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    NATIONAL BOARD

    HISTOLOGY REVIEW

    DEN 6416C 2012

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    MEMBRANE-BOUND ORGANELLESNucleus euchromatin (active), heterochromatin (silent)

    Mitochondrion inner membrane folded into cristae, increaseSA, produce ATP and heat, oxidize fatty acids (muscle cells,hepatocytes cells that require lots of energy)

    Lysosome contains hydrolytic enzymes, acidic interior

    Peroxisome forms and utilizes hydrogen peroxide, catalase,

    involved in lipid synthesis (e.g. hepatocytes)Smooth ER lipid synthesis, transport & storage, detox. ofmetabolites, hormones & drugs, Ca2+ storage/release (steroidhormone-producing cells)

    Rough ER ribosomes attached to cytoplasmic face of

    cisternae, protein synthesis and modification, entrance tosecretory pathway

    Golgi apparatus polarized, modifies, packages & sortsmaterials from rER intracellular use or secretory vesicles

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    NON MEMBRANE-BOUND STRUCTURES

    Nucleolus ribosomal RNA synthesis

    Ribosome large and small subunits, assemble into functionalribosome outside nucleus, fixed (to rER) or free (synthesizeintracellular components, e.g. cytoskeletal protein subunits)

    Lipid droplet energy storage depot, large unilocular (white fat)

    or small multilocular (brown fat)

    CELL SURFACE MODIFICATIONS

    Microvilli core of actin microfilaments, anchor into terminal

    web, inc. SA for absorption (e.g. small intestine)

    Cilia - core of microtubules, may be motile (e.g. conductingportion of respiratory tract)

    Stereocilia core of actin, found in male reproductive tract

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    Simple

    Squamous Cuboidal Columnar

    Stratified

    Pseudostratified

    Relaxed Distended

    EPITHELIUM

    Transitional(Respiratory-

    pseudostrat.

    ciliated with

    goblet cells)

    (Urinary)

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    EPITHELIUMSkin stratified squamous keratinized epithelium

    (stratum basale stem cells,spinosum stellate, lamellar

    bodies, desmosomes, granulosum keratohyaline granules,

    breakdown of organelles begins, lucidum breakdown of

    nuclei and organelles complete, corneum anuclear flattened

    bags of keratin)

    Mucosa of vestibule, alveolar mucosa, interdental papilla, soft

    palate - stratified squamous NON- keratinized epithelium

    Mucosa of hard palate, free gingiva and attached gingiva -

    stratified squamous keratinized / parakeratinized (also known

    as orthokeratinized epithelium)

    Stratified protection Keratinized waterproofing

    (Esophagus stratified squamous non-keratinized epithelium,

    rest of digestive tract simple columnar epithelium)

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    GLANDSExocrine secrete onto free surface

    Sebaceous gland Mammary gland Pancreas

    Goblet cell unicellular gland, multicellular glands havegroups of cells (acini) secreting into ducts

    Endocrine secrete into blood stream

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    CONNECTIVE TISSUE COMPONENTSCELLS: fibroblasts

    immunevascular

    EXTRACELLULAR MATRIX:

    Fibers - collagen, elastic,reticular (type III

    collagen)

    Ground substance -glycosaminoglycans

    proteoglycans

    adhesive proteins

    Tissue fluid

    LOOSEconnective tissue many cells, few large bundles offibers (e.g. lamina propria of intestine, papillary dermis of skin)

    DENSEconnective tissue appear to be fewer cellsinterspersed between larger bundles of fibers ( IRREGULAR

    reticular dermis of skin; REGULAR tendon, ligament)

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    COLLAGEN

    Most abundant protein in body, can be fibrillar or non-fibrillar Fibers are flexible, unbranched and have very high tensile

    strength (> stainless steel). They consist of bundles of threadlike

    fibrils bound together by non-fibrillar collagen and proteoglycans

    Fibrils are composed of arrays oftropocollagen building blocks.Tropocollagen consists of three chains (same or different)intertwined to form a triple helix

    chains consist of repeating amino acid triplets: Gly-X-Y (left).X & Y are commonly proline, hydroxyproline or hydroxylysine. -chains are modified and then assemble into procollagen

    molecules within rER

    Procollagen is secreted - ends are cleaved extracellularly byprocollagen peptidases to form mature tropocollagen

