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Innervation
free nerve endings un-myelinated axons
depends on location of the epithelium and its exposure to stimuli
Renewal
Epithelia continuously renew their cell population
Different rates: fastest small intestine, slowest- skin
Metaplasia
=transformation into another type of mature epithelium, in pathological
circumstances
Tissue has the ability to transform into a different tissue if something
goes wrong. Can be reversed if the stimulus goes away.
E.g.
2. Polarity of epithelial tissue and epithelial cell. Differences between apical and
latero-basal domains of epithelial cells (Fares and Jamal)
Polarity is due to organelle distribution and membrane protein distribution
(membrane domain)
Apical domain: Proteins enzymes, transporters, channels
Lipids Cholesterol, sphingomyelin
Baso-lateral domain: Proteins Na+/K+ ATP-ase, transporters, channels,
receptors
Lipids Phosphatidylcholine, phosphatidylinositol
Specialisations: Apical pole cilia, stereocilia, microvilli
Basolateral pole lateral interdigiations and basal labyrinth
& lamina
Baso-lateral pole
Apical domain
Enzymes
Transporters
Channels
Baso-lateral domain
Na+/K+ ATP-ase
Transporters (am.ac.,
sugars)
Channels
Lipids
Cholesterol
Sphingomyelin
Receptors
Adhesion proteins
Phosphatidylcholine
Phosphatidylinositole
Types of
cilia:
1. Tight Junctions:
Impermeable and allow epithelial cells to function as a barrier.
2. Anchoring Junctions:
Provide lateral adhesions between epithelial cells, using proteins that link
into the cytoskeleton of adjacent cells.
zonula adherens ( pl., zonulae adherentes), which interacts with the
network of actin filaments inside the cell; and
macula adherens (pl., maculae adherentes) or desmosome, which
interacts with intermediate filaments
3. Gap junctions
Permit the direct passage of signalling molecules from one cell to another.
6 subunits (connexions) => connexons => gap junction
Allows cells to function together
(Basal pole)
1. Focal adhesions
Anchors actin of the cytoskeleton in the cell to the extracellular matrix
2. Hemidesmosomes
Anchors intermediate filaments of the cytoskeleton to the extracellular
matrix
Epithelium of ovary
Functions are secretion and absorption
Simple columnar: Located in digestive tract, fallopian tubes, excretory ducts
of salivary glands
Has apical surface specializations (cilia and microvilli), for
absorption,secretion
Mixed gland
- By secretion mechanism merocrine (exocytosis of stored granules)
- Apocrine (secretion of both product and apical
cytoplasm)
- Holocrine (destruction of entire cell during secretion)
- Location:
epithelium
Somatostatin (D Cells)
VIP (D1 Cells)
Serotonin (EC Cells)
Colecistochinin (I Cells)
GIP (K Cells)
Motilin (Mo Cells)
Neorotensin (N Cells)
Secretin (S Cells)
- Uniferous tubules
- Excretory ducts, salivary glands
- Digestive tract
Secretion:
CONNECTIVE TISSUE
22. Definition, basic structure and functions of connective tissues.
Characteristics:
- common embryological origin = mesoderm
- Innervated + Vascularized (direct blood supply)
* cartilage is only exception with no capillary beds *
-EC matrix - ground substance (gelatinous glycoproteins)
- structural fibers (fibrous proteins eg: collagen, elastin,
reticulin)
Types:
-Connective Tissue Proper
- loose
- dense (fibrous) irregular
- dense (fibrous) regular
- Specialized Connective Tissue:
-adipose tissue
- reticular
- elastic
- cartilage (hyaline, elastic, fibrocartillage)
- bone
- blood
forms fibrils
In: hyaline + elastic cartilage
In: reticular lamina + reticular connevtive tissue
First collagen secreting in wound healing
Forms a network in basal laminae of epithelia
Types IX + XII
Type IV
Type VII
Structure
Ultrastructure
1. Many granules
2. extensive Golgi complex
3. cisternae of RER
4. free ribosomes, mitochondria and numerous microvilli and folds.
