Volume 48, Issue 5 pp. 705-720
ORIGINAL ARTICLE CLINICAL PERIODONTOLOGY

Gene expression profiles of oral soft tissue-derived fibroblast from healing wounds: correlation with clinical outcome, autophagy activation and fibrotic markers expression

Mariana Andrea Rojas

Corresponding Author

Mariana Andrea Rojas

Department of Oral and Maxillofacial Sciences, Section of Periodontics, Sapienza University of Rome, Rome, Italy

Correspondence

Mariana Andrea Rojas, Section of Periodontics, Department of Oral and Maxillofacial Sciences, Sapienza University of Rome, 6 Caserta Street, Rome 00161, Italy.

Email: [email protected]

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Simona Ceccarelli

Simona Ceccarelli

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy

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Giulia Gerini

Giulia Gerini

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy

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Enrica Vescarelli

Enrica Vescarelli

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy

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Lorenzo Marini

Lorenzo Marini

Department of Oral and Maxillofacial Sciences, Section of Periodontics, Sapienza University of Rome, Rome, Italy

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Cinzia Marchese

Cinzia Marchese

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy

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Andrea Pilloni

Andrea Pilloni

Department of Oral and Maxillofacial Sciences, Section of Periodontics, Sapienza University of Rome, Rome, Italy

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First published: 01 February 2021
Citations: 10

Rojas and Ceccarelli are contributed equally.

Funding information

The study was self-funded by the authors and their institution.

Abstract

Aim

Our aim was to evaluate gene expression profiling of fibroblasts from human alveolar mucosa (M), buccal attached gingiva (G) and palatal (P) tissues during early wound healing, correlating it with clinical response.

Materials and Methods

M, G and P biopsies were harvested from six patients at baseline and 24 hr after surgery. Clinical response was evaluated through Early wound Healing Score (EHS). Fibrotic markers expression and autophagy were assessed on fibroblasts isolated from those tissues by Western blot and qRT-PCR. Fibroblasts from two patients were subjected to RT2 profiler array, followed by network analysis of the differentially expressed genes. The expression of key genes was validated with qRT-PCR on all patients.

Results

At 24 hr after surgery, EHS was higher in P and G than in M. In line with our clinical results, no autophagy and myofibroblast differentiation were observed in G and P. We observed significant variations in mRNA expression of key genes: RAC1, SERPINE1 and TIMP1, involved in scar formation; CDH1, ITGA4 and ITGB5, contributing to myofibroblast differentiation; and IL6 and CXCL1, involved in inflammation.

Conclusions

We identified some genes involved in periodontal soft tissue clinical outcome, providing novel insights into the molecular mechanisms of oral repair (ClinicalTrial.gov-NCT04202822).

CONFLICT OF INTEREST

The authors declare that they have no conflict of interests.

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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