    Tropocollagen molecules cross-link in a staggered arrayresulting in a 68nm periodicity

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    ELASTIN

    Long (~750 a.a.), hydrophobic protein rich in glycine andproline - favor a compact folded conformation

    Synthesized and secreted asproelastin,cleaved totropo-elastinin extracellular space

    Contains uniquedesmosine & isodesmosineresiduesformed by covalent bonds between 4 lysines from different

    elastin chains

    Deposited initially within scaffoldings of microfibrils(composed largely of fibrillins) called oxytalan fibers.(Marfans syndrome fibrillin mutation)

    As tropoelastin is deposited, elaunin fibers are formed. As elastin accumulates and occupies the center of the

    elaunin fiber, an elastic fiber is formed.

    Elastin can occur as discrete, thin, branching fibers or asfenestrated sheets (lamellae) in the walls of large vessels

    (e.g. aorta)

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    Fibroblasts(inc. reticular cells) synthesize procollagen and

    proelastin and ground substance components

    Adipocytes - specialized for storage and release of energy

    Macrophages -differentiate from monocytes, phagocytose &

    destroy dead cells & other foreign material, present antigens toplasma cells for antibody production

    Plasma cells not present in blood, differentiate from B

    lymphocytes, synthesize and secrete antibodies

    Mast cells many large granules containing histamine, growth

    and inflammatory factors, heparin, and other proteins.

    Degranulation triggered by antigens, leads to vasodilation, inc.

    vascular permeability, bronchiolar constriction, attraction of

    other WBC

    RESIDENT CONNECTIVE TISSUE CELLS

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    Neutrophil most common WBC in blood, multilobed nucleus,

    neutral-staining specific granules, survive 1 - 4 days in CT,

    phagocytose bacteria, when dead form pus

    Eosinophil bilobed nucleus, eosinophilic (red) specific

    granules, release major basic protein which targets walls of

    parasites, phagocytose and destroy antigen-antibody complexes

    Basophil least common WBC, basophilic (blue) specific

    granules, secrete heparin and histamine that initiate, maintain

    and control inflammation

    Lymphocyte large nucleus, little cytoplasm, no visible

    granules, involved in innate and specific immune responses,

    many different types (B cells give rise to plasma cells)

    TRANSIENT CONNECTIVE TISSUE CELLS

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    CARTILAGESurrounded by a perichondrium, matrix secreted bychondroblasts, mature cells (chondrocytes) are surrounded bymatrix. Cells sit in spaces called lacunae. Cells are arranged inisogenous groups. Grows appositionally and interstitially.Avascular & aneural.

    Hyaline most common, found in mostjoints, growth plates & tracheal rings,collagen type II, smooth glassy matrix

    Elastic found in pinna of ear andepiglottis, contains collagen type II,many elastic fibers

    Fibro - intermediate between denseirregular CT and hyaline cartilage, containscollagen types Iand II, no perichondrium,Forms disc and covers articular surfaces ofTMJ, found in IV discs, pubic symphysis

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    BONECompact (outer) and spongy (inner, trabecular) bone. Surroundedby a periosteum (many cell layers), lined by endosteum (single cell

    layer). Grows only appositionally. Can form intramembraneously(from mesenchyme) orendochondrally (erosion of a cartilagemodel and deposition of bone).

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    COMPACT BONE

    Arranged incylindricalunits (calledosteons orHaversian

    systems) ofconcentriclamellae ofmineralizedmatrix andosteocytessitting inlacunae.

    Central canals (Haversian canals) contain blood vessels, nerves

    and lymphatics and are lined by endosteum.

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    BONE CELLS

    OSTEOPROGENITOR cells derived from mesenchyme,differentiate into osteoblasts, comprise the inner layer of theperiosteum and line Haversian canals and medullary cavity(endosteum)

    OSTEOBLASTS synthesize and secrete organic

    components of bone matrix, found adjacent to matrix theyhave secreted

    OSTEOCYTES individual mature bone cells that reside inlacunae (no cell nests/isogenous groups), surrounded bymatrix, cells processes sit in canaliculi allow for

    communication between, and nourishment of, cells

    OSTEOCLASTS - large, motile, multinucleate cells, derivedfrom monocytes, lie close to bone in Howships lacunae,involved in bone resorption

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    ENDOCHONDRAL OSSIFICATION

    Resting / reserve zone

    Zone of proliferation

    Zone of hypertrophy

    Zone of calcification

    Zone of vascular invasionEpiphyseal

    plate

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    SKELETAL MUSCLE ORGANIZATIONEach skeletal muscle has

    thousands of fibers huge,long multinucleate cells

    formed by the fusion of

    hundreds of embryonic

    cells.

