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'Histology' (from the Greek '') is the study of tissue sectioned as a thin slice, using a microtome. It can be described as microscopic anatomy. The photographing of stained cells is called 'histography'. Histology is an essential tool of biology.
'Histopathology', the microscopic study of diseased tissue, is an important tool of anatomical pathology since accurate diagnosis of cancer and other diseases usually requires histopathological examination of samples.
The trained scientists who perform the preparation of histological sections are 'Histotechnicians', Histology Technicians (HT), Histology Technologists (HTL), Medical Scientists, Medical Laboratory Technicians or Biomedical scientists. Their field of study is called 'histotechnology'.

Contents

Source of tissue

Technical Procedure

Fixation

Processing

Embedding

Sectioning

Common Laboratory Stains

Alternative techniques

History

Histological classification of animal tissues

Related sciences

Artifacts

Pre-histology

Post-histology

References

See also

External links

Source of tissue

Histological examination of tissues starts with surgery, biopsy or autopsy (or necropsy, in the case of animal tissues). Engineered Tissue is also used for histological examination, some labs are able to use cells and engineer a tissue that would act as an equivalent to real tissue. The equivalent would not resemble real tissue, but would be a useful model for studying the interactions of cells with infection and many other conditions.

Technical Procedure

Fixation

Main articles: Fixation (histology)

The tissues are mechanically and biochemically stabilized in a fixative. The most common fixative is neutral buffered formalin (10% formaldehyde in Phosphate buffered saline (PBS)). A good fixative is when it is less toxic to the person handling it, and when it does not damage and harden the tissue being preserved.

Processing

The most common technique is wax processing. The samples are immersed in multiple baths of progressively more concentrated ethanol to dehydrate the tissue, followed by a clearing agent such as, xylene or Histoclear, and finally hot molten paraffin wax (impregnation). During this 12 to 16 hour process, paraffin wax will replace the xylene:

Embedding

Soft, moist tissues are turned into a hard paraffin block, which is then placed in a mold containing more molten wax (embedded) and allowed to cool and harden.
Embedding can also be accomplished using frozen, non-fixed tissue in a freezing medium. This freezing medium is liquid at room temperature but when cooled will solidify. Non-fixed tissue allows for procedures such as in-situ hybridizations for specific mRNA that would have been destroyed during the fixing process. It also allows for very short turnaround where that is needed, as with a patient currently undergoing surgery.

Sectioning

The tissue is then sectioned into very thin (2 - 8 micrometer) sections using a microtome. These slices, usually thinner than the average cell, are then placed on a glass slide for staining.
Frozen tissue embedded in a freezing medium is cut on a microtome in a cooled machine called a cryostat.
===Staining===
Routine staining:This is done to give contrast to the tissue being examined, as without staining it is very difficult to see differences in cell morphology. Hematoxylin and eosin (abbreviated H&E) are the most commonly used stains in histology and histopathology. Hematoxylin colors nuclei blue, eosin colors the cytoplasm pink.
To see the tissue under a microscope, the sections are stained with one or more pigments. Special Staining: There are hundreds of various other techniques which have been used to selectively stain cells and cellular components. Other compounds used to color tissue sections include safranin, oil red o, congo red, fast green FCF, silver salts and numerous natural and artificial dyes, that were usually originated from the development dyes for the textile industry.
Histochemistry refers to the science of using chemical reactions between laboratory chemicals and components within tissue. A commonly performed histochemical technique is the Perls Prussian blue reaction, used to demonstrate iron deposits in diseases like Hemochromatosis.
Histology samples have often been examined by radioactive techniques. In historadiography a slide (sometimes stained histochemically) is X-rayed. More commonly, autoradiography is used to visualize the locations to which a radioactive substance has been transported within the body, such as cells in S phase (undergoing DNA replication) which incorporate tritiated thymidine, or sites to which radiolabeled nucleic acid probes bind in in situ hybridization. For autoradiography on a microscopic level the slide is typically dipped into liquid nuclear tract emulsion, which dries to form the exposure film. Individual silver grains in the film are visualized with dark field microscopy.
Recently, antibodies are used to specifically visualize proteins, carbohydrates and lipids: this is called immunohistochemistry, or when the stain is a fluorescent molecule, immunofluorescence. This technique has greatly increased the ability to identify categories of cells under a microscope. Other advanced techniques can be combined with this, such as nonradioactive in situ hybridization to identify specific DNA or RNA molecules with fluorescent probes or tags that can be used for immunofluorescence and enzyme-linked fluorescence amplification (especially alkaline phosphatase and tyramide signal amplification). Fluorescence microscopy and confocal microscopy are used to detect fluorescent signals with good intracellular detail. Digital cameras are increasingly used to capture histological and histopathological images.

