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Related Concept Videos

Renewal of Intestinal Stem Cells01:23

Renewal of Intestinal Stem Cells

The intestinal epithelial lining rapidly renews every 4 to 5 days. The renewal is facilitated by intestinal stem cells (ISCs) located at the base of the crypt– a gland located at the bottom of each villus. ISCs divide asymmetrically to form new stem cells and progenitor daughter cells. The daughter cells are called transit-amplifying (TA) cells which move upwards along the crypt and either differentiate into absorptive cells– the enterocytes or secretory cells– including the goblet,...
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The T and B lymphocytes of the adaptive immune system develop from common lymphoid progenitor cells in the bone marrow. These progenitors give rise to precursors that eventually develop into both T and B lymphocytes. As these precursors mature, they gain the ability to detect and respond to foreign antigens in the body, a process known as immunocompetence. Additionally, these precursors acquire self-tolerance, a process that ensures they do not react to self-antigens. This intricate system...
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Cell migration is a process by which the cells move from one location to another, playing an essential role in embryological development, repair and regeneration, immune response, and metastasis. Cells migrate in response to chemical or mechanical signals generated by specific organs or tissues. The overall mechanism includes three steps - polarization, protrusion, and release. Polarization involves the formation of a distinct cell front and rear, which determines the direction of movement.
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Cell migration, the process by which cells move from one location to another, is essential for the proper development and viability of organisms throughout their life. When cells are not able to migrate properly to their ordained locations, various disorders may occur. For example, disruption in cell migration causes chronic inflammatory diseases such as arthritis.

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Related Experiment Video

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Intravital Imaging of Intraepithelial Lymphocytes in Murine Small Intestine
08:00

Intravital Imaging of Intraepithelial Lymphocytes in Murine Small Intestine

Published on: June 24, 2019

Dynamic T cell migration program provides resident memory within intestinal epithelium.

David Masopust1, Daniel Choo, Vaiva Vezys

  • 1Department of Microbiology, Center for Immunology, University of Minnesota, Minneapolis, MN 55455, USA. masopust@umn.edu

The Journal of Experimental Medicine
|February 17, 2010
PubMed
Summary
This summary is machine-generated.

Activation in the spleen, not just local gut tissue, can prime T cells for intestinal homing. This explains how systemic immunizations induce gut immunity and highlights dynamic T cell migration patterns.

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Area of Science:

  • Immunology
  • Cellular Biology
  • Gastroenterology

Background:

  • Intestinal T cell homing was thought to depend solely on local activation within gastrointestinal lymphoid tissues.
  • This model conflicted with observations of intestinal T cell responses following non-gastrointestinal immunization routes.

Purpose of the Study:

  • To reconcile the discrepancy between local activation models and observed systemic induction of intestinal immunity.
  • To investigate the role of splenic activation in T cell homing to the intestinal mucosa.
  • To characterize the recirculation dynamics of memory T cells in the intestinal epithelium.

Main Methods:

  • Comparative analysis of T cell homing molecule expression after activation in different lymphoid tissues (gastrointestinal vs. spleen vs. skin-draining lymph nodes).
  • Tracking of memory T cell populations within the small intestine epithelium and other tissues.
  • Investigation of human T cell homing dynamics following subcutaneous yellow fever vaccination.

Main Results:

  • Splenic activation induces an intermediate level of intestinal homing potential in T cells.
  • Memory T cells in the small intestine epithelium do not consistently recirculate with those in other tissues.
  • T cell homing dynamics observed in the study are mirrored in human immune responses to yellow fever vaccination.

Conclusions:

  • Splenic activation contributes to the seeding of the intestine with T cells capable of homing to the intestinal mucosa.
  • The intestinal immune system is populated by memory T cell precursors shortly after systemic activation events.
  • T cell homing to the intestine is a dynamic process influenced by the site of initial immune activation.