School of Anatomy and Human Biology - The University of Western Australia
Blue Histology - Connective Tissues
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School of Anatomy and Human Biology - The University of Western Australia | ||
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Blue Histology - Connective Tissues |
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Topics |
Lab Guides and Images |
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Reticular Fibres - liver, reticulin | |
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Elastic Fibres - artery, elastin & eosin | |
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Macrophages - liver, carbon injected, trichrome | |
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Mast Cells - tongue, toluidine blue | |
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Dense Regular Connective Tissue - tendon, van Gieson | |
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Dense Irregular Connective Tissue - non-lactating breast, H&E | |
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Adipose Tissue - kidney, trichrome and thick skin, H&E | |
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Mesenchymal Connective Tissue - umbilical cord, H&E |
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Connective tissue consists of cells separated by varying amounts of extracellular substance. In connective tissues cells typically account for only a small fraction of the tissue volume. The extracellular substance consists of fibres which are embedded in ground substance containing tissue fluid. Fibres in connective tissue can be divided into three types: collagen fibres, reticular fibres and elastic fibres.
Collagen fibres are the dominant fibre type in most connective tissues. The primary function of collagen fibres is to add strength to the connective tissue.
The thickness of the fibres varies from ~ 1 µm to 10 µm. Longitudinal striations may be visible in thicker fibres. These striations reveal that the fibres are composed of thinner collagen fibrils (0.2 to 0.5 µm in diameter). Each of these fibrils is composed of microfibrils, which are only visible using electron microscopy.
Microfibrils are assemblies of tropocollagen,
which, in turn, is an spiral-like assembly of three collagen molecules (triple
helix). The organisation of the tropocollagen within the microfibrils is highly
regular. A small gap (60 nm wide) is found between
the subsequent tropocollagens forming the microfibrils. Staining solutions used in electron microscopy tend to fill in
these gaps, and the alignment of the gaps gives the microfibrils a
cross-striated appearance (with 68 nm intervals) in
EM images
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Coarse collagen fibres are formed by type I tropocollagen.
There are many different tropocollagen types around (currently named type I to XX). These types differ in their content of the amino acids hydroxyproline and hydroxylysine. They also differ in the amount of carbohydrates attached to the collagen molecules. The different types of tropocollagen give the fibres the structural and functional features which are appropriate for the organ in which the fibres are found. Types I, II and III are the major fibre-forming tropocollagens. Tropocollagen type IV is an important structural component of the basal lamina.
A tensile force of several hundred kg/cm2 is necessary to tear or break human collagen fibres. The fibres stretch by only 15-20%.
Reticular fibres are very delicate and form fine networks instead of thick bundles. They are usually not visible in histological sections but can be demonstrated by using special stains. For example, in silver stained sections reticular fibres look like fine, black threads - coarse collagen fibres appear reddish brown in the same type of preparation.
Because of their different staining characteristics, reticular fibres were initially thought to be completely different from collagen fibres. Cross-striations with the same periodicity as in coarse collagen fibres are however visible using electron microscopy. We now know that reticular fibres consist of collagen - although the main type of tropocollagen found in reticular fibres, type III, is different from that of the coarse collagen fibres.
Reticular fibres give support to individual cells, for example, in muscle and adipose tissue.
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Liver - reticulin Blood will not be visible in some types of preparations and the sinusoids appear empty. |
Elastic fibres are coloured in fresh tissues - they are light yellow - but
this colouration is only visible if large amounts of elastic fibres are present
in the tissue, for example, in the elastic ligaments of the vertebral column.
Special stains are necessary to show elastic fibres in tissue sections.
R esorcin fuchsin is one of these stains, which gives the
elastic fibres a dark violet colour.
Light microscopy does not reveal any substructure in the elastic fibres. Electron microscopy shows that elastic fibres consist of individual microfibrils, which are embedded in an amorphous matrix. The matrix accounts for about 90% of the fibre and is composed of the protein elastin. Neither the elastin nor the microfibrils are collagens.
Elastic fibres can be stretched to about 150% of their original length. They resume their original length if the tensile forces applied to the elastic fibres are relaxed.
Elastin is a somewhat odd protein in that its amino acid sequence does not determine a specific three-dimensional structure of the molecule. Instead, elastin remains unfolded as a "random coil". Elastin molecules are cross-linked to each other by desmosin and isodesmosin links, which are only found between elastin molecules. Tensile forces straighten the cross-linked mesh of elastin coils.
Artery, human - elastin & eosin
Like
reticular fibres, elastic fibres require special stains to be visualized.
Typically elastic fibres will appear as fine, dark violet and gently undulating
fibres in the tissue. Elastic fibres can form membranes - not unlike the
collagen membrane in the basal lamina of epithelia. This is the case at some
levels in the walls of blood vessels.
A combination
with a second stain is necessary to visualize other tissue components. Colours
visible in the sections will depend on the method used in combination with the
elastin stain. Eosin gives an even pink or red colour to many tissue components.