    Each fiber is surroundedby a fine connective

    tissue sheath called

    ENDOMYSIUM.

    Several fibers are groupedtogether in a fascicle by

    collagenous PERIMYSIUM.

    Fascicles are bound by a dense fibrous connective tissue layer

    called EPIMYSIUM.

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    1 SKELETALMUSCLE FIBER = 1 CELLSkeletal muscle fibers

    contain MYOFIBRILS,long rods which fill 80%

    of the sarcoplasm.

    Myofibrils are long rows

    of repeating contractilesegments called

    SARCOMERES.

    Sarcomeres - are

    composed of regular

    arrays of thin (actin)

    and thick (myosin)

    filaments whose

    calcium-dependent

    interaction is the basis

    of contraction

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    INTERACTION BETWEEN ACTIN AND MYOSIN

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    SKELETAL MUSCLE CONTRACTION1. Nerve impulse travels down axon, Ach is released into the

    synaptic cleft, binds to receptors on the sarcolemmacausing voltage gated Na+ channels to open & Na+ toenter the muscle cell

    2. Depolarization is passed via t-tubules (sarcolemmainfoldings) to the sarcoplasmic reticulum resulting in therapid release of Ca2+

    3. Ca2+ binds to the TnC subunit of the troponin complex

    a) Troponin shifts tropomyosin deeper into groove, exposingthe myosin binding site on actin

    b) the ADP-Pi-myosin complex binds to active site on actin

    c) Pi is released

    d) myosin has conformational change and actin is pulledtoward M-line, releasing ADP

    e) ATP binds to myosin releasing it from actin

    f) ATP hydrolyzed into ADP and Pi

    4. Ca2+

    is sequestered into the sarcoplasmic reticulum

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    CARDIAC MUSCLEStriated, involuntary, centrally

    located nuclei. Fibers are short,fat, branched and interconnected.

    Cells are linked by intercalated

    discs, function as a syncytium.

    Purkinje fibers large, rich in glycogen & mitochondria,

    responsible for conducting contractile impulses

    INTERCALATED DISC

    Longitudinal portion Gapjunctions and desmosomes

    Transverse portion Fascia

    adherens and desmosomes

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    CONTRACTION OF SMOOTH MUSCLE

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    NERVE

    EPINEURIUM

    CT sheatharound several

    fascicles of

    axons

    PERINEURIUMthin, protective

    CT sheath

    around each

    fascicle

    ENDONEURIUM

    delicate

    strands of CT

    between

    individual axons

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    SCHWANN CELLS, NODES OF RANVIER

    & SCHMIDT-LANTERMAN CLEFTS

    External lamina

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    AXONAL TRANSPORT

    Internal transport system designed to move materialssynthesized in cell body (neurotransmitters, proteins)

    Transport occurs along microtubules and requires motorproteins (kinesins, dyneins)

    microtubule

    Anterograde

    Retrograde

    ANTEROGRADE & RETROGRADE TRANSPORT

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    CONDUCTING & RESPIRATORY

    PORTIONS OF THE RESPIRATORY TREE

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    Alveoli

    (surrounded byfine elastic fibers)

    Bronchus (cartilage

    & smooth muscle in

    wall, )

    Bronchiole ( no

    cartilage, just

    smooth muscle in

    wall, lined withciliated cells &

    Clara cells)

    Terminal bronchiole

    Respiratory

    bronchiole

    (alveoli off walls)

    Alveolar duct

    Alveolarcapillarynetwork

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    CELLS LINING BRONCHIOLES

    Ciliatedcell

    Basalcell

    Clara

    cell

    Clara (bronchiolar) cells columnar cells with domedapices and short blunt microvilli. Apical cytoplasm filled

    with secretory granules containing surfactant-like material

    that reduces surface tension and faciliates patency of

    bronchioles. Cells also degrade inhaled toxins.

