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School of Anatomy and Human Biology - The University of Western Australia |
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hosted by the University College Cork Blue Histology - Epithelia and Glands |
| Topics |
Lab Guides and Images |
| Simple Squamous and Simple Columnar
Epithelia |
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| Stratified Squamous and Stratified
Columnar Epithelia |
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| Transitional and Pseudostratified
Epithelia |
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| Tubular Glands |
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| Large Serous and Mucous Glands |
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Epithelia are tissues consisting of closely apposed cells without intervening intercellular substances. Epithelia are avascular, but all epithelia "grow" on an underlying layer of vascular connective tissue. The connective tissue and the epithelium are separated by a basement membrane. Epithelium covers all free surfaces of the body. Epithelium also lines the large internal body cavities, where it is termed mesothelium. Furthermore, the internal surfaces of blood and lymph vessels are lined by epithelium, here called endothelium.
Epithelia are classified on the basis of the number of cell layers and the shape of the cells in the surface layer.
This type is composed of a single layer of flattened, scale- or plate-like cells. It is quite common in the body. The large body cavities and heart, blood vessels and lymph vessels are typically lined by a simple squamous epithelium. The nuclei of the epithelial cells are often flattened or ovoid, i.e. egg-shaped, and they are located close to the centre of the cells.
Cells appear cuboidal in sections perpendicular to the surface of the epithelium.
Viewed from the surface of the epithelium they look rather like small polygons.
Simple cuboidal epithelium occurs in small excretory ducts of many glands,
the follicles of the thyroid gland, the tubules
of the kidney and on the surface of the ovaries.
Can there be "low
cuboidal" epithelia?
The cells forming a simple columnar epithelium are taller than they are wide. The nuclei of cells within the epithelium are usually located at the same height within the cells - often close to the base of the cells. An example is the simple columnar epithelium which lines the internal surface of the gastrointestinal tract (GIT) from the cardia of the stomach to the rectum.
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Identifying Epithelia It is often helpful to look at the shape, location and spacing of the nuclei in the epithelium, which together will allow a very good guess at the shape of the cells forming the epithelium. |
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How many cell layers seem to be visible in a section depends very much on the angle between the plane of the section plane the surface of the epithelium. Oblique sections of epithelium will be visible in almost all slides of organs in which epithelium lines a surface with a very irregular profile. A single surface is usually not lined by several types of epithelia. The number of epithelial cell layers will usually be the smallest number of layers visible anywhere along the surface lined by the epithelium. |
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Sublingual Gland, Human, H&E |
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Duodenum, Rat, H&E and Ileum,
Human - H&E |
Stratified squamous epithelia vary in thickness depending on the number
of cell layers present. The deepest cells, which are in contact with the
basement membrane, are cuboidal or columnar in shape. This layer is usually
named the basal cell layer, and the cells
are called basal cells. Basal cells are
mitotically active and replace the cells of the epithelium which are lost
by "wear and tear". The basal cell layer is followed by layers of cells
with polyhedral outlines. Close to the surface of the epithelium, cells
become more flattened. At the surface of the epithelium, cells appear like
flat scales - similar to the epithelial cells of simple squamous epithelia.
Remember that it is the shape of the cell which
form the surface of the epithelium which gives the name to the epithelium.
are not common. A two-layered cuboidal epithelium is, for example, seen in the ducts of the sweat glands. Stratified columnar epithelia are found in the excretory ducts of the mammary gland and the main excretory duct of the large salivary glands.
| Oesophagus, human - H&E |
Parotid Gland, Human - H&E
Stratified columnar epithelia are found in the largest excretory ducts of some
glands. The parotid gland, a large salivary gland, is one of them. Several epithelial
types are found in the duct system of the parotid. The smallest ducts, which
are embedded in the secretory tissue (intralobular ducts), are lined by cuboidal
or columnar epithelia. Small ducts, which are embedded in connective tissue
located between areas of secretory tissue (interlobular ducts), are lined by
columnar or pseudostratified epithelia. These ducts finally coalesce to form
the main excretory duct of the parotid which is lined by a stratified columnar
epithelium.
Draw the stratified columnar epithelium seen in the largest
ducts and label your drawing.
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These two types of epithelia are difficult to classify using the shape of the cells in the surface layer and the number of the cell layers as criteria.
Transitional epithelium is found exclusively in the excretory urinary passages (the renal calyces and pelvis, the ureter, the urinary bladder, and part of the urethra).
