4.3 Article

Lactoferrin and the development of salivary stones: a pilot study

Journal

BIOMETALS
Volume 36, Issue 3, Pages 657-665

Publisher

SPRINGER
DOI: 10.1007/s10534-022-00465-7

Keywords

Sialolith; Salivary stone; Protein composition; Lactoferrin; Lysozyme

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Salivary stones are calcified structures in the ductal system of salivary glands. The study analyzed the protein composition of submandibular sialoliths and found that proteins, including alpha-amylase, lysozyme, lactoferrin, secretory-IgA, etc., contribute to the formation of sialoliths. The increasing size of a sialolith may cause local inflammation, and lactoferrin may play a new pathophysiological role in the process.
Salivary stones (sialoliths) are calcified structures located in the ductal system of the major salivary glands. Their exact cause is not clear but in general they are characterized by concentric inorganic (hydroxyapatite) layers. The formation is a slow intermittent process which may result in enlargement of the sialolith causing obstruction of saliva secretion resulting in mealtime related pain and swelling of the affected salivary gland. Various studies reported the presence of organic material such as proteins and lipids in the core of sialoliths. In the present study the protein composition of twenty submandibular sialoliths was analyzed. It was found that proteins contributed on average 5% to the dry weight of submandibular stones whereby small salivary stones contained more extractable proteins than large salivary stones. Using a combination of SDS-PAGE gel electrophoresis and Western blotting, we identified alpha-amylase (in all stones; 100%), lysozyme (95%), lactoferrin (85%), secretory-IgA (75%), MUC7 (60%), complement C4 (60%) and C-reactive protein (35%). The presence, and the combinations, of lactoferrin, lysozyme, s-IgA and alpha-amylase in sialoliths was confirmed by ELISA. The gradually increasing size of a sialolith might provoke a local inflammatory response in the duct of the submandibular gland whereby the relatively low concentrations of lactoferrin and lysozyme may originate from neutrophils. The interaction of lactoferrin with s-IgA could contribute to the accumulation of lactoferrin in sialoliths. In summary, these results suggest a new pathophysiological role for lactoferrin, in the formation of sialoliths.

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