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    Resp. bronchiole

    Alveolar duct

    Alveolar sac

    RESPIRATORY REGION OF THE LUNGSmooth muscle

    Alveolus

    Type II

    Type I cells (squamous alveolar cells) - highly attenuated, cover 97% ofsurface area of alveoli, basement membrane fuses with that of endothelial cell

    to minimize thickness of respiratory membrane.Type II cells (septal cells) account for 60% of alveolar cells but only 3% ofsurface area, produce surfactant that lowers alveolar surface tension, divideto form new Type II and type I cells.

    Alveolar macrophages (dust cells) derived from monocytes

    Type I

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    NASAL CAVITY & PARANASAL AIR SINUSES

    Respiratory area -pseudostratifiedciliated columnar epithelium with goblet

    cells, highly vascularized

    Olfactory area(roof of nasal cavity and superior concha)

    olfactory epithelium specialized bipolar (sensory) neurons with

    sustentacular (supporting) cells and basal cells (stem cells)

    SAGITTAL VIEW CORONAL VIEW

    O

    R

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    OLFACTORY EPITHELIUM

    Olfactory cells bipolar neurons, apical dendrite ends in olfactoryvesicle from which non-motile cilia with receptors for odiferous

    substances arise. When a threshold level of receptors are occupied anaction potential is generated and transmitted to the olfactory bulb viaaxon which passes through cribiform plate to synapse in olfactory bulb.Sustentacular cells tall columnar cells with microvilli. Providephysical support, nourishment & electrical insulation for olfactory cells.Basal cells stem cells to replace olfactory and sustentacular cells.Bowman

    s glands provide serous fluid to refresh olfactory cilia.

    Olfactory cell

    Sustentacular

    cell

    Bowmansgland

    Dendrite

    Olfactory vesicle

    Basal cell

    Olfactory cilia

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    CA

    RDIO

    VASCULA

    R

    VEINS ARTERIES

    CAPILLARIES

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    BLOOD VESSELSElastic arteries large arteries (e.g. aorta), have sheets /lamellae of elastin synthesized by smooth muscle cells in

    their tunica media

    Muscular arteries regulate blood flow to organs, mediamainly comprised of smooth muscle but have prominentinternal and external elastic lamellae (KNOW CELIAC

    TRUNK)

    Arterioles 1- 3 layers of smooth muscle in walls, regulateflow to capillary beds and modulate pressure

    Capillaries sites of exchange, may be continuous orfenestrated

    Veins have valves to prevent backflow, large lumenrelative to wall thickness, little muscle in tunica mediacompared to companion arteries, tunica adventitia is mostprominent layer (KNOW VEINS OF UPPER LIMB)

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    BLOOD COMPONENTSAll leukocytes have primary granules (lysosomes)Granulocytes have secondary granules (neutrophils,eosinophils, basophils)

    Neutrophil most common, multilobed nucleus, secretemyeloperoxidase, form pus

    Eosinophil - major basic protein makes holes in walls ofparasites, ingest antigen-antibody complexesBasophil rare, histamine (vasodilation, bronchioleconstriction), heparin (anticoagulant) , leukotrienes

    Lymphocyte T-cells (thymus), B-cells (bone marrow,plasma cells) NK cells destroy virus-infected /

    transformed cellsMonocyte only found in blood, transform intomacrophages in tissues

    Platelets (thrombocytes) fragments of megakaryocytes,adhere and aggregate on exposed CT surfaces, contribute

    to clot, removed by plasmin

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    REPRODUCTION

    All follicles arrested inprophase I until just beforeovulation one completes

    meiosis I and is released

    from Graafian follicle

    Empty Graafian folliclebecomes corpus luteum

    Degenerating follicle iscalled atretic follicle

    Zona pellucida glycoprotein surroundingoocyte through which spermmust penetrate to fertilize

    ovum

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    REPRODUCTION

    Male germ cellsprogress from

    spermatogonia to

    spermatocytes to

    spermatids to

    spermatozoa.Sertoli cellssupport germ

    cells, form bloodtestis barrier

    Leydig cells insurrounding CT

    producetestosterone

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    BASIC STRUCTURE OF DIGESTIVE TRACT

    WALL

    Layers: mucosa, submucosa, muscularis, serosa/adventitia

    Each region has identifying characteristics related to function

    ()

    Mucosa

    Mucosa

    Subucosa

    Muscularis

    ExternaAdventitia

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    OESOPHAGUS

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    CELLS OF STOMACH EPITHELIUM

    (HCl, intrinsicfactor)

    (pepsinogen)

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    CELLS OF STOMACH EPITHELIUM

    MUCOUS CELLS - surface mucous cells and mucous neckcells, large mucous cup at apical surface of cells, mucous

    protects epithelium from low pH and pepsin in stomach lumen

    PARIETAL (oxyntic) CELLS - produce HCl and intrinsic factor

    (vitamin B12 absorption), many mitochondria, intracellular

    canaliculi

    CHIEF (zymogenic) CELLS - secrete pepsinogen (inactive

    precursor), which is converted into pepsin (acid protease) by

    low pH. Also secrete rennin and gastric lipase.

