognized include: long short flat sesamoid irregular Types of bone Long bones These bones develop via endochondral ossification, a process in which the hyaline cartilage plate is slowly replaced. A shaft, or diaphysis, connects the two ends known as the epiphyses (plural for epiphysis).
    [Show full text]
  • 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.
    [Show full text]