Histology, M Cell

Structure

M cells differ structurally from normal intestinal mucosal cells. M cells have apical microfolds, hence their alternate name, "microfold cells." These apical microfolds are poorly organized villi that have unique adhesion molecules to grab and sample luminal macromolecules. They have a thin glycocalyx, as opposed to the normally thick glycocalyx of other mucosal epithelial cells, that allows for adhesion but also does not impend the transport of molecules.[1][2] They have a unique intraepithelial invagination, or "pocket," on the basolateral surface that can also be seen via electron microscopy. These invaginations allow macrophages and other immune cells to process the engulfed macromolecules in a short time, decreasing the time from transport to processing.[1][3]

Function

M cells function as sentries against intestinal toxins and/or pathogens, transporting them (trans-epithelial) to awaiting immune cells. M cells specialize in transcytosis (ie, trans-epithelial transport). M cells uptake macromolecules (antigens, pathogens) from their apical surface (intestinal luminal surface) and transport these molecules, via vesicles, to the basolateral surface. This transport appears to be non-selective; however, some specialized adhesion and transport markers have been noted, such as in the case of Vibrio uptake. There also are several basolateral invaginations which house macrophages and other immune cells. These immune cells process the presented molecules and deliver them further onto intestinal lymphoid follicles to initiate an immune response.[4][5][6] This function has been known to be exploited as a method to gain entry into the body past the intestinal epithelial barrier.

Tissue Preparation

These cells lack typical enterocyte glycoproteins, mainly alkaline phosphatase and sucrase-isomaltase. These are used as negative markers for the identification of M cells. Due to their shortened, irregular microvilli, M cells also stain poorly for actin, villi, and other microvilli-associated proteins. This lack of villous staining can be further used to identify M cells.[1]

Histochemistry and Cytochemistry

Specific glycosylation patterns and lectins appear to vary among M cells, although some lectins have been used to characterize M cells. The ulex europaeus agglutinin-1 and winged bean basic agglutinin lectins have been used to stain specifically for M cells, though it is not clear how commonly these lectins are involved with M cells.[1] M cells arise from LGLgr5 stem cells found in the intestinal crypts. RANKL expression, among various tumor necrosis factors and other cytokines, is needed to signal the development of M cells from the stem cells mentioned above. Deletions or functional modifications of RANKL have been linked to M cell deficiency.[7][8][9]

Microscopy, Light

On light microscopy, M cells can be seen to have an absence of thick microvilli on their apical (luminal) surface and "pockets" of immune cells within their basolateral borders. Otherwise, electron microscopy and/or immunochemistry are used to identify these cells.[1]

Microscopy, Electron

M cells have apical microfolds on electron microscopy (hence their alternate name, "microfold cells"). These apical microfolds are poorly organized villi that have unique adhesion molecules to grab and sample luminal macromolecules. They have a unique intraepithelial invagination (or "pocket") on the basolateral surface can also be seen via electron microscopy. These invaginations allow for macrophages and other immune cells to process the engulfed macromolecules.[1]

Clinical Significance

M cells are important for maintaining mucosal immunity function, particularly in the intestines. The immunologic reaction to many common intestinal pathogens, such as various Vibrio species, depends on initial uptake by M cells.[1][10] It has been noted that in aged mice, there is a decrease in M cells along the intestinal epithelial border, possibly playing a role in age-related immune dysfunction.[7][11] M cell damage has also been implicated in intestinal inflammation, where damaged M cells allow for unregulated uptake of inflammatory molecules/pathogens into the sub-epithelial space, potentiating the inflammatory process.[12] M-cell deficiency, leading to immunodeficiencies, is noted in cases of RANKL deletion/modification due to its role in M cell development.[8]

Numerous intestinal pathogens also exploit the function of M cells to gain entry into the sub-epithelium, notable ones being Shigella and Listeria. Salmonella has been noted to target and destroy M cells to both gain further entry into sub-epithelial tissues and avoid immunologic processing. Yersinia intestinal infections appear to use M cells as their primary method of entry into lymphoid follicles. Human immunodeficiency virus appears to use M cells as a method to spread and infect T cells based in mucosal lymphoid tissues.[1][4][13] M cells are being explored as vaccine and drug routes. Mucosal administration of many drugs and vaccines is often cheaper and safer than other methods. This route of administration also has the added benefit of engaging both the mucosal and systemic immune responses. Several studies have shown an ability to use M cells specifically to administer vaccines/drugs; however, the exact role efficiency of this method is still being explored.[14][15][16]