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Variations in lectin binding properties of intestinal M cells
M A Jepson1, C M Mason, M A Clark
1Department of Physiological Sciences, University of Newcastle upon Tyne, Medical School, UK.
Journal of Drug Targeting
|January 1, 1995
Summary
Lectins reveal distinct M cell surface glycoconjugates in Peyer's patches and caecal patches across species. This variation impacts antigen sampling and M cell-targeted delivery strategies.
Area of Science:
- Immunology
- Glycobiology
- Gastroenterology
Background:
- Follicle-associated epithelia (FAE) contain specialized M cells crucial for immune surveillance.
- Understanding M cell surface characteristics is vital for antigen uptake and targeted drug delivery.
- Glycoconjugate expression on M cells varies significantly between species and anatomical locations.
Purpose of the Study:
- To investigate and compare glycoconjugate expression on M cells in murine and rabbit Peyer's patches and caecal patches.
- To identify specific lectin binding patterns indicative of M cell surface glycoconjugates.
- To assess the implications of observed variations for M cell function and targeted delivery.
Main Methods:
- Application of a panel of lectins to fixed, whole tissue preparations of mouse and rabbit Peyer's and caecal patches.
- Selective binding of alpha-L-fucose-specific lectins (e.g., Ulex europaeus agglutinin I) to murine Peyer's patch M cells.
- Differential lectin binding patterns observed in rabbit caecal patch M cells and Peyer's patch enterocytes.
Main Results:
- Ulex europaeus agglutinin I selectively bound to M cells in murine Peyer's patches but not in mouse caecal patches.
- Ulex europaeus agglutinin I, wheat germ agglutinin, peanut agglutinin, and Bandeiraea simplicifolia agglutinin II showed selective binding to rabbit caecal patch M cells.
- Distinct lectin binding profiles highlight significant regional and species-specific differences in M cell surface glycoconjugates.
Conclusions:
- M cell surface glycoconjugate expression exhibits marked regional and species variation.
- These variations influence the normal antigen-sampling function of M cells.
- Findings provide insights for the rational design of particulates for transepithelial delivery via the M cell portal.