Abstract
Mechanical stress induces a variety of biochemical and morphological reactions in
bone cell biology. This study aimed to investigate appropriate pressures of osteogenesis
on the biological responses of three-dimensional cultured human mandibular fracture
hematoma-derived cells by compressive loading. A total of six patients with mandibular
fractures who underwent open reduction internal fixation were included in the study.
During the operation, fracture hematomas that formed fibrin clots were manually removed
before irrigation. First, pressures were applied to human mandibular fracture hematoma-derived
cell-seeded collagen sponges. The collagen sponges were subjected to mechanical compression
using the loading equipment applied at non-compression, 0.5, or 1 mm. Compressive
loading was applied to the samples prior to compression at 0, 6, 12, or 24h. Collagen
sponge samples were collected for quantification of mRNA using several parameters
including: alkaline phosphatase(ALP), osteopontin (OPN), osterix (OSX), runt-related
gene 2 (Runx2), protein level and immunocytochemistry (anti-sclerostin). Among these
parameters, 0.5 mm compression group compared to the control group and the 1.0 mm
compression group upregulated the mRNA expression of OPN and OSX after 24h. Additionally,
a significantly higher OSX gene expression was observed in both the 0.5 mm and 1.0
mm groups after 6, 12, and 24 h of compression compared to the control group (p<0.05).
However, no significant differences were observed regarding the ALP and RUNX2 expression.
These results indicated an increased stimulation of osteogenesis of the mandibular
fracture line gap in the 0.5 mm compressed group compared to the control group and
the 1.0 mm compression group.
Keywords
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Article Info
Publication History
Accepted:
June 2,
2022
Received in revised form:
May 31,
2022
Received:
December 20,
2021
Publication stage
In Press Accepted ManuscriptIdentification
Copyright
© 2022 The British Association of Oral and Maxillofacial Surgeons. Published by Elsevier Ltd. All rights reserved.