Related Experiment Video
Updated: Jul 10, 2026

Isolation, Characterization and Functional Examination of the Gingival Immune Cell Network
Published on: February 16, 2016
Defective polymorphonuclear leukocyte formyl peptide receptor(s) in juvenile periodontitis
1Rosalind Russell Arthritis Research Laboratory, Department of Medicine, University of California, San Francisco 94143.
Abstract:
Juvenile periodontitis (JP) is a disease characterized by severe gingival infections. PMN from some JP patients exhibit abnormal chemotactic responsiveness when challenged with the synthetic formyl peptide, FMLP. While investigating PMN function in JP, we found a patient in whom abnormal PMN chemotactic responses to FMLP were associated with a defective population of PMN formyl peptide receptor(s) (FPR). JP PMN failed to respond chemotactically when challenged with FMLP, but exhibited normal chemotactic responses upon exposure to purified human C5a. Furthermore, JP PMN were capable of degranulating and generating superoxide anion radicals as well as normal PMN upon exposure to FMLP. Binding studies demonstrated that JP PMN had a diminution in the number of high-affinity FPR. Studies in which FPR was radiolabeled by chemical cross-linking demonstrated that JP PMN FPR exhibited the same molecular weight and N-linked glycosylation as normal PMN FPR. JP PMN FPR, however, was more resistant to papain cleavage than normal PMN FPR. Autoradiograms obtained from 2D-PAGE of normal and JP PMN FPR demonstrated decreased amounts of FPR isoforms in JP PMN.
Insights
Juvenile periodontitis (JP) involves abnormal neutrophil (PMN) responses to formyl peptide (FMLP). This study found JP patients have fewer high-affinity formyl peptide receptors (FPR), impacting chemotaxis.
Area of Science:
- Immunology
- Oral Biology
- Cell Biology
Background:
- Juvenile periodontitis (JP) is a severe gingival infection.
- Neutrophils (PMN) from some JP patients show impaired chemotaxis to formyl peptide (FMLP).
Purpose of the Study:
- Investigate PMN function in JP.
- Identify the cause of abnormal chemotactic responses to FMLP in JP patients.
Main Methods:
- Chemotaxis assays using FMLP and C5a.
- PMN degranulation and superoxide generation tests.
- FPR binding studies, radiolabeling, and 2D-PAGE.
Main Results:
- JP PMN failed to respond to FMLP but responded normally to C5a.
- JP PMN showed normal degranulation and superoxide generation with FMLP.
- JP PMN had diminished high-affinity FPR, with altered papain cleavage resistance and decreased isoforms.
Conclusions:
- Defective formyl peptide receptor (FPR) population contributes to abnormal PMN chemotaxis in JP.
- JP PMN exhibit functional defects in FPR, despite normal molecular weight and glycosylation.
Related Concept Videos
Differentiation of Common Myeloid Progenitor Cells
Streptococcal Pharyngitis

