Related Experiment Video
Updated: May 13, 2026

Real-Time Measurement of the Mitochondrial Bioenergetic Profile of Neutrophils
Published on: June 2, 2023
Neutrophil F-actin dynamics in Familial Mediterranean Fever: the unequal effect of colchicine on activated
Tigran K Davtyan1, Samvel A Avetisyan, Gagik S Hakobyan
1Laboratory of Immunology and Virology, "Armenicum" Research Centre, CJSC Armenicum, 37 Nalbandyan str., Yerevan 0001, Republic of Armenia. tigdav@excite.com
Abstract:
In the innate immune system, cellular adaptation regulates neutrophil activation and chemotaxis, which have a pivotal role in Familial Mediterranean Fever (FMF) pathogenesis. We investigated neutrophil F-actin, phagocytosis and macropinocytosis dynamics during neutrophil chemoattractant-dependent activation in FMF patients carrying mutations in the MEFV locus. We found that while a non-stimulated neutrophil shows an increased overall F-actin content in patients with FMF, the activation-dependent F-actin dynamics in the presence of chemoattractant peptide is significantly reduced. Neither overall F-actin content nor F-actin dynamics was changed in FMF patient's neutrophils in the presence of double doses of chemoattractant, while in healthy donors it occurred with significant reduction of F-actin content and dynamics. The neutrophil shows increased phagocytosis and macropinocytosis dynamics for a relatively short period, which may contribute to the decreasing of plasticity of the cellular cytoskeleton during FMF. Colchicine causes reduction of overall F-actin content and shows a distinctively unequal effect on chemoattractant-activated neutrophil F-actin dynamics in FMF patients compared with healthy donors. These data suggested that mutations in MEFV cause the dissolution of cellular adaptation to chemoattractant stimuli due to alterations in neutrophil F-actin and phagocytosis dynamics, which could serve as a major target for FMF treatment.
Insights
Familial Mediterranean Fever (FMF) neutrophils show impaired F-actin dynamics and cellular adaptation to chemoattractant stimuli. This dysfunction in neutrophil F-actin and phagocytosis may be a key therapeutic target for FMF.
Area of Science:
- Immunology
- Cell Biology
- Genetics
Background:
- Familial Mediterranean Fever (FMF) pathogenesis involves neutrophil activation and chemotaxis.
- MEFV gene mutations are linked to FMF and may affect neutrophil function.
Purpose of the Study:
- Investigate neutrophil F-actin, phagocytosis, and macropinocytosis dynamics in FMF patients.
- Understand the impact of MEFV mutations on neutrophil response to chemoattractants.
- Evaluate the effect of colchicine on neutrophil dynamics in FMF.
Main Methods:
- Analysis of neutrophil F-actin content and dynamics in FMF patients and healthy donors.
- Assessment of phagocytosis and macropinocytosis in neutrophils.
- Examination of neutrophil response to varying chemoattractant concentrations.
- Evaluation of colchicine's effect on neutrophil F-actin dynamics.
Main Results:
- FMF neutrophils exhibit increased basal F-actin but reduced activation-dependent F-actin dynamics.
- FMF neutrophils show altered responses to chemoattractant stimuli compared to healthy controls.
- Phagocytosis and macropinocytosis dynamics are transiently increased in FMF neutrophils.
- Colchicine differentially affects neutrophil F-actin dynamics in FMF patients versus healthy donors.
Conclusions:
- MEFV mutations disrupt neutrophil cellular adaptation to chemoattractant stimuli.
- Altered neutrophil F-actin and phagocytosis dynamics are central to FMF pathogenesis.
- These neutrophil dysfunctions represent potential therapeutic targets for FMF treatment.
Related Concept Videos
Actin Filament Depolymerization
In F-actin, the ADF/cofilin proteins...
Drugs that Destabilize Microtubules

