Vitamin D attenuates human gingival fibroblast inflammatory cytokine production following advanced glycation end product interaction with receptors for AGE
| Autor: | Martina Elenkova, David A. Tipton, Sidney H. Stein, Anastasios Karydis |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
Glycation End Products Advanced medicine.medical_specialty medicine.medical_treatment Interleukin-1beta Receptor for Advanced Glycation End Products Gingiva Inflammation Stimulation Serum Albumin Human vitamin D deficiency Cell Line 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Calcitriol Glycation Internal medicine medicine Vitamin D and neurology Diabetes Mellitus Humans Receptor Periodontitis Cholecalciferol Chemistry Interleukin-6 Interleukin-17 Interleukin-8 030206 dentistry Fibroblasts medicine.disease Stimulation Chemical body regions Endotoxins 030104 developmental biology Cytokine Endocrinology Depression Chemical embryonic structures Periodontics Advanced glycation end-product medicine.symptom Inflammation Mediators |
| Zdroj: | Journal of periodontal research. 54(2) |
| ISSN: | 1600-0765 |
| Popis: | Background and objectives Vitamin D [1,25(OH)2 D3 or 1,25D3] is critical in musculoskeletal health, inflammation, immune response, and glucose metabolism. Patients with vitamin D deficiency may be at higher risk of diabetes and periodontitis. Diabetic patients exhibit exacerbated inflammation and more periodontal destruction. Advanced glycation end products (AGEs), formed during diabetic hyperglycemia, activate inflammatory pathways in periodontitis. Human gingival fibroblasts (HGFs) express receptors for AGEs (RAGEs) and can contribute to inflammation. Objectives Determine whether glycated human serum albumin (G-HSA) augments HGF IL-6 and IL-8 production, and whether treatment with 1,25D3 attenuates cytokine production following stimulation with G-HSA + IL-1β and/or IL-17. Material and methods HGFs were incubated ±G-HSA or normal human serum albumin (HSA), ±IL-1β and/or IL-17, ±1,25D3. Cytokines were measured by ELISA. Neutralizing anti-RAGE was used to assess AGE-RAGE interaction. Endotoxin was measured using the ToxinSensor™ System. Data were expressed as mean ± standard deviation and analyzed using a one-way analysis of variance (ANOVA) and Scheffe's F procedure for post hoc comparisons. Results G-HSA or IL-1β, but not HSA, significantly stimulated IL-6 and IL-8 production. G-HSA or HSA when combined with IL-1β or IL-1β + IL-17 synergistically stimulated IL-6 and IL-8. Neutralizing anti-RAGE inhibited IL-6 and IL-8 produced by cells stimulated with IL-1β + G-HSA but not (+HSA). Synergism caused by HSA did not appear to be mediated by endotoxin since its levels in G-HSA and HSA were not sufficient to stimulate fibroblasts. Vitamin D inhibited IL-6 and IL-8 production stimulated by G-HSA or HSA + IL-1β or IL-1β + IL-17. Conclusions Results suggest that the "perioprotective" effects of vitamin D are related to its ability to regulate inflammatory cytokine production by HGFs following AGE-RAGE interaction. |
| Databáze: | OpenAIRE |
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