5. Rich in Histamine & Heparin
Functions
Notes Very similar to basophil (both in function and appearance), it is located in most of
the loose connective tissue along blood vessels.
Structure
Ultrastructure
Extensive Golgi complex, abundant RER, secretory granules (Russel bodies), free
ribosomes & methachondria.
Functions
Mainly secrete immunoglobulins (antibodies): IgM, IgG, IgA, IgE, they originate in B
lymphocytes that are terminally differentiated as a result of a response to an
antigen challenge.
Structure
Localization
Structure
Few cells (compared to loose CT), mainly fibrocytes (occasional mast cells &
macrophages)
Clear predominance of collagen fibers
Few ground substance
Less flexible thus more resistant to stress
The collagen fibers are bundled WITH NO DEFINITE ORIENTATION (hence
labelled irregular)
Three deminsional network > Resistant to stress from all angles
Localization
Capsules of the parenchimatose organs
Dermis
Submucosa of the digestive tract
Periosteum
Perichondrium
Structure
Localization
Structure
inextensible structure that attaches striated muscle to bone (or other muscles)
Thick and predominant collagen fibers
Multiple layers:
Parallel in the same layer
perpendicular on the collagen fibers from the layers above and beneath
(textile aspect)
Fibrocytes - Flattened, narrow shaped
Note - the fastest and easiest way to identify on a slide is to pay
attention to the textile orginization of the collagen fibers
Localization
Between muscle and bones (and sometimes between muscles and other muscles or
structures, basically attaches the epiphysis of the bone to other structures)
Structure
Localization
Framework of the bone marrow and lymphoid tissue (lymph nodes, spleen),
supports the soft organs in the periphery.
Structure
Localization
Structure
Gelatin-like extracellular matrix (very loose)
Abundance of amorphous ground substance (also know there as
wharton's jelly)
Thin collagen fibers
Spindle shaped cells (mesenchymal cells)
Localization
Umbilical chord
Structure
Localization
Structure
Localization
essential for classical nonshivering thermogenesis (this phenomenon does not exist
in the absence of functional brown adipose tissue), as well as for the cold
acclimation-recruited norepinephrine-induced thermogenesis. Heat production from
brown adipose tissue is activated whenever the organism is in need of extra heat,
e.g., postnatally, during entry into a febrile state, and during arousal from
hibernation, and the rate of thermogenesis is centrally controlled via a pathway
initiated in the hypothalamus. Feeding as such also results in activation of brown
adipose tissue; a series of diets, apparently all characterized by being low in
protein, result in a leptin-dependent recruitment of the tissue; this
metaboloregulatory thermogenesis is also under hypothalamic control. When the
tissue is active, high amounts of lipids and glucose are combusted in the tissue. The
development of brown adipose tissue with its characteristic protein, uncoupling
protein-1 (UCP1), was probably determinative for the evolutionary success of
mammals, as its thermogenesis enhances neonatal survival and allows for active
life even in cold surroundings.
Structure
CELLULAR COMPARTMENT:
Chondroblasts
Chondrocyte
Found in matrix cavities -lacunae
Arranged in isogenous groups (clusters or columns)
Perichondrium cells
MATRIX
Territorial matrix
interterritorial matrix
Components:
1. Fibers: collagen II.
2. Ground substance
Localization
Structure
Localization
Epiglottis
Larynx (arytnoid cartilage)
Pinna of the ear, auditory canal, eustachin canal
49. Fibrous Cartilage: structure, localization
Structure
Nuclei:
Round and
basophilic
Euchromatic
(active)
1-2 nuclei
Cytoplasm:
Basophilic
Juxtanuclear pale
Ultrastructure
RER, Golgi,
Mitochondria,
glycogen, lipid
droplets all
present
Many short
cytoplasmic
projections
Localization
Cells are
isolated
located at
the
periphery
under the
perichondri
um
*Found in lacunae
region
Chondrocyte
Nuclei:
Round and
basophilic
Cytoplasm:
Acidophilic
Few organelles
Increased:
Glycogen
Lipid
droplets
Decreased:
Synthesis
AFTER they
secrete matrix
therefore most
peripheral
chondroblasts
arent in lacunae
Cells form
groups
centrally.
