The latest study from the Jill Roberts Institute, "The neuropeptide neuromedin U stimulates innate lymphoid cells and type 2 inflammation," was published on September 6 in Nature. To read more, click here.     Dr. Gregory Sonnenberg wins inaugural award from the Society for Mucosal Immunology. To read more, click here.  The Kenneth Rainin Foundation awarded Dr. Iliyan Iliev and colleagues from Mount Sinai a $250,000 Synergy Award to examine the composition of the fungal community in babies born to mothers with inflammatory bowel disease. To read more, click here. Dr. Randy Longman received the Irma T. Hirschl Career Scientist Award and the New York Crohn’s Foundation Award.    

The Jill Roberts Institute for Research in Inflammatory Bowel Disease

You are here

Anatomical localization of commensal bacteria in immune cell homeostasis and disease.

TitleAnatomical localization of commensal bacteria in immune cell homeostasis and disease.
Publication TypeJournal Article
Year of Publication2014
AuthorsFung, TC, Artis, D, Sonnenberg, GF
JournalImmunol Rev
Volume260
Issue1
Pagination35-49
Date Published2014 Jul
ISSN1600-065X
KeywordsAnimals, Disease Susceptibility, Gastrointestinal Tract, Homeostasis, Humans, Immunity, Mucosal, Lymphoid Tissue, Microbiota, Mucous Membrane
Abstract

<p>The mammalian gastrointestinal (GI) tract is colonized by trillions of beneficial commensal bacteria that are essential for promoting normal intestinal physiology. While the majority of commensal bacteria are found in the intestinal lumen, many species have also adapted to colonize different anatomical locations in the intestine, including the surface of intestinal epithelial cells (IECs) and the interior of gut-associated lymphoid tissues. These distinct tissue localization patterns permit unique interactions with the mammalian immune system and collectively influence intestinal immune cell homeostasis. Conversely, dysregulated localization of commensal bacteria can lead to inappropriate activation of the immune system and is associated with numerous chronic infectious, inflammatory, and metabolic diseases. Therefore, regulatory mechanisms that control proper anatomical containment of commensal bacteria are essential to maintain tissue homeostasis and limit pathology. In this review, we propose that commensal bacteria associated with the mammalian GI tract can be anatomically defined as (i) luminal, (ii) epithelial-associated, or (iii) lymphoid tissue-resident, and we discuss the role and regulation of these microbial populations in health and disease.</p>

DOI10.1111/imr.12186
Alternate JournalImmunol. Rev.
PubMed ID24942680
PubMed Central IDPMC4216679
Grant ListDP5 OD012116 / OD / NIH HHS / United States