2013 histology review-1
TRANSCRIPT
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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