Metachromasy

Metachromasia (var. metachromasy) is a characteristic change in the color of staining carried out in biological tissues, exhibited by certain dyes when they bind to particular substances present in these tissues, called chromotropes. For example, toluidine blue becomes dark blue (with a colour range from blue-red dependent on glycosaminoglycan content) when bound to cartilage. Other widely used metachromatic stains are the haematological Giemsa and May-Grunwald stains that also contain thiazine dyes. The white cell nucleus stains purple, basophil granules intense magenta, whilst the cytoplasms (of mononuclear cells) stains blue. The absence of color change in staining is named orthochromasia.

The underlying mechanism for metachromasia requires the presence of polyanions within the tissue. When these tissues are stained with a concentrated basic dye solution, such as toluidine blue, the bound dye molecules are close enough to form dimeric and polymeric aggregates. The light absorption spectra of these stacked dye aggregates differ from those of the individual monomeric dye molecules. Cell and tissue structures that have high concentrations of ionized sulfate and phosphate groups—such as the ground substance of cartilage, heparin-containing granules of mast cells, and rough endoplasmic reticulum of plasma cells—exhibit metachromasia. This depends on the charge density of the negative sulfate and carboxylate anions in the glycosaminoglycan (GAG). The GAG polyanion stabilizes the stacked, positively-charged dye molecules, resulting in a spectral shift as the conjugated double bond π-orbitals of adjacent dye molecules overlap. The greater the degree of stacking, the greater the metachromatic shift. Thus, hyaluronic acid, lacking sulphate groups and with only moderate charge density, causes slight metachromasia; chondroitin sulfate, with an additional sulfate residue per GAG saccharide dimer, is an effective metachromatic substrate, whilst heparin, with further N-sulfation, is strongly metachromatic. Therefore, toluidine blue will appear purple to red when it stains these components.

The metachromatic properties of dimethylmethylene blue, a thiazine dye closely related to toluidine blue, have been exploited to assay glycosaminoglycans extracted from cartilage and other connective tissues. The absorption peak shifts from about 630 nm (red absorption, therefore blue colour) to about 530 nm in the presence of GAG. Humbel and Etringer's original assay was developed by others to create a stable and widely used dimethylmethylene blue reagent.

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