Nuclei of cells remain unstained without the inclusion of the haematoxylin in
the staining solutions.
Identify the artery and the vein in the section.
Their walls contain large amounts of elastic fibres. Which one contains more
elastic fibres - artery or vein?
Draw a small
section of the wall of a vessel, preferably an artery, at high magnification.
Identify elastic laminae, fine and coarse elastic fibres in your drawing.
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Ground substance is found in all cavities and clefts between the fibres and
cells of connective tissues. Water, salts and other low molecular substances are
contained within the ground substance, but its main structural constituent are
proteoglycans.
Ground substance is soluble in most of
the solvents used to prepare histological sections and therefore not visible in
ordinary sections.
Proteoglycans are responsible for the highly viscous character of the ground substance. Proteoglycans consist of proteins (~5%) and polysaccharide chains (~95%), which are covalently linked to each other. The polysaccharide chains belong to one of the five types of glycosaminoglycans, which form the bulk of the polysaccharides in the ground substance.
Hyaluronan (or hyaluronic acid) is the dominant glycosaminoglycan in connective tissues. The molecular weight (MW) of hyaluronic acid is very high (~ MW 1,000,000 ). With a length of about 2.5 µm hyaluronan is very large. Hyaluronan serves as a "backbone" for the assembly of other glycosaminoglycans in connective and skeletal tissue, which results in even larger molecule complexes (MW 30,000,000 - 200,000,000). Hyaluronan is a major component of the synovial fluid and the vitreous body of the eye.
The remaining four major glycosaminoglycans are chondroitin sulfate, dermatan sulfate, keratan sulfate and heparan sulfate. These glycosaminoglycans attach via core- and link-proteins to a backbone formed by the hyaluronic acid. The coiled arrangement of the hyaluronan and other attached glucosaminoglycans fills a roughly spherical space with a diameter of ~0.5 µm. This space is called a domain. Neighbouring domains overlap and form a more or less continuous three-dimensional molecular sieve in the interstitial spaces of the connective tissues.
The large polyanionic carbohydrates of the glycosaminoglycans bind large amounts of water and cations. The bound water in the domains forms a medium for the diffusion of substances of low molecular weight such as gases, ions and small molecules, which can take the shortest route, for example, from capillaries to connective tissue cells. Large molecules are excluded from the domains and have to find their way through the spaces between domains.
The restricted motility of larger molecules in the extracellular space inhibits the spread of microorganisms through the extracellular space. A typical bacterium ( 0.5 x 1 µm) is essentially immobilised in the meshwork formed by the domains. The pathogenicity of a bacterium is indeed to some extent determined by its ability to find its way through the mesh, and some of the more invasive types produce the enzyme hyaluronidase, which depolymerises hyaluronic acid.
Components of the ground substance, collagen and reticular fibres are synthesised by cells of the connective tissues, the fibrocytes. Elastic fibres are synthesised by both fibrocytes and smooth muscle cells.
Connective tissue cells are usually divided into two groups based on their ability to move within the connective tissue. Fibrocytes (or fibroblasts) and fat cells are fixed cells. Macrophages, monocytes, lymphocytes, plasma cells, eosinophils and mast cells are wandering cells.
Fibrocytes are the most common cell type in connective tissues. They are the "true" connective tissue cells. Usually only their oval, sometimes flattened nuclei are visible in LM sections. The cytoplasm of a resting (i.e. inactive) fibrocyte does not contain many organelles. This situation changes if the fibrocytes are stimulated, for example, by damage to the surrounding tissue. In this case the fibrocyte is transformed into a fibroblast, which contains large amounts of the organelles which are necessary for the synthesis and excretion of proteins needed to repair the tissue damage (Which ones?). Fibrocytes do not usually leave the connective tissue. They are, however, able to perform amoeboid movement.
The terms fibrocyte and fibroblast refer here to the inactive and active cells respectively - at times you will see the two terms used as synonyms without regard for the state of activity of the cell.
Reticular cells are usually larger than an average fibrocyte. They are the "fibrocytes" of reticular connective tissue and form a network of reticular fibres, for example, in the lymphoid organs. Their nuclei are typically large and lightly stained (H&E) and the cytoplasm may be visible amongst the cells which are housed within the network of reticular fibres.
Fat cells or adipocytes are fixed cells in loose connective tissue. Their main function is (what surprise!) the storage of lipids. If "well fed" the cytoplasm only forms a very narrow rim around a large central lipid droplet. The flattened nucleus may be found in a slightly thickened part of this cytoplasmic rim - if it is present in the section, which may not be the case since the diameter of an adipocyte (up to 100 µm) is considerable larger than the thickness of typical histological sections. A "starving" adipocyte may contain multiple small lipid droplets and gradually comes to resemble a fibrocyte.
