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Updated: Aug 14, 2026

Gene Expression Analyses in Human Follicles
Published on: February 17, 2023
Distinct gene expression profiles characterize cellular phenotypes of follicle-associated epithelium and M cells
Koji Hase1, Sayaka Ohshima, Kazuya Kawano
1Laboratory of Epithelial Immunobiology, Research Center for Allergy and Immunology, RIKEN Yokohama, Kanagawa, Japan.
Abstract:
Follicle-associated epithelium (FAE) covering Peyer's patches contains specialized epithelial M cells that take up ingested macromolecules and microorganisms from the lumen of the gut by transcytosis. Using high-density oligonucleotide microarrays, we analyzed the gene expression profiles of FAE and M cells in order to characterize their cellular phenotypes. The microarray data revealed that, among approximately 14,000 genes, 409 were expressed in FAE at twofold or higher levels compared to the intestinal epithelial cells (IECs) of the villi. These included genes involved in membrane traffic, host defense and transcriptional regulation, as well as uncharacterized genes. Real-time PCR and in situ hybridization analyses identified three molecules, ubiquitin D (Ub-D), tumor necrosis factor receptor superfamily 12a (TNFRsf12a), and transmembrane 4 superfamily 4 (Tm4sf4), which were predominantly distributed throughout FAE, but were expressed little, if at all, in IECs. By contrast, transcripts of secretory granule neuroendocrine protein 1 (Sgne-1) were scattered in FAE, and were co-localized with Ulex europaeus agglutinin-1 (UEA-1)-positive cells. This clearly suggests that expression of Sgne-1 in the gut is specific to M cells. Such a unique pattern of gene expression distinguishes FAE and M cells from IECs, and may reflect their cellular phenotype(s) associated with specific functional features.
Insights
Specialized M cells in the gut
Area of Science:
- Immunology
- Gastroenterology
- Molecular Biology
Background:
- Follicle-associated epithelium (FAE) in Peyer's patches contains M cells.
- M cells transport gut antigens via transcytosis.
Purpose of the Study:
- To characterize the cellular phenotypes of FAE and M cells.
- To identify genes specific to FAE and M cells.
Main Methods:
- High-density oligonucleotide microarrays for gene expression profiling.
- Real-time PCR and in situ hybridization for validation.
Main Results:
- 409 genes showed higher expression in FAE compared to intestinal epithelial cells (IECs).
- Ubiquitin D, TNFRsf12a, and Tm4sf4 were predominantly in FAE.
- Secretory granule neuroendocrine protein 1 (Sgne-1) expression was specific to M cells.
Conclusions:
- FAE and M cells exhibit a unique gene expression profile distinct from IECs.
- This profile reflects specialized functions in antigen sampling and immune response.
- Sgne-1 serves as a potential M cell-specific marker.
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