Periodic acid–Schiff stain
Periodic acid–Schiff (PAS) is a staining method used to detect polysaccharides such as glycogen, and mucosubstances such as glycoproteins, glycolipids and mucins in tissues. The reaction of periodic acid oxidizes the vicinal diols in these sugars, usually breaking up the bond between two adjacent carbons not involved in the glycosidic linkage or ring closure in the ring of the monosaccharide units that are parts of the long polysaccharides, and creating a pair of aldehydes at the two free tips of each broken monosaccharide ring. The oxidation condition has to be sufficiently regulated so as to not oxidize the aldehydes further. These aldehydes then react with the Schiff reagent to give a purple-magenta color. A suitable basic stain is often used as a counterstain.
PAS diastase stain (PAS-D) is PAS stain used in combination with diastase, an enzyme that breaks down glycogen. Alcian blue/periodic acid–Schiff (AB/PAS or AB-PAS) uses alcian blue before the PAS step.
PAS staining is mainly used for staining structures containing a high proportion of carbohydrate macromolecules (glycogen, glycoprotein, proteoglycans), typically found in e.g. connective tissues, mucus, the glycocalyx, and basal laminae.
PAS staining can be used to assist in the diagnosis of several medical conditions:
- Glycogen storage disease (versus other storage disorders);
- Adenocarcinomas, which often secrete neutral mucins;
- Paget disease of the breast;
- Alveolar soft part sarcoma;
- staining macrophages in Whipple's disease;
- It can be used to diagnose α1-antitrypsin deficiency if periportal liver hepatocytes stain positive;
- aggregates of PAS positive lymphocytes are present in epidermis in Mycosis fungoides and Sezary syndrome, called Pautrier microabscesses;
- erythroleukemia, a leukemia of immature red blood cells. These cells stain a bright fuchsia.;[not in citation given]
- Pulmonary alveolar proteinosis;
- Fungal infection, the cell walls of fungi stain magenta. This only works on living fungi; in contrast, Grocott's methenamine silver stain(GMS) will stain both living and dead fungal organisms.
- It is used to identify glycogen in lung biopsy specimens of infants with pulmonary interstitial glycogenosis (PIG)
- It can be use to highlight super cross-linked lipids inclusions in ceroid lipofuscinosis (NCL)
Presence of glycogen can be confirmed on a section of tissue by using diastase to digest the glycogen from a section, then comparing a diastase digested PAS section with a normal PAS section. The diastase negative slide will show a magenta staining where glycogen is present within a section of tissue. The slide that has been treated with diastase will lack any positive PAS staining in those locations on the slide
PAS staining is also used for staining cellulose. One example would be looking for implanted medical devices composed of nonoxidized cellulose.
If the PAS stain will be performed on tissue, the recommended fixative is 10% neutral-buffered formalin or Bouin solution. For blood smears, the recommended fixative is methanol. Glutaraldehyde is not recommended because free aldehyde groups may be available to react with the Schiff reagent, which may result in false positive staining.
- Methyl violet
- Prussian blue
- Egyptian Blue
- Methyl blue
- Methylene blue
- New methylene blue
- Han Purple
- Potassium ferrocyanide
- Potassium ferricyanide
- Gentian violet
- Fluorescein isothiocyanate (FITC)
- Fluorescein amidite (FAM)
- Rose Bengal
- DyLight Fluor, a product line of fluorescent dyes
- Fluorescein diacetate hydrolysis, a biochemistry laboratory test
- Laser dyes
- Thomas J. Lawton (27 April 2009). Breast. Cambridge University Press. pp. 55–. ISBN 978-0-521-88159-3. Retrieved 16 November 2010.
- (Ladanyi et al 2002
- C. Hauser (29 August 2005). Mayo Clinic Gastroenterology and Hepatology Board Review. CRC Press. pp. 108–. ISBN 978-0-203-50274-7. Retrieved 16 November 2010.
- Carson, Freida L.; Hladik, Christa (2009). Histotechnology: A Self-Instructional Text (3 ed.). Hong Kong: American Society for Clinical Pathology Press. pp. 137–139. ISBN 978-0-89189-581-7.