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Related Concept Videos

Ischemic Stroke ll: Pathophysiology01:15

Ischemic Stroke ll: Pathophysiology

An ischemic stroke occurs when a cerebral blood vessel becomes obstructed, most often by a thrombus or embolus, interrupting the delivery of oxygen and glucose to brain tissue. Because neurons rely on continuous aerobic metabolism, energy failure begins within minutes of reduced perfusion. The region receiving the least blood flow becomes the infarct core, an area of irreversible cellular death. Surrounding this core lies the penumbra, a zone of hypoperfused but still viable tissue that is...
Transient Ischemic Attack l: Introduction01:26

Transient Ischemic Attack l: Introduction

A transient ischemic attack (TIA) is a brief episode of neurological dysfunction caused by a temporary, focal reduction in cerebral blood flow. Although symptoms resemble those of an ischemic stroke, the interruption in perfusion is short-lived and does not cause permanent infarction. TIAs are clinically important because they often serve as early warning events for future stroke.Mechanisms of Transient Cerebral IschemiaTransient cerebral ischemia may arise through several mechanisms. One...

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Updated: Jun 22, 2026

Isolation and Flow Cytometric Analysis of Immune Cells from the Ischemic Mouse Brain
12:14

Isolation and Flow Cytometric Analysis of Immune Cells from the Ischemic Mouse Brain

Published on: February 12, 2016

Transient decrease in circulating dendritic cell precursors after acute stroke: potential recruitment into the brain.

Atilla Yilmaz1, Tanja Fuchs, Barbara Dietel

  • 1Clinic of Internal Medicine I, Department of Cardiology, University Hospital Jena, Jena, Germany. A.Yilmaz@web.de

Clinical Science (London, England : 1979)
|June 11, 2009
PubMed
Summary
This summary is machine-generated.

Acute stroke significantly reduces circulating dendritic cell precursors (DCPs), which are recruited to the brain, potentially triggering immune responses. Numbers recover in the days following stroke.

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Area of Science:

  • Neuroimmunology
  • Cerebrovascular Diseases
  • Inflammation

Background:

  • Dendritic cells (DCs) are key immune mediators, but their role in stroke remains under-investigated.
  • Understanding DC dynamics in stroke is crucial for developing targeted therapies.

Purpose of the Study:

  • To investigate circulating myeloid DC precursors (mDCPs), plasmacytoid DCPs (pDCPs), and total DCPs in various stroke types.
  • To correlate DCP levels with stroke severity, infarct size, and inflammatory markers.
  • To examine DC infiltration in the infarcted brain.

Main Methods:

  • Flow cytometry analysis of circulating DCPs in healthy controls and patients with stroke (ACI-S, TIA, AIS, AHS).
  • Evaluation of NIHSS and CT-determined infarct size.
  • Post-mortem immunohistochemical analysis of brain tissue for DCs, T-cells, and HLA-DR.

Main Results:

  • Acute ischemic stroke (AIS) and acute hemorrhagic stroke (AHS) showed significantly reduced circulating mDCPs, pDCPs, and tDCPs.
  • Circulating DCP levels inversely correlated with NIHSS scores and hsCRP levels.
  • Larger infarct sizes were associated with lower DCP counts, with recovery observed in early follow-up.

Conclusions:

  • Acute stroke causes a significant decrease in circulating dendritic cell precursors.
  • Circulating DCPs are likely recruited to the infarcted brain, contributing to cerebral immune responses.
  • These findings highlight the involvement of DCs in stroke-related inflammation.