The shape of the cells in the surface layer of a transitional epithelium varies with the degree of distension of the organs whose lumen is lined by this type of epithelium. In the 'relaxed' state of the epithelium, it seems to be formed by many cell layers. The most basal cells have a cuboidal or columnar shape. There are several layers of polyhedral cells, and, finally, a layer of superficial cells, which have a convex, dome-shaped luminal surface. In the distended state of the epithelium only one or two layers of cuboidal cells are followed by a superficial layer of large, low cuboidal or squamous cells. In the distended state the epithelium will resemble a stratified squamous epithelium.
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Bladder, Monkey - H&E It has not yet been resolved if all
the epithelial cells are in contact with the basement membrane. Some texts
consider transitional epithelium as a specialised stratified epithelium
while others group it with pseudostratified epithelia. Maybe it is best
to also consider it 'transitional' in this regard. |
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Trachea, Human - H&E |
Basement membrane or basal lamina
Epithelia are separated from the underlying connective tissue by an extracellular
supporting layer called the basement membrane. The basement membrane is composed
of two sublayers. The basal lamina (about
80 nm thick) consists of fine protein filaments embedded in an amorphous
matrix. Membrane proteins of the epithelial cells are anchored in the basal lamina, which is also produced by the epithelial cells. The major components of the basal lamina are two glycoproteins - laminin and (usually type IV) collagen. The reticular
lamina consists of reticular fibres embedded in ground substance. The fibres of the reticular lamina connect the basal lamina with the underlying conective tissue. The
components of the reticular lamina are synthesised by cells of the connective
tissue underlying the epithelium.
In addition to its function as support of
the epithelium, the basal lamina acts as a selectively permeable filter between
epithelium and connective tissue.
Unless special stains are used, the basement membrane is rarely visible using light microscopy. You can read more about reticular fibres and ground substance on the Connective Tissues page.
Specialisations of the apical surface
Microvilli and stereocilia
are finger- or thread-shaped extensions of the epithelial cells. Their main
function is to increase the surface area of epithelial cells. They are typically
found in epithelia active in absorption. Microvilli contain actin filaments,
which are in contact with the terminal web of the cell
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The only difference between microvilli and stereocilia is their length. Microvilli
are much shorter than stereocilia. Stereocilia are, despite their name ("cilia"),
not actively moving structures.
Using light microscopy, stereocilia are difficult to discern from cilia.
Specialisations of the lateral and basal surfaces
Connective tissue is responsible for the structural integrity of most organs.
As mentioned above, it is absent from epithelia. Instead, tissue integrity as well as the barrier function of epithelia is taken care of by extensive cell-to-cell contacts between epithelial cells. These functions are mediated by several specialisations
in the lateral and basal parts of the cell membranes of the epithelial cells.
are specialisations of the lateral cell membranes which mediate cell adhesion.
Proteins inserted into the cell membrane of the adjacent cells form a protein-'zipper'
linking the cells. Fibers of the cytoskeleton attach to the cytoplasmic
side of the desmosome to stabilise the area of contact. Hemi-desmosomes
mediate the attachment of the epithelial cells to the basement membrane.
A group of glycoproteins (cadherins) inserted into
the opposing plasma membranes mediate cell-to-cell adhesion at desmosomes
and also at the adhesion zones or patches mentioned below. Integrins, another
group of proteins, allow the cell to attach to the matrix proteins of the
basal lamina.
are structurally not as well-characterised as desmosomes. An intermediate junction typically appears as a close and consistent apposition (15-20 nanometers) of the cell membranes near the apical cell surface. Intermediate junctions surround the entire cell. Again, fibres of the cytoskeleton insert into the cytoplasmic side of this membrane specialisation. Patches of adhesion resemble intermediate junctions structurally, but form more localized, patch- or strip-like contacts between neighbouring cells. They are found scattered over the lateral surfaces of the epithelial cell.
Proteins inserted into the cell membranes of adjacent cells 'stitch' the membranes of the cells together and provide an effective barrier to the diffusion of substances from the outside of the epithelium (called luminal side if the epithelium covers the surface of a tubular structure). Several "rows of stitches" may be found. Their number depends on the demand to reduce diffusion across the epithelium. Each of these rows reduces diffusion by about a factor 10 of what it was 'before'.
are cells or aggregations of cells whose function is secretion.
Both endocrine and exocrine glands are developmentally derived from epithelia, which form a down-growth into the underlying connective tissue. The cells forming this down-growth then develop the special characteristics of the mature gland. Exocrine glands maintain the connection with the surface epithelium, whereas the connection is lost by endocrine glands.
