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Related Concept Videos

Structure and Function of Leukocytes01:21

Structure and Function of Leukocytes

An adult in good health typically has between 4,500 and 11,000 leukocytes, or white blood cells, per microliter of blood, which constitutes about 1% of the total blood volume. Unlike red blood cells, white blood cells contain a nucleus and other cellular organelles but do not have hemoglobin. Most white blood cells reside in connective tissues, particularly in lymphatic organs such as the lymph nodes, with only a small fraction present in circulating blood.
White blood cells protect the body...
Lymphoid Cells and Tissues01:18

Lymphoid Cells and Tissues

Lymphoid cells and tissues are integral to the immune system, which is crucial in maintaining our body's defense against harmful pathogens. They form the building blocks of lymphoid organs, which include the spleen, thymus, and lymph nodes.
Lymphoid cells consist of various types of immune system cells. These include B and T lymphocytes, which are responsible for producing antibodies and killing infected cells, respectively. Dendritic cells act as messengers between the innate and adaptive...
Secondary Lymphoid Organs01:15

Secondary Lymphoid Organs

Secondary organs, including lymph nodes, the spleen, and mucosa-associated lymphoid tissue (MALT), work harmoniously to protect us from disease and infection.
The spleen is a vital organ in the lymphatic system, nestled in the upper left side of the abdomen. It is composed of two primary regions: the red pulp and the white pulp, each having distinct functions. The red pulp performs a significant role in blood filtration. It efficiently purges the blood of old or damaged red blood cells and...
Cells of the Adaptive Immune Response01:23

Cells of the Adaptive Immune Response

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...
T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...

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Related Experiment Video

Updated: Jul 20, 2026

Isolation and Flow Cytometric Characterization of Murine Small Intestinal Lymphocytes
08:14

Isolation and Flow Cytometric Characterization of Murine Small Intestinal Lymphocytes

Published on: May 8, 2016

Normal human intestinal B lymphocytes. Increased activation compared with peripheral blood.

M G Peters1, H Secrist, K R Anders

  • 1Washington University School of Medicine, St. Louis, Missouri 63110.

The Journal of Clinical Investigation
|June 1, 1989
PubMed
Summary

Human intestinal immune cells, particularly B cells, are highly activated in vivo, secreting more antibodies, especially IgA, compared to peripheral blood mononuclear cells (PBMC). Large intestine B cells show greater activation and IgA secretion than small intestine B cells.

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Last Updated: Jul 20, 2026

Isolation and Flow Cytometric Characterization of Murine Small Intestinal Lymphocytes
08:14

Isolation and Flow Cytometric Characterization of Murine Small Intestinal Lymphocytes

Published on: May 8, 2016

Isolating Lymphocytes from the Mouse Small Intestinal Immune System
11:28

Isolating Lymphocytes from the Mouse Small Intestinal Immune System

Published on: February 28, 2018

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

Area of Science:

  • Immunology
  • Gastroenterology
  • Cell Biology

Background:

  • Intestinal mononuclear cells (IMCs) play a crucial role in mucosal immunity.
  • Understanding the activation state of IMCs is vital for comprehending gut defense mechanisms.

Purpose of the Study:

  • To investigate the in vivo activation status of normal human intestinal mononuclear cells.
  • To compare the activation and antibody secretion of intestinal B cells with peripheral blood mononuclear cells (PBMC).

Main Methods:

  • Isolation and analysis of mononuclear cells from the human intestine (small and large bowel) and peripheral blood.
  • Flow cytometry to assess cell surface activation antigens on B and T lymphocytes.
  • Quantification of immunoglobulin (Ig) secreting cells, with a focus on IgA.

Main Results:

  • Freshly isolated IMCs exhibited significantly higher expression of activation antigens on B and T lymphocytes compared to PBMC.
  • Intestinal mononuclear cells contained substantial numbers of spontaneous immunoglobulin-secreting cells, including CD5-positive B cells producing IgA.
  • Cells from the large intestine consistently showed higher numbers of IgA-secreting cells than those from the small intestine.

Conclusions:

  • Intestinal B cells are markedly activated in vivo, correlating with increased spontaneous antibody secretion.
  • B cells from the large intestine are more activated and secrete more IgA than those from the small intestine.
  • The heightened activation of the intestinal lamina propria lymphoid compartment suggests its critical role in mucosal defense.