Related Experiment Video
Updated: Aug 4, 2026

16:01
Investigating Mast Cell Secretory Granules; from Biosynthesis to Exocytosis
Published on: January 26, 2015
Summary
Antisera to immunoglobulin G (IgG) subclasses triggered histamine release from rat mast cells, similar to anti-immunoglobulin E (IgE). This indicates IgG subclasses can activate mast cells, contributing to allergic responses.
Area of Science:
- Immunology
- Allergy Research
- Cellular Signaling
Background:
- Mast cells are key players in allergic reactions, primarily activated by immunoglobulin E (IgE).
- The role of immunoglobulin G (IgG) subclasses in mast cell activation is less understood.
- Investigating IgG subclass involvement can reveal new mechanisms in allergic and immune responses.
Purpose of the Study:
- To determine if antisera to rat IgG subclasses can induce histamine release from mast cells.
- To compare the histamine-releasing capacity of IgG subclass-specific antibodies with IgE.
- To elucidate the role of IgE in modulating IgG-induced mast cell activation.
Main Methods:
- Peritoneal mast cells were isolated from Lister hooded and Wistar rats.
- Cells were challenged with antisera specific to rat IgG subclasses (IgG1, IgG2a, IgG2b, IgG2c) and IgE.
- Histamine release was measured to quantify mast cell degranulation.
- Passive and active sensitization protocols were employed.
- Inhibition assays using IgE myeloma serum and purified IgE were performed.
Main Results:
- Antisera to IgG1 and IgG2a induced significant histamine release from Lister hooded rat mast cells, comparable to anti-IgE.
- Wistar rats, typically unresponsive, showed a small but significant histamine release upon active sensitization with IgG subclass-specific antisera.
- IgE myeloma serum and purified IgE inhibited histamine release induced by anti-IgE and, to varying degrees, by anti-IgG subclass antisera.
- Heating IgE abolished its inhibitory effect, suggesting IgE's role in IgG-mediated histamine release.
Conclusions:
- Rat IgG subclasses, particularly IgG1 and IgG2a, can directly activate mast cells to release histamine.
- IgE plays a complex role in modulating mast cell responses to IgG subclasses.
- These findings suggest potential alternative pathways for mast cell activation in allergic conditions beyond IgE.
Related Concept Videos
G-protein Coupled Receptors
G-protein coupled receptors are ligand binding receptors that indirectly affect changes in the cell. The actual receptor is a single polypeptide that transverses the cell membrane seven times creating intracellular and extracellular loops. The extracellular loops create a ligand specific pocket which binds to neurotransmitters or hormones. The intracellular loops holds onto the G-protein.
Inflammation
Overview
G Protein-coupled Receptors
G Protein-Coupled Receptors or GPCRs are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to sensory stimuli such as light, odors, hormones, cytokines, or neurotransmitters.
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
GPCRs Regulate Adenylyl Cylase Activity
Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of cells.
Two...
Two...
Transducer Mechanism: G Protein–Coupled Receptors
G Protein–Coupled Receptors (GPCRs) are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to various stimuli. GPCRs regulate critical physiological pathways and are excellent drug targets for treating diseases such as diabetes, cancer, obesity, depression, or Alzheimer's. Nearly 35% of approved drugs implement their therapeutic effects by selectively interacting with specific GPCRs.
GPCRs are also called heptahelical, 7TM, or...
GPCRs are also called heptahelical, 7TM, or...
Cholinergic Receptors: Muscarinic
The pharmacological actions of acetylcholine are elicited via its binding to two families of cholinergic receptors or cholinoceptors, namely, muscarinic and nicotinic receptors. Muscarinic receptors are G protein-coupled receptors and have five subtypes, M1–M5. All mAChR subtypes are activated by acetylcholine and blocked by the antagonist, atropine.
The subtypes M1, M3, and M5 couple with the Gq subunit and activate the phospholipase C (PLC) activity, mobilizing intracellular Ca2+. Activation...
The subtypes M1, M3, and M5 couple with the Gq subunit and activate the phospholipase C (PLC) activity, mobilizing intracellular Ca2+. Activation...