    ENTEROENDOCRINE (APUD,DNES) CELLS - secrete gastrin

    (stimulates parietal cells) & glucagon (stimulates glucose

    release from liver). Located throughout epithelium of GI tract

    and secrete different hormones in different locations

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    AMPLIFICATION OF ABSORPTIVE

    SURFACE OF SMALL INTESTINE

    PLICAE CIRCULARES transverse folds of mucosa andsubmucosa, most prominent in jejunum ( SA 2-3 fold).

    VILLI 0.51.5 mm long epithelial-covered projections ofthe lamina propria. Core contains capillary loops,

    lymphatic channel, few smoth muscle cells embedded inloose connective tissue ( SA 10 fold).

    MICROVILLI striated border on apical surface of cells,covered in enzyme-containing glycocalyx ( SA 20 fold).

    Total increase in surface area ~ 600 fold

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    VILLI & INTESTINAL GLANDS

    DUODENUMLeaf-shaped villi,

    *mucus-secreting

    Brunners glands

    in submucosa*

    JEJUNUMFinger-shaped

    villi, no glands

    in submucosa

    ILEUMVilli shorter than in

    jejunum. Peyerspatches in lamina

    propria & submucosa

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    COLON

    Lumen

    Longitudinal m

    Circular m

    Submucosa

    Tenia coli

    Mucosa

    Absorbs water and ions from chyme it receives from the small

    intestine and compacts chyme into feces for elimination.

    Large intestine has NO villi but has Crypts of Lieberkuhn.

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    EPITHELIAL CELL RENEWAL

    Stem cells undifferentiated, capable of self renewal

    Stomach stem cells found in neck of gland

    Small intestine stem cells found in Crypts of Lieberkuhn

    Large intestine stem cells found in lower half of glands

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    MUCOSA: Wet membrane that opens to the outside

    Small intestine

    Hard palate andgingiva:

    masticatory mucosa

    Small intestineCheeks, soft palate,floor of mouth, lips:

    lining mucosa

    Type CT depends on functional forces exerted on mucosa

    Consists of epithelium and underlying CTForms an impenetrable barrier

    DCT

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    Skin

    Mucosa

    (Non-keratinized SSE)

    Para-k

    MC Junction

    Parakeratinized region of skin

    Skin(Keratinized SSE))

    MUCOCUTANEOUS JUNCTION

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    COMPONENTS OF A SALIVARY GLAND

    Striated duct

    Serous acinus

    Serous demilune

    Submandibular gland

    Mucous cells

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    ACINUS & DUCT SYSTEM OF A SALIVARYGLAND

    Striated duct(Intralobular) Excretory duct(Interlobular)

    Intercalated duct

    (Intralobular)

    Outside of lobuleWithin lobule

    HypotonicSalivaCl-

    Striated duct

    Na+

    K+

    Interlobular duct

    HCO3

    Acinus Intercalated duct

    LUMEN

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    Parotid- 25% of saliva, largest gland,predominantly serous, secretes into

    Stensons duct, well developed striatedducts, synthesizes amylase and

    transports secretory IgA synthesized byplasma cells into saliva prevents

    adhesion of bacteria and viruses to oral

    mucosa

    Sublingual (5% of saliva), smallestgland, secretes into ducts of Rivini

    (plicae sublingulares), predominantly

    mucous secreting, poorly developed

    striated ducts

    Submandibular (70% of saliva),mixed gland, secretes into Whartonsduct, well developed striated ducts,

