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1.
J Cell Biochem ; 118(7): 1653-1658, 2017 07.
Article in English | MEDLINE | ID: mdl-28195408

ABSTRACT

Stem cells transplantation is a promising therapy strategy for accelerating periodontal regeneration and reconstruction. Genetic modification could induce stem cells directional differentiation to facilitate recovery of physiological functions. In this study, we investigated the role and mechanism of miR-22 on human periodontal ligament stem cells (PDLSCs). First, a cellular model of osteogenic differentiation was first established by osteogenic inductive cocktail. Real-time PCR determined that expression of miR-22 was significantly increased during PDLSCs osteogenic differentiation. Alizirin red staining showed that overexpression of miR-22 in PDLSCs induced better mineralized nodule formation. Real-time PCR and Western blot further confirmed up-regulation of osteogenic genes Runx2 and OPN in miR-22-overexpressing PDLSCs. Conversely, inhibition of miR-22 delayed the process of PDLSCs osteogenic differentiation. Furthermore, Histone deacetylase 6 (HDAC6) was identified as a target gene of miR-22. Overexpression of miR-22 not only reduced the luciferase activity of the reporter containing the 3' untranslated region of HDAC6 mRNA, but also suppressed the endogenous protein expression of HDAC6. Rescue experiment showed that the promotion role of miR-22 in osteogenic differentiation could be relieved by overexpression of HDAC6. Meanwhile, overexpression of HDAC6 alone could also delay the osteogenic differentiation process. The results demonstrated that miR-22 promoted PDLSCs osteogenic differentiation by inhibiting HDAC6 expression, suggesting that miR-22 might be developed as a target of genetic modified stem cells therapy for periodontal diseases. J. Cell. Biochem. 118: 1653-1658, 2017. © 2017 Wiley Periodicals, Inc.


Subject(s)
Histone Deacetylase 6/metabolism , MicroRNAs/metabolism , Osteogenesis/physiology , Periodontal Ligament/cytology , Stem Cells/cytology , Stem Cells/metabolism , Adolescent , Blotting, Western , Cell Differentiation/genetics , Cell Differentiation/physiology , Child , Computational Biology , Histone Deacetylase 6/genetics , Humans , MicroRNAs/genetics , Osteogenesis/genetics , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction
2.
Zhonghua Kou Qiang Yi Xue Za Zhi ; 46(8): 458-62, 2011 Aug.
Article in Chinese | MEDLINE | ID: mdl-22169740

ABSTRACT

OBJECTIVE: To summarize the experiences in the treatment of complicated orbital fractures. METHODS: A total of 89 patients with complicated orbital fractures treated in Department of Oral and Maxillofacial Surgery, China Medical University from January 2005 to January 2010 were retrospectively reviewed. The classification of these cases included naso-orbital-ethmoid fracture, frontal orbital fracture and orbitozygomatic fracture. All patients were followed up for 6 - 36 months. RESULTS: The orbital frame was repaired or reconstructed in these patients. The function of lacrimal pathways was improved. All the patients and the physicians were satisfied with the surgical effects. However, recurrence of deformity after endophthalmas correction was found in several cases. CONCLUSIONS: The experiences, comprehensive management of complicated orbital fractures by team approaches, concluded from this study could be expanded. There are still challenges in the treatment of complicated orbital fractures, such as severe endophthalmas deformity, recurrence of endophthalmas deformity and malunion of complicated orbital fracture.


Subject(s)
Ethmoid Bone/injuries , Nasal Bone/injuries , Orbital Fractures/surgery , Plastic Surgery Procedures , Skull Fractures/surgery , Zygomatic Fractures/surgery , Adolescent , Adult , Aged , Enophthalmos/etiology , Enophthalmos/surgery , Ethmoid Bone/surgery , Female , Follow-Up Studies , Humans , Male , Middle Aged , Nasal Bone/surgery , Orbital Fractures/complications , Retrospective Studies , Skull Fractures/complications , Young Adult , Zygomatic Fractures/complications
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