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Quiz

Bone and Cartilage

Kissa Walker 10 Fragen

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  1. 1[blank_start]chondroblasts[blank_end] = produce matrix; undifferentiated cells
    [blank_start]chondrocyte[blank_end] = mature chondroblasts surrounded by matrix
    [blank_start]lacunae[blank_end] = space the cell sits in
    [blank_start]isogenous groups[blank_end] = dividing cartilaginous cell
    [blank_start]perichondrium[blank_end] = denser tissue around cartilage; vascular supply; [blank_start]outer layer[blank_end] = dense connective tissue and fibroblasts; [blank_start]inner layer[blank_end] = chondroblasts
    1. Achondroblasts
    2. Bchondrocyte
    3. Clacunae
    4. Disogenous groups
    5. Eperichondrium
    6. Fouter layer
    7. Ginner layer
  2. 2[blank_start]histogenesis[blank_end] = growth of tissue - derived from [blank_start]mesenchyme[blank_end] - undifferentiated, condense and become [blank_start]chondroblasts[blank_end]; [blank_start]chondrocytes[blank_end] will form [blank_start]isogenous groups[blank_end].

    [blank_start]interstitial growth[blank_end] = mitotic division of chondrocytes - growth plate for long bone; only in cartilage

    [blank_start]appositional growth[blank_end] = differentiation of perichondrial cells - growth in girth; bone
    1. Ahistogenesis
    2. Bmesenchyme
    3. Cchondroblasts
    4. Dchondrocytes
    5. Eisogenous groups
    6. Finterstitial growth
    7. Gappositional growth
  3. 3ECM:
    fibrils = [blank_start]collagen type I[blank_end]; [blank_start]collagen type II[blank_end]; [blank_start]elastin[blank_end]
    connectors = [blank_start]collagen type IX, X, XI[blank_end]
    ground substance = [blank_start]hyaluronic acid[blank_end] - non-sulphated unit of GAG; [blank_start]GAG[blank_end] - side chains of proteoglycans, hydrophilic, chondroitan sulphate, keratan sulphate; [blank_start]proteoglacans[blank_end]; [blank_start]glycoproteins[blank_end]

    1. Acollagen type I
    2. Bcollagen type II
    3. Celastin
    4. Dcollagen type IX, X, XI
    5. Ehyaluronic acid
    6. FGAG
    7. Gproteoglacans
    8. Hglycoproteins
  4. 4Types of cartilage:
    [blank_start]hyaline[blank_end] = fibrils - collagen type II, ground substance; fetal skeleton, synovial joints, trachea, larynx, nose, epiphyseal plate
    [blank_start]elastic[blank_end] = fibrils - collagen type II, ground substance; external ear, external auditory meatus, auditory tubes, epiglottis
    [blank_start]fibrocartilage[blank_end] = fibers - collagen type I, ground substance; intervertebral discs, tendons and ligaments, symphysis pubis

    1. Ahyaline
    2. Belastic
    3. Cfibrocartilage
  5. 5[blank_start]osteoblasts[blank_end] = secrete matrix - not mineralized; type I collagen, proteoglycans, glycoproteins
    [blank_start]osteocyte[blank_end] = mature cell, surrounded by matrix, reside in lacunae, canaliculi is cytoplasmic processes
    [blank_start]osteoclast[blank_end] = reabsorb matrix, mutlinucleated, remodel bone, release building blocks
    1. Aosteoblasts
    2. Bosteocyte
    3. Costeoclast
  6. 6[blank_start]osteonectin[blank_end] - promote calcification of the matrix
    [blank_start]periosteum[blank_end] - outer layer - collagen fibers and fibroblasts; inner layer - osteoprogenitor cells
    [blank_start]endosteum[blank_end] - single layer, osteoprogenitor cells, internal cavities of bone
    1. Aosteonectin
    2. Bperiosteum
    3. Cendosteum
  7. 7[blank_start]primary bone[blank_end] = random collagen fibers; lower mineral content
    [blank_start]secondary bone[blank_end] = lemellar collagen arrangement; haversian system - osteon
    1. Aprimary bone
    2. Bsecondary bone
  8. 8intramembranous ossification:
    primary center of ossification - [blank_start]mesenchymal cells[blank_end] into [blank_start]osteoblasts[blank_end]; direct mineralization of matrix

    IO Abnormalities:
    [blank_start]Crouzon's Syndrome[blank_end] - cranial synostosis, exophthalmos, short upper lip, mutation in FGF rceptor 2
    [blank_start]Apert Syndrome[blank_end] - facial bones, skull and mid facial abnormalities, syndactyl, mutation in FGF receptor 2
    1. Amesenchymal cells
    2. Bosteoblasts
    3. CCrouzon's Syndrome
    4. DApert Syndrome
  9. 9Endochondral Ossification: - [blank_start]long bones[blank_end]
    [blank_start]ossification[blank_end] zone; [blank_start]calcified[blank_end] cartilage zone - osteoclasts, osteoblasts; [blank_start]hypertrophic cartilage[blank_end] zone - bid cells, type X collagen

    EO Abnormalities:
    [blank_start]osteogenesis imperfecta[blank_end] - brittle bone, abnormality in type I collagen
    1. Along bones
    2. Bossification
    3. Ccalcified
    4. Dhypertrophic cartilage
    5. Eosteogenesis imperfecta
  10. 10Joints:
    [blank_start]synotosis[blank_end] - bone united by bone tissue
    [blank_start]synchondroses[blank_end] - [blank_start]primary[blank_end] cartilagenous joints - bone joined by hyaline cartilage
    [blank_start]symphysis[blank_end] - secondary cartilagenous joints - bone joined by fibrocartilage
    [blank_start]syndesmosis[blank_end] - bones connected by interosseous ligament or fibrous membrane
    [blank_start]diarthroses[blank_end] - ligaments and a capsule of connective tissue contact ends of bone
    1. Asynotosis
    2. Bsynchondroses
    3. Cprimary
    4. Dsymphysis
    5. Esyndesmosis
    6. Fdiarthroses

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Beschreibung
biology SPOM (Celleular Anatomy) Quiz am Bone and Cartilage, erstellt von Kissa Walker am 28/09/2015.
Sprache
English
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Schlagwörter
spomcelleular anatomybiology
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