Abstract | OBJECTIVES:
Hematoma quality (especially the fibrin matrix) plays an important role in the bone healing process. Here, we investigated the effect of interleukin-1 beta (IL-1β) on fibrin clot formation from platelet-poor plasma (PPP). METHODS: Five-milliliter of rat whole-blood samples were collected from the hepatic portal vein. All blood samples were firstly standardized via a thrombelastograph (TEG), blood cell count, and the measurement of fibrinogen concentration. PPP was prepared by collecting the top two-fifths of the plasma after centrifugation under 400 × g for 10 min at 20°C. The effects of IL-1β cytokines on artificial fibrin clot formation from PPP solutions were determined by scanning electronic microscopy (SEM), confocal microscopy (CM), turbidity, and clot lysis assays. RESULTS: The lag time for protofibril formation was markedly shortened in the IL-1β treatment groups (243.8 ± 76.85 in the 50 pg/mL of IL-1β and 97.5 ± 19.36 in the 500 pg/mL of IL-1β) compared to the control group without IL-1β (543.8 ± 205.8). Maximal turbidity was observed in the control group. IL-1β (500 pg/mL) treatment significantly decreased fiber diameters resulting in smaller pore sizes and increased density of the fibrin clot structure formed from PPP (P < 0.05). The clot lysis assay revealed that 500 pg/mL IL-1β induced a lower susceptibility to dissolution due to the formation of thinner and denser fibers. CONCLUSION: IL-1β can significantly influence PPP fibrin clot structure, which may affect the early bone healing process.
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Authors | Xin Wang, Yan Luo, Paul P Masci, Ross Crawford, Yin Xiao |
Journal | PloS one
(PLoS One)
Vol. 11
Issue 2
Pg. e0149775
( 2016)
ISSN: 1932-6203 [Electronic] United States |
PMID | 26909757
(Publication Type: Journal Article)
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Chemical References |
- IL1B protein, rat
- Interleukin-1beta
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Topics |
- Animals
- Blood Coagulation
- Fracture Healing
- Hematoma
(metabolism, pathology)
- Humans
- Interleukin-1beta
(metabolism)
- Rats
- Rats, Inbred F344
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