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Preparation of histology slides involves several processes including staining sections of biological tissue after they have been mounted onto slides.
Not sure what histology is ?
See definition of Histology and definition of Histopathology

How to Prepare Histology Slides

How to prepare histology slides is not usually knowledge required for first-level courses in Anatomy & Physiology (e.g. ITEC) and Human Biology (e.g. A-Level in UK). It is, however, useful to have a general awareness of the steps involved in preparing histology slides.

It may be useful for school and college students to know a bit about how to prepare histology slides as part of their general appreciation of laboratory biology and techniques used in medical research. Familiarity with terminology used in the discipline of histology is also useful when reading around the subject or communicating with other professionals working in various fields within health sciences e.g. during work experience.

The five main stages in the preparation of histology slides are:

    1. Fixing
    2. Processing
    3. Embedding
    4. Sectioning
    5. Staining

Each of these stages is described briefly, as follows:

  • Fixing

Samples of biological tissue are "fixed" to preserve the cells/tissue in as natural a state as possible and prevent postmortem decay (autolysis and putrefaction). Chemical fixatives are very carefully selected substances whose properties must meet many criteria. Even the most careful fixation alters the sample to a certain extent and may potentially introduce artifacts that can interfere with interpretation of images of the fine detail of cells, incl. all their organelles, that can only be observed using an electron microscope (such fine detail of cells that can only be seen using electron microscopes is called "cellular ultrastructure").
Part of the skill involved in preparing and interpreting histology slides is in maintaining the structure of the sample in as undisturbed a state and possible, minimising the introduction of artifacts and recognising artifacts as such when they are present. Because fixation is usually the first stage in a multistep process to prepare biological material for microscopy or other analysis, the choice of fixation method and specific fixative may depend on the subsequent processing steps appropriate in that particular case.

Chemical Fixation.
In this case biological structures are preserved (both chemically and structurally) in a state as close to that of the living tissue as possible. This requires a chemical fixative that can stabilise the proteins, nucleic acids and mucosubstances of the tissue by making them insoluble.

Frozen Sections
Small pieces of tissue (typically 5mm x 5mm x 3 mm) are placed in a cryoprotective embedding medium then snap frozen in isopentane (an alkane) cooled by liquid nitrogen. Tissue is then sectioned in a freezing microtome or cryostat. Sections are then fixed by immersion in a specific fixative or series of fixatives for carefully controlled period of time.

Advantages - of fixation by frozen sections

Disadvantages - of fixation by frozen sections

  • Give better preservation of antigenicity
  • Minimal exposure to fixative
  • Not exposed to the organic solvents
  • Lack morphological detail
  • Possibility of biohazard
  • Processing

Tissue processing is done to remove water from the biological tissues, replacing such water with a medium that solidifies, setting very hard and so allowing extremely thin sections to be sliced. This is important because biological tissue must be supported in an extremely hard solid matrix to enable sufficiently thin sections to be cut. Some typical values are:

5 μm thick for light microscopy
5 μm (i.e. 5 micrometres) = 0.005 mm = 0.000005 metre

80-100 nm thick for electron microscopy
80-100 nm (i.e. 80-100 nanometres) = 0.00008 mm to 0.0001 mm = 0.00000008 to 0.0000001 metre

See the page about Scientific Numbers for more about these units.

Removal of water is also referred to as "dehydration".

  • Embedding

After tissues have been dehydrated and before they can be "sectioned" i.e. sliced very thinly (see the thicknesses mentioned above) they must be secured in a very hard solid block in such a way that the hardened material used to secure all parts of the biological tissues in place is transparent to the optical method used for viewing the finished samples.

Different types of embedding techniques and materials are used depending on the sample being prepared and the other types of processing involved in preparing that particular sample.

In general, tissue samples are placed in molds together with liquid embedding material which is then hardened. The result of this stage in the preparation of histology slides is hardened blocks containing the original biological samples together with other substances used so far in the preparation process.

  • Sectioning

Sectioning an embedded tissue sample is the step necessary to produce sufficiently thin slices of sample that the detail of the microstructure of the cells/tissue can be clearly observed using microscopy techniques (either light microscopy or electron microscopy).

Possible orientations at which tissue samples may be sectioned include:

  • Vertical sectioning perpendicular (i.e. at right-angles) to the surface of the tissue.
    This is the most common method.
  • Horizontal sectioning is often done for the study of hair follicles and structures that include hairs, hair follicles, arrector pili muscles, and sebaceous glands in general. Such structures are sometimes called "pilosebaceous units".
  • Tangential to horizontal sectioning is done in chemosurgery (also called "Mohs surgery") which is a form of microscopically controlled surgery used to treat certain types of skin cancer.

The method used to actually cut sections from the hardened block of tissue depends on the type of microscopy that will be used to observe it and hence the thickness of sample required. In the case of samples to be studied using light microscopy, a steel knife mounted in a microtome may be used to cut 10μm tissue sections which are then mounted on a glass microscope slide. In the case of samples to be studied using transmission electron microscopy, a diamond knife mounted in an ultramicrotome may be used to cut 50 nm tissue sections which are then mounted on a 3-millimeter-diameter copper grid.

  • Staining

Finally, the mounted sections are treated with an appropriate histology stain.

Why are histology samples stained ?
Put another way, what is the purpose of histology stains ?

Biological tissue has very little variation in colours/shades when viewed using either an ordinary light (optical) microscope or an electron microscope. Staining biological tissues is done to both increase the contrast of the tissue and also highlight some specific features of interest - depending on the type of tissue and the stain used.

There are many different histology stains. Histology stains are normally selected according to the type of tissue to be observed. Some stains are more widely used than others while some are only used to study very specific types of biological tissue.
To continue reading about this topic go on to the page about Histology Stains.

For more information see also pages about What is Histology, Histology Stains, Histopathology and the Structure of a Cell.
The report Differential Staining With Acid Dyes* may also be of interest. *Copyright Bryan D. Llewellyn.
Made available for download from this website for educational purposes within conditions of use stipulating that the text is unchanged and no charge is made. Accessed by us from http://stainsfile.info/StainsFile/downloads.htm

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