4.6 Review

Autophagy Plays Multiple Roles in the Soft-Tissue Healing and Osseointegration in Dental Implant Surgery-A Narrative Review

Journal

MATERIALS
Volume 15, Issue 17, Pages -

Publisher

MDPI
DOI: 10.3390/ma15176041

Keywords

autophagy; osseointegration; dental implant; osteoimmunity; wound healing

Funding

  1. Carol Davila University of Medicine and Pharmacy Bucharest, Romania [CNFIS-FDI-2022-0253]
  2. Romanian Ministry of Education

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This review explores the role of autophagy in dental implant surgery. Autophagy plays important roles in regulating immune response, promoting cell survival, and regulating osteoblast function in macrophages, endothelial cells, and osteoblasts, respectively. It also plays a critical role in alveolar bone remodeling and fibroblast apoptosis. Autophagy seems to have a dual role in dental implant surgery and further research is needed to fully understand its positive features.
Dental endo-osseous implants have become a widely used treatment for replacing missing teeth. Dental implants are placed into a surgically created osteotomy in alveolar bone, the healing of the soft tissue lesion and the osseointegration of the implant being key elements to long-term success. Autophagy is considered the major intracellular degradation system, playing important roles in various cellular processes involved in dental implant integration. The aim of this review is an exploration of autophagy roles in the main cell types involved in the healing and remodeling of soft tissue lesions and implant osseointegration, post-implant surgery. We have focused on the autophagy pathway in macrophages, endothelial cells; osteoclasts, osteoblasts; fibroblasts, myofibroblasts and keratinocytes. In macrophages, autophagy modulates innate and adaptive immune responses playing a key role in osteo-immunity. Autophagy induction in endothelial cells promotes apoptosis resistance, cell survival, and protection against oxidative stress damage. The autophagic machinery is also involved in transporting stromal vesicles containing mineralization-related factors to the extracellular matrix and regulating osteoblasts' functions. Alveolar bone remodeling is achieved by immune cells differentiation into osteoclasts; autophagy plays an important and active role in this process. Autophagy downregulation in fibroblasts induces apoptosis, leading to better wound healing by improving excessive deposition of extracellular matrix and inhibiting fibrosis progression. Autophagy seems to be a dual actor on the scene of dental implant surgery, imposing further research in order to completely reveal its positive features which may be essential for clinical efficacy.

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