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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Kanaya, Takashi Miyazawa, Kohtaro Takakura, Ikuro Itani, Wataru Watanabe, Kouichi Ohwada, Shyuichi Kitazawa, Haruki Rose, Michael T. McConochie, Huw R. Okano, Hideyuki Yamaguchi, Takahiro Aso, Hisashi |
| Description | Country affiliation: Japan Author Affiliation: Kanaya T ( Cellular Biology Laboratory, Graduate School of Agricultural Science, Tohoku Univ., 1-1 Tsutsumidori Amamiyamachi, Aoba-ku, 981-8555 Sendai, Japan.) |
| Abstract | M cells are a kind of intestinal epithelial cell in the follicle-associated epithelium of Peyer's patches. These cells can transport antigens and microorganisms into underlying lymphoid tissues. Despite the important role of M cells in mucosal immune responses, the origin and mechanisms of differentiation as well as cell death of M cells remain unclear. To clarify the mechanism of M cell differentiation, we established a novel murine intestinal epithelial cell line (MIE) from the C57BL/6 mouse. MIE cells grow rapidly and have a cobblestone morphology, which is a typical feature of intestinal epithelial cells. Additionally, they express cytokeratin, villin, cell-cell junctional proteins, and alkaline phosphatase activity and can form microvilli. Their expression of Musashi-1 antigen indicates that they may be close to intestinal stem cells or transit-amplifying cells. MIE cells are able to differentiate into the M cell lineage following coculture with intestinal lymphocytes, but not with Peyer's patch lymphocytes (PPL). However, PPL costimulated with anti-CD3/CD28 MAbs caused MIE cells to display typical features of M cells, such as transcytosis activity, the disorganization of microvilli, and the expression of M cell markers. This transcytosis activity of MIE cells was not induced by T cells isolated from PPL costimulated with the same MAbs and was reduced by the depletion of the T cell population from PPL. A mixture of T cells treated with MAbs and B cells both from PPL led MIE cells to differentiate into M cells. We report here that MIE cells have the potential ability to differentiate into M cells and that this differentiation required activated T cells and B cells. |
| File Format | HTM / HTML |
| ISSN | 01931857 |
| Issue Number | 2 |
| Volume Number | 295 |
| e-ISSN | 15221547 |
| Journal | AJP: Gastrointestinal and Liver Physiology |
| Language | English |
| Publisher | American Physiological Society |
| Publisher Date | 2008-08-01 |
| Publisher Place | United States |
| Access Restriction | Subscribed |
| Subject Keyword | Discipline Physiology Discipline Gastroenterology Cell Differentiation Physiology Cell Lineage Intestinal Mucosa Cytology Animals Cell Line Coculture Techniques Ultrastructure Male Mice Mice, Inbred Balb C Microscopy, Phase-contrast Peyer's Patches Specific Pathogen-free Organisms Journal Article Research Support, Non-u.s. Gov't |
| Content Type | Text |
| Resource Type | Article |
| Subject | Hepatology Physiology Physiology (medical) Gastroenterology |
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