4.6 Article

Proteome analysis of proteins related to aggressive periodontitis combined with neutrophil chemotaxis dysfunction

Journal

JOURNAL OF CLINICAL PERIODONTOLOGY
Volume 38, Issue 4, Pages 310-317

Publisher

WILEY
DOI: 10.1111/j.1600-051X.2010.01693.x

Keywords

Aggressive periodontitis; caldesmon; neutrophil chemotaxis dysfunction; two-dimensional fluorescence difference gel electrophoresis

Funding

  1. Japan Society for the Promotion of Science, Japan [21792122]
  2. Grants-in-Aid for Scientific Research [21792122, 21390557, 21310035] Funding Source: KAKEN

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P>Aim Some patients suffering from aggressive periodontitis (Ag-P) also display neutrophil chemotaxis dysfunction. In this study, we attempted to identify the proteins involved in Ag-P associated with neutrophil chemotaxis dysfunction using proteome analysis. Material and Methods A two-dimensional fluorescence difference gel electrophoresis system was used to detect differences in protein expression between neutrophils from four patients suffering from Ag-P combined with neutrophil chemotaxis dysfunction and those from four controls. Moreover, the mRNA levels of the proteins identified by the above method were examined in neutrophils from four types of subjects using the real-time polymerase chain reaction: twenty patients suffering from Ag-P with or without the dysfunction, 15 patients with chronic periodontitis, and 15 controls. Results Four proteins, lactoferrin, caldesmon, heat shock protein 70, and stac, displayed a higher protein expression level in the neutrophils from the patients suffering from Ag-P combined with the neutrophil dysfunction than in those from the control group. The caldesmon mRNA levels in the neutrophils from the patients suffering from Ag-P combined with the neutrophil dysfunction were high compared with those in the neutrophils from the patients suffering from the other two types of periodontitis and those from the control group. Conclusion Caldesmon may be a marker of Ag-P combined with neutrophil chemotaxis dysfunction.

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