*Completely fill
lacunae
Both secrete all components of the matrix (fibres and ground substance)
The feature that distinguishes bone from other connective tissues is the
mineralization of its matrix, which produces an extremely hard tissue capable of
providing support and protection.
The mineral is calcium phosphate in the form of hydroxyapatite crystals
Forms of bone:
1. Microscopic
Form of bone
Primary (immature, woven)
General description
Irregular array of collagen fibres
Higher proportion of osteocytes
Lower mineral content
Regular bands of collagen fibres
arranged in sheets (lamellae)
2. Macrocopic
Form of bone
Compact (Dense) bone; C.B
Description
A compact, dense layer forming
the outside of the bone.
Structure
Osteoblast
Shape: columnar,
cuboidal (matrix
synthesis), flattened
(inactive)
Nucleus:
Pale staining
Multiple
Cytoplasm:
Basophilic
Cytoplasmic
processes =>
contact with
neighbouring cells
Osteocyte
Shape:
Ultrastruct
ure
RER, Golgi,
Mitochondr
ia
Reduced
Localizatio
n
Lining
bone
(endosteu
m,
periosteu
m,
trabeculae
,
metaphysi
s); I.e
sites of
bone
where
remodellin
g is not
occurring
Located
Functions
NOT cell
division
Synthesize
the organic
component
s of matrix
Osteocytes
Osteoclast
Flattened
Elongated
Nucleus:
Flattened
Condensed chromatin
Cytoplasm:
Less basophilic and
more acidophilic
LONG, thin
cytoplasmic
processes=> enter
matrix canaliculi =>
adjacent cells make
contact via gap
junctions
Large
Multi-nucleated
Cytoplasm:
acidophilic
organelles
between
layers of
osteon( c
oncentric
arrangem
ent of
bone
tissue
around
blood
vessels)
and
occupy
lacunae
can
synthesize
new matrix
Numerous
lysosomes
Found at
sites
where
bone is
removed
Responsible
for bone
resorption
Stages:
1. Group of mesenchymal cells differentiate osteoblasts; secrete matrix which
then becomes mineralized
2. Islands of developing bone (SPICULES);
3. Fusion of Spicules TRABECULAE in CANCELLOUS (spongy) bone
4. Growth and fusion of trabeculae COMPACT bone
54. Endochondral bone formation
Definition: Mesenchymal cells differentiate into chondroblasts that, in turn,
produce cartilage matrix.
Stages:
The process begins with the formation of a cartilage model
1); A periosteal (perichondrial) collar of bone forms around the diaphysis (shaft) of
the cartilage model
(2); then, the cartilaginous matrix in the shaft begins to calcify
(3). Blood vessels and connective tissue cells then erode and invade the calcified
cartilage
(4), creating a primitive marrow cavity in which remnant spicules of calcified
cartilage remain at the two ends of the cavity. As a primary center of ossification
develops, the endochondral bone is formed on spicules of calcified cartilage. The
bone at the ends of the developing marrow cavity constitutes the metaphysis.
Periosteal bone continues to form
(5); the periosteal bone is formed as the result of intramembranous ossification.
Blood vessels and perivascular cells invade the proximal epiphyseal cartilage
(6), and a secondary center of ossification is establishedin the proximal epiphysis
(7). A similar epiphyseal (secondary) ossification center forms at the distal end of
the bone
(8), and an epiphyseal cartilage is thus formed between each epiphysis and the
diaphysis. With continued growth of the long bone, the distal epiphyseal cartilage
disappears
(9), and finally, with cessation of growth, the proximal epiphyseal cartilage
disappears
(10). The metaphysis then becomes continuous with the epiphysis. Epiphyseal lines
remain where the epiphyseal plate last existed.