Exocrine glands may be classified according to cell number, and/or the shape and branching pattern of their secretory portions and ducts.
consist of a single secretory cell. In mammals the only example of unicellular exocrine glands are goblet cells, which occur in the epithelium of many mucous membranes. Goblet cells secrete the glycoprotein mucin, which by the uptake of water is converted into a slimy substance, mucus.
| Multicellular glands
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Combinations exist - the pancreas is a tubulo-acinar gland, in which each section
of the secretory system has a specialized function.
The precursors of digestive enzymes are produced by
the acinar cells. Tubular cells secrete the alkaline bicarbonate solution which
eventually neutralizes the acidic contents of the stomach that are released
into the duodenum.
Multicellular glands with an unbranched excretory duct are called simple. We talk about a compound gland when the excretory duct is branched. Finally, the part of the gland consisting of secretory cells is branched in a (surprise!) branched gland.
The classification scheme may appear somewhat elaborate - but there are many exocrine glands around. All of them can be identified and described by this scheme, and some ideas about their function can be derived from this description.
Colon, Human - van Gieson |
Exercise: Draw a compound branched tubulo-acinar gland. Indicate in your drawing which parts are secretory and which parts are non-secretory.
The secretory cells can release their secretory products by one of three mechanisms.
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There are two additional mechanisms by which secretory cells can release their products. Lipid soluble substances may diffuse out of the secretory cell (e.g. steroid hormone-producing endocrine cells). Transporters (membrane proteins) may actively move the secretory product across the plasma membrane (e.g. the acid producing parietal cells of the gastric glands). These secretory mechanisms may not involve any light microscopically visible specialisations of the cell.
The relationship between the secretory tissue (parenchyma) of glands and the supporting connective tissue is similar in most larger glands. Externally the entire gland is surrounded by a layer of dense connective tissue, the capsule. Connective tissue sheets (septa) extend from the capsule into the secretory tissue and subdivide the gland into a number of lobes. Thinner connective tissue septa subdivide the lobes into a number of lobules. Reticular connective tissue (hardly visible in H&E stained sections) surrounds and supports the secretory units of the glands (alveoli, acini etc.) and the initial parts of the excretory ducts if present.
Blood and lymph vessels as well as nerves penetrate the capsule and form a delicate network between the secretory units and the initial parts of the duct system.
The main excretory duct conveys the secretory product to one of the external surfaces of the body. Other parts of the duct system are named according to their relation to the lobes and lobules of the gland.
The appearance of the different portions of the duct system is quite variable from gland to gland and may allow the identification of the gland. Quite often, the appearance of parts of the duct system also permits some deductions about their functions.
? Note that lobes and lobules are defined by their relationship to each other. Many small lobules may form one large lobe. Neither size nor the spatial relationship between different parts of the tissue can be unequivocally determined in a single, two-dimensional section of the tissue. Lobes and interlobar ducts may therefore be difficult to distinguish from lobules and interlobular ducts.
Parotid Gland, Human - H&E |
Parotid Gland, Human and Sublingual
Gland, Human - H&E
Many secretory cells and the secretory structures formed by them belong to
one of two morphologically distinct forms: serous
or mucous. Serous secretions have a low viscosity,
i.e. they are rather "watery". Mucous secretions have a high viscosity, i.e.
they are rather "slimy". The apical cytoplasm of the cells forming serous
acini is usually well-stained. Secretory vesicles are visible in
the apical cytoplasm in well-preserve tissue. The nuclei are round or slightly
ovoid and located in the basal cytoplasm of the cells. The
bluish color of the basal cytoplasm reflects the presence of large amounts
of rough endoplasmatic reticulum.
The contents of the secretory vesicles in the apical cytoplasm of cells
forming mucous acini are only weakly stained. These
empty-looking vesicles give the apical cytoplasm of mucus-producing cells a
distinct "foamy" or "frothy" appearance. The nuclei of mucous cells appear darker
and smaller than the nuclei of serous cells. They also seem to be "pressed"
against the basal limit of the cells and may look flattened with an angular
("edgy") outline. Glands containing mucous acini (e.g.
the sublingual glands) are called mucous glands. Glands containing serous
acini (e.g. the parotid glands) are called serous
glands. If both types of acini are present the gland is muco-serous.
Identify and draw serous and mucous acini at high magnification.
Label your drawing. Make sure that the features which characterise serous and
mucous acini are visible in your drawing - if necessary
use a little artistic freedom.
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page content and construction: Lutz Slomianka
last updated:
1/10/06