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Investigating Mast Cell Secretory Granules; from Biosynthesis to Exocytosis
Published on: January 26, 2015
Gastrin induces histamine release from human cutaneous mast cells
The Journal of Allergy and Clinical Immunology
|August 1, 1984
Summary
Gastrin (G17) and pentagastrin stimulate histamine release from skin mast cells. This gastrin-induced mast cell mediator release may play a role in allergic disorders.
Area of Science:
- Immunology
- Gastroenterology
- Dermatology
Background:
- Human gastrin I (G17) is a hormone involved in digestion.
- Cutaneous mast cells are key players in allergic reactions and inflammation.
- The interaction between gastrin and mast cells is not fully understood.
Purpose of the Study:
- To investigate the effect of gastrin and its analogs on histamine release from human skin mast cells.
- To determine if the carboxy-terminal region of gastrin is responsible for mast cell stimulation.
- To explore the in vivo relevance of gastrin's effect on mast cells.
Main Methods:
- In vitro studies using human cutaneous mast cells.
- Dose-response experiments with gastrin I (G17) and pentagastrin.
- In vivo intradermal administration in normal subjects and a patient with mastocytosis.
Main Results:
- Physiologic concentrations of G17 and pentagastrin induced dose-related histamine release from mast cells in vitro.
- The N-terminal fragment (G1-13) did not stimulate or block histamine release.
- Intradermal G17 and pentagastrin caused wheal-and-flare responses in vivo, particularly in mastocytosis.
Conclusions:
- Physiologic gastrin concentrations can stimulate mediator release from human cutaneous mast cells.
- The carboxy-terminal region of gastrin appears to mediate this mast cell response.
- Gastrin-induced mast cell activation may be relevant in allergic disorders and mast cell research.
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