Common Laboratory Stains

Stain	Common use	Nucleus	Cytoplasm	Red Blood Cell (RBC)	Collagen Fibers	Specifically stains
Haematoxylin	General staining when paired with Eosin	Blue	N/A	N/A	N/A	Nucleic acids - Blueblue eER (ergastoplasm) - Blue
Eosin	General staining when paired with Haematoxylin	N/A	Pink	Orange/Red	Pink	Elastic fibers - pink,reticular fibers - pink
Toluidine blue	General staining	Blue	Blue	Blue	Blue	Mast cells granules - purple
Gomori's trichrome stain	Connective and muscle tissue	Gray/Blue	Red	Red	Green	Muscle Fibers - Red
Masson's trichrome stain	Connective tissue	Black	Red/Pink	Red	Blue/Green	Cartilage - Blue/green, Muscle fibers - Red
Mallory's trichrome stain	Connective tissue	Red	Pale Red	Orange	Deep Blue	Keratin - Orange,Cartilage - Blue, Bone matrix - Deep Blue, Muscle fibers - Red
Weigert's elastic stain	Elastic fibers	Blue/Black	N/A	N/A	N/A	Elastic fibers - Blue/Black
Heidenhains'azan trichrome stain	Distinguishing cells from extracellular components	Red/Purple	Pink	Red	Blue	Muscle fibers - RedCartilage - Blue, Bone matrix - Blue
Silver stain	Reticular fibers, Nerve fibers	N/A	N/A	N/A	Reticular fibers, Brown/BlackNerve Fibers - Brown/Black
Wright's stain	Blood cells	Bluish/Purple	Bluish/Gray	Red/Pink	N/A	Neutrophil granules - Purple/PinkEosinophil granules - Bright Red/OrangeBasophil granules - Deep Purple/VioletPlatelet granules - Red/Purple
Orcein stain	Elastic fibres	Deep Blue	N/A	Bright Red	Pink	Elastic fibres - Dark BrownMast cells granules - purpleSmooth Muscle - Light Blue
Periodic acid-Schiff stain (PAS)	Basement Membrane, Localising carbohydrates	Blue	N/A	N/A	Pink	Glycogen and other Carbohydrates - Magenta

Table sourced from Histology: A Text and Atlas, Michael H. Ross, Wojciech Pawlina,, , , Lippincott Williams & Wilkins, 2006,
The Nissl method and Golgi's method are useful in identifying neurons.

Alternative techniques

Alternative techniques include cryosection. The tissue is frozen and cut using a cryostat. Tissue staining methods are similar to those of wax sections. Plastic embedding is commonly used in the preparation of material for electron microscopy. Tissues are embedded in epoxy resin. Very thin sections (less than 0.1 micrometers) are cut using diamond or glass knives. The sections are stained with electron dense stains (uranium and lead) so that they can be seen with the electron microscope.

History

In the 19th century, histology was an academic discipline in its own right. The 1906 Nobel Prize in Physiology or Medicine was awarded to the histologists, Camillo Golgi and Santiago Ramon y Cajal. They had dueling interpretations of the neural structure of the brain based in differing interpretations of the same images.

Histological classification of animal tissues

There are four basic types of tissues: muscle tissue, nervous tissue, connective tissue, and epithelial tissue. All tissue types are subtypes of these four basic tissue types (for example blood cells are classified as connective tissue since they generally originate inside bone marrow).

★ Epithelium: the lining of glands, bowel, skin and some organs like the liver, lung, kidney,

★ Endothelium: the lining of blood and lymphatic vessels,

★ Mesothelium: the lining of pleural, and pericardial spaces,

★ Mesenchyme: the cells filling the spaces between the organs, including fat, muscle, bone, cartilage and tendon cells,

★ Blood cells: the red and white blood cells, including those found in lymph nodes and spleen,

★ Neurons: any of the conducting cells of the nervous system,

★ Germ cells: reproductive cells, spermatozoa in men, oocytes in women,

★ Placenta: an organ characteristic of true mammals during pregnancy, joining mother and offspring, providing endocrine secretion and selective exchange of soluble, but not particulate, blood borne substances through an apposition of uterine and trophoblastic vascularised parts, and

★ Stem cells: cells able to turn into one or several of the above types.
Note that tissues from plant, fungus and microorganisms can also be examined histologically. Their structure is very different from animal tissue.

Related sciences

★ Cell biology is the study of living cells, their DNA, RNA and the proteins they express.

★ Anatomy, is the study of organs visible by the naked eye; and

★ Morphology, which studies entire organisms.

Artifacts

See artifacts (Histology) for the main article and list of known histological artifacts
Artifacts are structures or features in tissue that interfere with normal histological examination. These are not always present in normal tissue and can come from outside sources. Artifacts interfere with histology by changing the tissues appearance and hiding structures. These can be divided into two categories:

Pre-histology

These are features and structures that have being introduced prior to the collection of the tissues. A common example of these include: ink from tattoos and freckles (melanin) in skin samples.

Post-histology

Artifacts can result from tissue processing. Processing commonly lead to changes like shrinkage, color changes in different tissues types and alterations of the structures in the tissue. Because these are caused in a laboratory the majority of post histology artifacts can be avoided or removed after being discovered. A common example is mercury pigment left behind after using Bouin's fixative to fix a section.

References

1. Merck Source (2002). Dorland's Medical Dictionary. Retrieved 2005-01-26.
2. Stedman's Medical Dictionaries (2005). Stedman's Online Medical Dictionary. Retrieved 2005-01-26.

See also

★ Pathology

★ Anatomical pathology

★ Histopathology

★ Biological staining

★ Important publications in histology

★ Geoffrey Bourne

External links

★ Histology Protocols

★ Immunohistochemistry - In Situ Hybridization

★ Histoweb

★ SIU SIM Histology

★ Visual Histology Atlas

★ Histology Glossary

★ Histology Group of Victoria Incorporated

★ Histology Photomicrographs