Lipid storage/mobilisation is under nervous (sympathetic) and hormonal (insulin) control. Adipocytes also have an endocrine function - they secrete the protein leptin which provides brain centers which regulate appetite with feedback about the bodies fat reserves.
Leptin deficiency in experimental animals results in obesity.Adipocytes are very long-lived cells. Their number is determined by the number of preadipocytes (or lipoblast) generated during foetal and early postnatal development.
Macrophages
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Liver, rabbit - carbon injected,
trichrome Macrophages found in the liver are also called Kupffer cells. They adhere to the epithelial lining of the liver sinusoids, i.e. blood filled spaces between the liver cells. Blood will not be visible in some types of preparations and the sinusoids appear empty. Once you have identified macrophages, go hunting for some good collagen - in trichrome stains the collagen fibres will often appear green(ish). Typically you will see them only in the connective tissue surrounding larger blood vessels. Improve your knowledge on epithelia and look out for ducts lined by a simple cuboidal or columnar epithelium. What is flowing in these ducts? |
Mast cells are - like macrophages, lymphocytes and eosinophils - in demand when something goes wrong in the connective tissue. Quite a few of them are present in healthy connective tissue as they stand on guard and monitor the local situation. The cytoplasm of mast cells is filled by numerous large vesicles. Mast cells discharge the contents of these vesicles if they come in contact with antigens, for example, proteins on the surface of an invading bacterium or, in allergic reactions, in response to antigens found, for example, on the surface of pollen grains.
The most prominent substances contained in the vesicles are heparin and histamine. They increase blood flow in close by vessels and the permeability of the vessel walls to plasma constituents and other white blood cells. By facilitating access to the area, mast cells facilitate an immune response to the antigen which triggered the release histamine and heparin.
Other connective tissue cells
Lymphocytes and plasma cells
Lymphocytes are usually small cells (6 - 8 µm). Their nuclei are round and stain very dark. The cytoplasm forms a narrow rim around the nucleus and may be difficult to see. There are many of them in the connective tissue underlying the epithelia of the gastrointestinal tract but usually much fewer in other connective tissues. Again, this situation may change - in this case with immunological reactions. Some lymphocytes may differentiate into plasma cells. Plasma cells are lymphocytes which produce antibodies. To accommodate the necessary organelles for this function the size of the cytoplasm increases dramatically and the cells become basophilic. Plasma cells can occasionally be spotted in the loose connective tissue present in sections.
Like eosinophilic cells and monocytes, lymphocytes are white blood cells. More information about these cell types can be found on the "Blood" page.
Eosinophilic cells
Eosinophilic cells are typically rounded or oval, large cells, which contain large amounts of bright red granules in their cytoplasm. They originate, like the monocytes, in the bone marrow. They enter connective tissues early in inflammatory reactions, where they phagocytose antigen-antibody complexes. Their numbers in healthy connective tissue vary with location, but a few of them can usually be found.
Mesenchymal cells
During development, mesenchymal cells give rise to other cell types of the connective tissue. A small number of them may persist into adulthood. Mesenchymal cells are smaller than fibrocytes and difficult to detect in histological sections. They may regenerate blood vessels or smooth muscle which have been lost as a consequence of tissue damage.
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Tongue, Mast Cells - toluidine blue |
These two tissues are distinguished according to the relative amounts of fibres they contain. Dense connective tissues are completely dominated by fibres. They are subdivided according to the spatial arrangement of the fibres in the tissue.
In dense irregular connective tissue the fibres do not show a clear orientation within the tissue but instead form a densely woven three-dimensional network. A good example is the dermis of the skin.
We talk about regular dense connective tissue if the fibres run parallel to each other. Good examples of regular dense connective tissue are tendons, ligaments and the fasciae and aponeuroses of muscles.
Loose connective tissue is relatively cell rich, soft and compliant. It is also rich in vessels and nerves. It is best understood as a kind of generalised connective tissue in which all connective tissue cell types may occur. Loose connective tissue may occur in some special variants: mucous connective tissue, reticular connective tissue and adipose tissue.
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Muscle-Tendon Junction, rat - van
Gieson |
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Non-lactating Breast - H&E The excretory ducts of the mammary glands are called
lactiferous ducts. They are lined by a quite nice stratified columnar
epithelium. If you are working with a section of non-lactating breast look
for the lactiferous ducts in the connective tissue. |
Reticular connective tissue consists of reticular cells and the network of reticular fibres formed by them. Most connective tissues contain reticular fibres, but only in reticular connective tissue are they the dominant fibre type. In a number of tissues and organs, reticular connective tissue forms the structural framework in which the cells of the organ are suspended. The open meshwork of fine fibres is particularly useful in tissues and organs in which diffusion and / or cell movements are functionally important, for example, in the liver, lymph nodes and the spleen.
Adipose tissue is essentially loose connective tissue containing large numbers of adipocytes. There are two types of adipose tissue, which derive their names from the colour of the tissue (white or brown) and/or the number of lipid droplets found in the adipocytes.
