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Related Experiment Video

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Three-dimensional Co-culture Model for Tumor-stromal Interaction
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Histamine stimulates human lung fibroblast migration.

Tadashi Kohyama1, Yasuhiro Yamauchi, Hajime Takizawa

  • 1Department of Respiratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan. koyama-tky@umin.ac.jp

Molecular and Cellular Biochemistry
|October 24, 2009
PubMed
Summary

Histamine stimulates human lung fibroblast migration, potentially impacting wound healing and lung fibrosis. This effect is mediated by the H4 receptor, as shown by inhibition with a specific antagonist.

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Area of Science:

  • Immunology and Cell Biology
  • Pulmonary Medicine

Background:

  • Histamine is a key mediator in allergic inflammation, released by mast cells and basophils.
  • Fibroblast migration is crucial for tissue repair and can contribute to fibrotic diseases.

Purpose of the Study:

  • To investigate the effect of histamine on the in vitro migration of human fetal lung fibroblasts (HFL-1).
  • To determine the role of histamine and its receptor in fibroblast chemotaxis towards human plasma fibronectin (HFn).

Main Methods:

  • Utilized the blind-well chamber technique to assess HFL-1 cell migration.
  • Tested histamine alone and in combination with HFn, a known chemoattractant.
  • Investigated the involvement of the H4 receptor using a specific antagonist (JNJ7777120) and pertussis toxin.

Main Results:

  • Histamine alone did not induce chemotaxis but significantly augmented HFn-induced HFL-1 migration (up to 290.6%).
  • The stimulatory effect exhibited a bell-shaped concentration-response curve and increased with time.
  • Inhibition by an H4 receptor antagonist and pertussis toxin confirmed H4 receptor mediation.

Conclusions:

  • Histamine stimulates human lung fibroblast migration, suggesting a role in regulating wound healing.
  • This histamine-induced fibroblast migration may contribute to the pathogenesis of lung fibrotic disorders.
  • The H4 receptor is implicated in mediating histamine's effects on lung fibroblasts.