Expression of HMGB1 and HMGN2 in gingival tissues, GCF and PICF of periodontitis patients and peri-implantitis

High mobility group chromosomal protein B1 (HMGB1) and N2 (HMGN2), two members of High mobility group (HMG) family, play important role in inflammation. The purposes of this study were to investigate the expression of HMGB1 and HMGN2 in periodontistis. The expression of HMGB1 and HMGN2 mRNA in gingival tissues and gingival crevicular fluid (GCF) in chronic periodontitis (CP), generalized aggressive periodontitis (G-AgP) patients and healthy subjects was detected by real-time PCR. The protein level of HMGB1 and HMGN2 in peri-implant crevicular fluid (PICF), peri-implant crevicular fluid of peri-implantitis (PI-PICF) and normal patients was determined by Western blotting. Furthermore, IL-1â, IL-6, IL-8, TNF-á and HMGB1 levels in GCF, PI-PICF and healthy-PICF samples from different groups were determined by ELISA. HMGN2 expression was increased in inflamed gingival tissues and GCF from CP and G-ApG groups compared to control group. HMGB1 expression was the highest in the gingival tissues and GCF from CP patients and was accompanied by increased concentrations of IL-1â, IL-6, IL-8 proinflammaory cytokines. To our knowledge, this is the first study reporting that the expression of HMGB1 and HMGN2 was increased in the gingival tissues and GCF in CP and G-AgP and the PICF in PICF. Our data suggest that HMGB1 may be a potential target for the therapy of periodontitis and PI.

Properties of oligonucleosomes from active genes of rat liver.

Active chromatin fraction from rat liver nuclei has been isolated under the lower ionic strength conditions, to prevent salt induced rearrangement and exchange of linker histone H1. Salt induced higher order folding in these oligonucleosomes was determined by sedimentation, viscosity, aggregation and circular dichroism studies. Sedimentation studies indicate that upon raising the ionic strength from 25 mM to 65 mM (mainly NaCl), active oligonucleosomes show intrafragmental interaction and formation of soluble oligomers. These oligomers disaggregate into unfolded monomers at 90 mM ionic strength. In contrast, oligonucleosomes from inactive genes show gradual increase in intrafragmental higher order folding without any interfragmental interaction on raising salt concentration. A much higher decrease in viscosity of active oligonucleosomes in comparison to bulk oligonucleosomes also support the above conclusion. However, on raising salt concentration above 100 mM NaCl, both the chromatin fractions are capable of forming insoluble aggregates. Decrease in the molar ellipticities of bulk oligonucleosomes at 273 and 282 nm is observed on raising ionic strength from 25 mM to 65 mM. A different pattern of this decrease is observed in case of active oligonucleosomes, indicating adaptation of a different type of salt induced secondary structure of DNA in these oligonucleosomes. Melting profile of DNA from active and bulk chromatin suggests that the base composition of both the chromatin fractions is same.