55. Composition of plasma
56. Erythrocytes
to be used as a
cells:
macrocytes > 9 m,
microcytes < 6 m
anisocytosis = variation in size
Structure
Biconcave disc
folding increases
surface area (30%
more surface area)
composition of
plasma membrane
gives flexibility
(squeeze through
capillaries)
97% hemoglobin
Ultrastructure
No nucleus
No centrioles
No organelles
No mitochondria
Function
no cell division (as
a result of no
centrioles, nuclei
or organelles)
no mitochondria
means they can
generate ATP
anaerobically =>
prevents
consumption of the
O2 that they
transport
Transport O2
Ultrastructure
Nucleus:
Has heterochromatin at
the periphery and
euchromatin more
centrally
Small golgi apparatus
Functions
Neutrophils are active
phagocytes that utilize a
variety of
surface receptors to
recognize bacteria and
other infectious
connected by
chromatin
Cytoplasm:
Contains specific
granules => cell is
Granulocyte
Granules have
affinity for Both
basic and eosin
dyes.
Ultrastructure
Nuclues:
Heterochromatin also
located at the periphery
and euchromatin
centrally
Granules:
- Specific (basophilic)
- Azurophilic (non specific
lysosomes found in all
leukocytes)
Functions
Basophils bind an
antibody
IgE, through high-affinity
Fc receptors expressed
on their cell surface. The
subsequent exposure to,
and reaction
with, the antigen
(allergen) specific for IgE
triggers the activation of
basophils and the release
of vasoactive agents
from cell granules.
Ultrastructure
Nucleus:
As in neutrophils, the
compact heterochromatin
of eosinophils is adjacent
to the nuclear envelope,
whereas the euchromatin
Functions
Eosinophils are
associated with allergic
reactions, parasitic
infections, and chronic
inflammation.
lobed
Cytoplasm:
Contains large
acidophilic granules
which cover the
cytoplasm=> cannot see
whether the cytoplasm is
acidophilic or basophilic
Ultrastructure
Organelles:
Golgi apparatus
and centrioles are
located in the
indented area
around the nucleus
RER, SER and
small mitochondria
Granules:
Azurophilic
granules
(lysosomes
contained in all
leukocytes)
Functions
During inflammation, the
monocyte leaves the
blood vessel at the site of
inflammation,
transforms into a
tissue macrophage,and
phagocytoses bacteria,
other cells, and tissue
debris.
Remain in the
blood for only
about 3 days.
Ultrastructure
Organelles:
Golgi, ribosomes,
mitochondria all
vary in amount
according to size
of lymphocyte
Functions
Immunocompetent
cells (i.e., cells that have
developed
the capacity to recognize
and respond to antigens
and are
in transit from one
micrometres
Nucleus:
Round
Mononuclear
(non-segmented)
Basophilic
Large and occupies
most of the cell
Cytoplasm
Appears as a
small, blue ring
around nucleus
(contains only
azurophilic
granules
Ribosomes =>
blue appearance
due to slight
basophilia
Granules:
Azurophilic
lymphatic tissue to
another)
Functionally different
lymphocytes:
T cells have a long life
span and are involved in
cell mediated
immunity.
B cells have variable
life spans and are
involved in the
production of circulating
antibodies.
NK cells are
programmed during their
development to
kill certain virus-infected
cells and some types of
tumor
cells.
They also secrete
an antiviral agent,
interferon
Ultrastructure
Structural organization of
the thrombocyte
cytoplasm categorized
into four zones
The peripheral zone
consists of the cell
membrane
covered by a thick
surface coat of
glycocalyx.
- The integral
membrane
glycoproteins
function as
receptors in
Functions
Continuous surveillance
of blood vessels,
Blood clot formation,
Repair of injured tissue.
platelet function.
The structural zone
comprises microtubules,
actin filaments, myosin,
and actin-binding
proteins that form a
Network supporting the
plasma membrane.
- responsible for
maintaining the
platelets disc
shape.
The organelle zone
occupies the center of
the platelet. It
consists of mitochondria,
peroxisomes, glycogen
particles,
and at least three types
of granules dispersed
within the
cytoplasm.
The membrane zone