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Related Concept Videos

Acute Inflammation II: Cellular Phase01:26

Acute Inflammation II: Cellular Phase

The cellular phase of acute inflammation is a tightly orchestrated sequence of events that recruits leukocytes, primarily neutrophils, to sites of tissue injury or infection. Following the initial vascular changes, this phase ensures effective immune cell migration, activation, and function at the affected site to eliminate pathogens and initiate tissue repair.Leukocyte Recruitment CascadeLeukocyte recruitment happens in four steps: margination, adhesion, transmigration, and chemotaxis. Reduced...
Selectins01:25

Selectins

Cell adhesion is  an essential aspect of multicellularity. While stable cell interactions usually occur between cells of the same type, transient cell interactions occur between cells of different tissue types, such as between neutrophils and endothelial cells. Selectins are one class of cell adhesion molecules (CAMs) that bind carbohydrate ligands to form transient cell adhesion. They are rod-like proteins with a long extracellular part of variable length ending with the lectin domain, which...
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...
Inflammation01:38

Inflammation

Overview
Acute Inflammation I: Inflammatory Response01:26

Acute Inflammation I: Inflammatory Response

Acute inflammation is a rapid, short-lived physiological response to tissue injury or infection, designed to eliminate harmful agents and initiate repair. This tightly regulated process typically lasts from minutes to several days and is triggered by factors such as microbial invasion, physical trauma, or chemical injury.Recognition and Mediator ReleaseThe inflammatory response begins when resident immune cells—such as mast cells, macrophages, and dendritic cells—detect damage-associated...
Acute Inflammation III: Local and Systemic Effects01:25

Acute Inflammation III: Local and Systemic Effects

Acute inflammation produces a coordinated set of local and systemic changes that limit injury, eliminate pathogens, and initiate repair. These responses arise within minutes of infection, trauma, or chemical insult and are driven by vascular alterations and leukocyte-derived mediators. When the stimulus resolves, the reaction typically abates within days.Local EffectsAt the site of injury, arteriolar vasodilation increases blood flow, resulting in redness and warmth. Simultaneously, increased...

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Related Experiment Video

Updated: Jun 22, 2026

A Microphysiological System to Study Leukocyte-Endothelial Cell Interaction during Inflammation
12:55

A Microphysiological System to Study Leukocyte-Endothelial Cell Interaction during Inflammation

Published on: December 9, 2021

Leukocyte-endothelial interactions in inflammation.

Harald F Langer1, Triantafyllos Chavakis

  • 1Experimental Immunology Branch, National Cancer Institute, NIH, Bethesda, MD, USA. langerh@mail.nih.gov

Journal of Cellular and Molecular Medicine
|June 23, 2009
PubMed
Summary

Leukocyte and platelet interactions with the endothelium are crucial for innate immunity during inflammation. This review details the molecular mechanisms governing these adhesive and transmigration processes.

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Screening Assays to Characterize Novel Endothelial Regulators Involved in the Inflammatory Response
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Screening Assays to Characterize Novel Endothelial Regulators Involved in the Inflammatory Response

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Related Experiment Videos

Last Updated: Jun 22, 2026

A Microphysiological System to Study Leukocyte-Endothelial Cell Interaction during Inflammation
12:55

A Microphysiological System to Study Leukocyte-Endothelial Cell Interaction during Inflammation

Published on: December 9, 2021

Assessing Leukocyte-endothelial Interactions Under Flow Conditions in an Ex Vivo Autoperfused Microflow Chamber Assay
09:01

Assessing Leukocyte-endothelial Interactions Under Flow Conditions in an Ex Vivo Autoperfused Microflow Chamber Assay

Published on: December 30, 2014

Screening Assays to Characterize Novel Endothelial Regulators Involved in the Inflammatory Response
12:50

Screening Assays to Characterize Novel Endothelial Regulators Involved in the Inflammatory Response

Published on: September 15, 2017

Area of Science:

  • Immunology
  • Cell Biology
  • Vascular Biology

Background:

  • Inflammation, infection, and vascular injury trigger leukocyte recruitment to endothelium.
  • Leukocyte-endothelial interactions are a multi-step cascade involving adhesion and transmigration.
  • Platelets contribute to inflammation by facilitating leukocyte-endothelial interactions.

Purpose of the Study:

  • To summarize key mechanisms and molecules in leukocyte-endothelial interactions.
  • To review the role of platelets in inflammatory pathologies.
  • To elucidate the molecular basis of leukocyte transmigration.

Main Methods:

  • Review of existing literature on leukocyte-endothelial and platelet interactions.
  • Analysis of molecular mediators like selectins and integrins.
  • Examination of transmigration routes (transcellular and paracellular).

Main Results:

  • Selectins mediate initial leukocyte rolling.
  • Chemokine-activated integrins cause firm leukocyte adhesion.
  • Leukocytes transmigrate via transcellular or paracellular routes.
  • Platelets enhance leukocyte-endothelial interactions.

Conclusions:

  • Leukocyte-endothelial and leukocyte-platelet interactions are vital for innate immunity in inflammation.
  • Understanding these interactions offers therapeutic targets for inflammatory diseases.
  • Platelet involvement highlights their multifaceted role in inflammatory responses.