    makes lysosyme which hydrolyses

    walls of bacteria

    Serous demilune

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    BUD STAGE

    RECIPROCAL INDUCTION

    Condensedectomesenchyme

    Epithelialtooth bud

    Dental lamina

    Bone

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    CAP STAGE

    Dental lamina

    Supporting

    structures

    Dentin

    & pulp

    Enamel

    Dentalfollicle

    Dentalpapilla

    Enamelorgan

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    CAP - BELL STAGE

    Dentalpapilla

    Oral cavity

    Outer dentalepithelium

    Dental lamina

    Stellatereticulum

    Stratum

    intermedium

    Inner dentalepithelium

    Cervicalloop

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    LATE BELL EARLY

    APPOSITION

    Collapsed

    enamel organ

    Pulp

    Cervical loop

    ODESR

    Dentin

    Odontoblasts

    Enamel

    AmeloblastsStratum

    inter-

    medium

    Pulp

    Predentin

    SR

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    SECRETORY AMELOBLAST

    DISTAL END

    Formsinterrod

    substanceProximal portion

    Formsenamel rod

    Forms rodsheath

    Junctionalcomplex

    Stratum intermedium Ameloblast body Tomes process

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    Rod

    T.E.M. OF ENAMEL

    Cylindrical rods are composed of long crystals that run parallel to the

    longitudinal axis of the rod. Rods are embedded in interrod enamelwhose crystals run in a different direction. Rod and interrod enamel

    are separated by a thin rod sheath containing organic material.

    Mineralization may be nucleated by apatite crystals in dentin. Non-

    amelogenins regulate mineralization, amelogenins regulate growth in

    thickness and width of the crystals.

    Rod sheath

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    ENAMELMost highly mineralized tissue in the bodyComposed of 96% hydroxyapatite crystals, 4% proteins & H2OCovers anatomical crownExtremely brittle, supported by underlying resilient dentinSynthesized by ameloblasts which are lost after eruptionIncapable of repairLong crystals arranged in rods separated by interrod enamelInner and outermost layers of enamel are aprismaticPartially mineralized (30%) enamel deposited first, followed byreplacement of organic material by additional mineral.Enamel proteins (amelogenins (bulk), tuftelin (just at DEJ), enamelin(2%), ameloblastins (5-10%)) play important role in regulation of

    mineralization. Crystallites are formed almost immediately within

    enamel proteins; no equivalent of predentin or osteoid

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    STRIAE OF RETZIUS &

    CONTOUR LINES OF OWEN

    Striae of Retzius (B)Series of dark lines extending from the

    dentino-enamel junction (DEJ) to the tooth

    surface (where they end in perikymata).

    Caused by metabolic changes that occur

    while enamel is being deposited that result

    in hypomineralization. The thickest,darkest one, the neonatal line, reflects the

    physiological changes which occur around

    the time of birth.

    Contour Lines of Owen (A)

    Analagous to Straie of Retzius but formedin dentin. Both formed at the same stage

    of development and meet at the DEJ.

    (Hypomineralized regions appear darker)

    DEJ

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    ENAMEL SPINDLES, TUFTS & LAMELLAE

    all hypomineralized areas of enamel

    Dentinwith dentinal

    tubules

    Enamel

    Enamel tuft

    rich in enamelproteins

    Enamel spindle tip of odontoblastprocess trapped in enamel

    Enamellamella

    region

    containing

    trapped

    organicmaterial

    DEJ

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    DENTINForms bulk of tooth, supports the overlying brittle enamelHard, elastic, avascular tissue that encloses the pulp chamberComposed of 65-70% hydroxyapatite crystals, 20-25% organicmaterial (collagen, PGs, glycoproteins) & ~ 10% water

    Coronal under crown, radicular under cementumOrganic components synthesized and maintained byodontoblasts at boundary of dental pulp which persist after

    eruption

    Contains closely packed tubules which house cytoplasmicextensions of odontoblastsTubules extend from the pulp to the dentinoenamel junction(DEJ) or dentinocemental junction (DCJ)

    Capable of repair (tertiary or reparative dentin)Sensitive

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    DENTINOGENESISPolarized nucleus rER Golgi Junctional complex Peritubular dentin

    MineralizationPredentinOdontoblastic layerCell rich

    zoneCell-free

    zone

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    Intertubular dentin

    DENTINAL TUBULES

    Dentinal tubules canaliculi that traverse dentin, housed odontoblastic

    processes. Peritubular dentin collar of highly mineralized dentin

    surrounding the tubule. Intertubular dentin located between tubules,

    less mineralized than peritubular dentin, 1st secretory product of

    odontoblasts, fibrils arranged at right angles to dentinal tubules.

