Premium
The effects of 2‐hydroxyethyl methacrylate on matrix metalloproteinases 2 and 9 in human pulp cells and odontoblast‐like cells in vitro
Author(s) -
Sun S.,
Wang G.l.,
Huang Y.,
Diwu H.l.,
Luo Y.c.,
Su J.,
Xiao Y.h.
Publication year - 2018
Publication title -
international endodontic journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.988
H-Index - 119
eISSN - 1365-2591
pISSN - 0143-2885
DOI - 10.1111/iej.12812
Subject(s) - viability assay , odontoblast , dentin sialophosphoprotein , pulp (tooth) , chemistry , zymography , methacrylate , alkaline phosphatase , matrix metalloproteinase , bone sialoprotein , cell counting , cell , pulp capping , microbiology and biotechnology , biochemistry , osteocalcin , dentistry , biology , medicine , enzyme , cell cycle , monomer , organic chemistry , polymer
Aim To assess the effects of 2‐hydroxyethyl methacrylate ( HEMA ) on proliferation and migration of human pulp cells, as well as on matrix metalloproteinase ( MMP ‐2 and MMP ‐9) expression in human odontoblast‐like cells, contributing to the goal of determining the relationship between resin materials and MMP activity in pulp–dentine complexes. Methodology Dental pulp cell cultures were established from pulp tissue of human teeth extracted for orthodontic purposes. Pulp cell differentiation was characterized in the presence of dentine sialophosphoprotein, bone sialoprotein and alkaline phosphatase by reverse transcription polymerase chain reaction. MMP activity was assessed by gelatine zymography with media containing HEMA . Cell viability was evaluated using methyl thiazolyl tetrazolium assay for 24–72 h. Cell migration was tested using Transwell migration assay. Western blotting was used to visualize MMP expression with the nontoxic HEMA concentrations (0–400 μg mL −1 ) for 48 h. Results Pulp cell proliferation decreased with HEMA exposure in a time‐ and concentration‐dependent manner. HEMA concentrations ≤400 μg mL −1 did not induce changes in cell viability at 48 h ( P < 0.05). Pulp cells were induced to differentiate into odontoblast‐like cells in media containing 5 mg mL −1 ascorbic acid and 10 mmol L −1 β‐sodium glycerophosphate for 3–4 weeks. After incubation with HEMA , dose‐dependent inhibition was observed; HEMA had a strong inhibitory effect on MMP activity. Compared with the control group, cell migration and MMP expression were inhibited significantly with increasing HEMA concentration at noncytotoxic doses ( P < 0.05). Conclusions Cell viability was not affected at HEMA concentrations ≤400 μg mL −1 . Within this range, HEMA inhibited MMP ‐2 and MMP ‐9 expression and activity, which may protect against type I collagen degradation effectively during dentine adhesive procedures.