Literature DB >> 15580658

Cryptopatches and isolated lymphoid follicles: dynamic lymphoid tissues dispensable for the generation of intraepithelial lymphocytes.

Oliver Pabst1, Heike Herbrand, Tim Worbs, Michaela Friedrichsen, Sheng Yan, Matthias W Hoffmann, Heiner Körner, Günter Bernhardt, Reinhard Pabst, Reinhold Förster.   

Abstract

In comparison to secondary lymphoid organs, gut-associated lymphoid tissues such as isolated lymphoid follicles (ILF) and cryptopatches (CP) have been less intensively studied. To gain a better insight into processes regulating organization and function of these structures, which are believed to participate in immune responses and extrathymic T cell development, we characterized the lymphoid structures of the murine small intestine in more detail. The size and cellular composition of small intestinal lymphoid aggregations were analyzed in C57BL/6 and BALB/c wild-type and lymphotoxin (LT)-deficient mice, by flow cytometry, histology and automated multi-color immunofluorescence microscopy evaluating large coherent areas of the intestine. These evaluations demonstrate that aggregated lymphoid structures in the small intestine vary in size and cellular composition, with a majority of structures not matching the current definitions of CP or ILF. Accordingly, significant variations depending on species, age and mouse strain were observed. Furthermore, small bowel transplantation revealed a rapid exchange of B but not T cells between host and grafted tissue. Moreover, LT-deficient animals lack any intestinal lymphoid aggregations yet possess the complete panel of intraepithelial lymphocytes (IEL). In summary, our observations disclose intestinal lymphoid aggregations as dynamic structures with a great deal of inborn plasticity and demonstrate their dispensability for the generation of IEL.

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Year:  2005        PMID: 15580658     DOI: 10.1002/eji.200425432

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  57 in total

1.  Dendritic cells produce CXCL13 and participate in the development of murine small intestine lymphoid tissues.

Authors:  Keely G McDonald; Jacquelyn S McDonough; Brian K Dieckgraefe; Rodney D Newberry
Journal:  Am J Pathol       Date:  2010-03-19       Impact factor: 4.307

Review 2.  Lymphoid organogenesis in the intestine.

Authors:  Rebekah T Taylor; Ifor R Williams
Journal:  Immunol Res       Date:  2005       Impact factor: 2.829

3.  CCR9 is a homing receptor for plasmacytoid dendritic cells to the small intestine.

Authors:  Meike Wendland; Niklas Czeloth; Nicolas Mach; Bernard Malissen; Elisabeth Kremmer; Oliver Pabst; Reinhold Förster
Journal:  Proc Natl Acad Sci U S A       Date:  2007-04-02       Impact factor: 11.205

4.  Foxp3-expressing CD103+ regulatory T cells accumulate in dendritic cell aggregates of the colonic mucosa in murine transfer colitis.

Authors:  Frank Leithäuser; Tamara Meinhardt-Krajina; Kerstin Fink; Beate Wotschke; Peter Möller; Jörg Reimann
Journal:  Am J Pathol       Date:  2006-06       Impact factor: 4.307

Review 5.  Induction of intestinal lymphoid tissue formation by intrinsic and extrinsic signals.

Authors:  Daniela Finke
Journal:  Semin Immunopathol       Date:  2009-06-09       Impact factor: 9.623

Review 6.  Role of mucosal dendritic cells in inflammatory bowel disease.

Authors:  Jan Hendrik Niess
Journal:  World J Gastroenterol       Date:  2008-09-07       Impact factor: 5.742

Review 7.  Development of secondary lymphoid organs.

Authors:  Troy D Randall; Damian M Carragher; Javier Rangel-Moreno
Journal:  Annu Rev Immunol       Date:  2008       Impact factor: 28.527

Review 8.  The regulation of gut mucosal IgA B-cell responses: recent developments.

Authors:  N Y Lycke; M Bemark
Journal:  Mucosal Immunol       Date:  2017-07-26       Impact factor: 7.313

Review 9.  Re-thinking the functions of IgA(+) plasma cells.

Authors:  Jennifer L Gommerman; Olga L Rojas; Jörg H Fritz
Journal:  Gut Microbes       Date:  2014

10.  Intestinal CD103+, but not CX3CR1+, antigen sampling cells migrate in lymph and serve classical dendritic cell functions.

Authors:  Olga Schulz; Elin Jaensson; Emma K Persson; Xiaosun Liu; Tim Worbs; William W Agace; Oliver Pabst
Journal:  J Exp Med       Date:  2009-12-14       Impact factor: 14.307

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