    Dentinal tubule

    Peritubular dentin(Intratubular dentin)

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    GLOBULAR & INTERGLOBULAR DENTIN

    Mineralized dentin

    Mineralization front

    Predentin

    Dentin is mineralized after it isformed. This begins in small

    spherical areas which become

    larger and fuse with one another

    to form a mineralization front.

    Enamel rods

    Interglobular dentin

    DEJ

    Interglobular dentin refers to areasof hypo- or non- mineralized dentin

    where globular zones of minerali-

    zation have failed to fuse within

    mature dentin. Tubules can pass

    through but no peritubular dentin

    exists where they do.

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    FORMS OF

    DENTIN

    Mantle dentin part of

    primary, laid down first,

    mineralizes differently

    Tertiary dentin reparative,

    may not have tubules

    Primary dentin

    circumpulpal, laid down first

    Secondary dentin laiddown after root formation,

    less permeable than primary

    dentin

    Predentin unmineralized

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    SCLEROTIC DENTINIf dentin is damaged the

    odontoblastic processes dieleaving empty dentinal

    tubules which form areas of

    dead tracts (A).

    Dead tracts become filled withmineral and are called blind

    tracts (B).

    The dentin of blind tracts is

    known as sclerotic dentin.

    ROOT FORMATION

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    ROOT FORMATION

    Cervical loop reflection of outer to

    inner dental epithelium. Grows down

    to form Hertwigs epithelial root sheath which outlines future root andsecretes factors which induce root pulp cells to differentiate into

    odontoblasts. Sheath then breaks up, leaving isolated epithelial cell

    rests of Mallassez that lie between fibers of PDL.

    PDL

    RootcanalCementum

    Attachment organODE

    IDE

    Cervicalloop

    ATTACHMENT ORGAN & JUNCTIONAL

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    ATTACHMENT ORGAN & JUNCTIONALEPITHELIUM (JE)

    Circular arrangement of epithelialcells at the base of gingival sulcus

    (JE) attaches to both the tooth

    (enamel) and underlying connective

    tissue, forming a protective seal

    between the oral cavity & underlying

    tissues.JE is formed during tooth eruptionby fusion of reduced enamel

    epithelium and overlying oral

    epithelium and thus has two basal

    laminae; one at each surface.

    JE cells constantly renewed underinfluence of factors secreted by

    underlying CT cells.

    Basal laminae

    shown in green

    JE

    3-4 cells thick

    15-30cells thick

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    GROUPS OF FIBERS WITHIN GINGIVA

    CEMENTUM

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    DCJ

    Cellular

    cementum synthesized

    rapidly

    around apical

    1/3 of roots of

    premolars

    and molars

    after teeth are

    in occlusion.

    Cells become

    trapped in

    matrix.

    CEMENTUM

    Dentin

    Acellular

    cementum

    deposited

    around roots

    of all teeth.Cells do not

    become

    trapped but

    move further

    away from the

    DCJ.

    Granular Layer of Tomes small

    hypomineralized areas reflecting

    arrangement of matrix proteins at

    the dentino-cemental interface

    Cementoblasts differentiate from cells of the dental follicle after

    exposure to dentin following the breakdown of Hertwigs epithelialroot sheath

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    PERIODONTAL LIGAMENT

    Attaches tooth to alveolar bone via collagen fibers anchoredinto cementum or alveolar bone as Sharpeys fibers. PDL fibersdo not become oriented until tooth is in occlusion. Mostly

    collagen fibers (types I, III & XII), also oxytalan fibers. PDL

    permits tooth to withstand forces of mastication. Also sensory

    role. High rate of turnover.

    Dentin

    Cementum

    Bundle bone

    PDL(Major fiber bundle)

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    GROUPS OF FIBERS WITHIN PDL

    Alveolar crest fibers just belowCEJ to rim of alveolus

    Horizontal fibers below apicalgroup, run from cementum to bone

    just below alveolar crest

    Oblique fibers most numerous,

    run from cementum into alveolarbone, greatest support againstmasticatory forces, resist movementof tooth in apical direction

    Apical fibers radiate from

    cementum around the apex of theroot to the bone, resist movement oftooth in an occlusal direction

    Interradicular fibers found onlybetween roots of multirooted teeth,run from cementum into bone