Objective: To investigate the effects of Transforming growth factor beta (TGFbeta) and recombinant human bone morphogenetic protein 2 (rhBMP2) on the proliferation and differentiation of human periodontal ligament fibroblasts (HPDLFs).
Methods: To observe the individual, simultaneous and sequential effects of TGFbeta and rhBMP2 on the proliferation, alkaline phosphatase (ALP) activity, osteocalcin (OC) synthesis and mineralized nodule formation of the cultured HPDLFs.
Results: TGFbeta significantly stimulated the proliferation of HPDLFs but had no effects on ALP activity, OC synthesis and mineralized nodule formation. RhBMP2 had no remarkable effect on the proliferation of HPDLFs, whereas significantly stimulated the ALP activity, OC synthesis and mineralized nodule formation. Co-treatment with TGFbeta and rhBMP2 led to intermediate effects on cell proliferation and differentiation. Pre-treatment with TGFbeta did not influence the subsequent rhBMP2 action on HPDLFs differentiation. Pre-treatment with rhBMP2 and subsequent with TGFbeta had a remarkable stimulation on HPDLFs differentiation.
Conclusion: RhBMP2 can stimulate the expression of osteoblastic phenotype of HPDLFs. TGFbeta significantly stimulated the rhBMP2 effects on the differentiation of HPDLFs. TGFbeta and BMP2 may act at different stages to promote HPDLFs differentiation towards the osteoblast phenotype.
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Dig Dis Sci
January 2025
Ningxia Medical University, Xing Qing Block, Shengli Street No.1160, Yin Chuan City, 750004, Ningxia Province, People's Republic of China.
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Department of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
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College of Life Science, Yangtze University, Jingzhou, 434025, China.
The complex interaction between circadian rhythms and physiological functions is essential for maintaining human health. At the heart of this interaction lies the PERIOD proteins (PERs), pivotal to the circadian clock, influencing the timing of physiological and behavioral processes and impacting oxidative stress, immune functionality, and tumorigenesis. PER1 orchestrates the cooperation of the enzyme GPX1, modulating mitochondrial dynamics in sync with daily rhythms and oxidative stress, thus regulating the mechanisms managing energy substrates.
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