Leptin in Dental Pulp and Periapical Tissues: A Narrative Review.
Jenifer Martin-GonzalezJuan Jose Segura-EgeaAntonio Pérez-PérezDaniel Cabanillas-BalseraVíctor Sánchez-MargaletPublished in: International journal of molecular sciences (2022)
Leptin is a non-glycosylated 16 kDa protein synthesized mainly in adipose cells. The main function of leptin is to regulate energy homeostasis and weight control in a central manner. There is increasing evidence that leptin also has systemic effects, acting as a link between innate and acquired immune responses. The expression of leptin and its receptor in human dental pulp and periradicular tissues have already been described, as well as several stimulatory effects of leptin protein expression in dental and periodontal tissues. The aim of this paper was to review and to compile the reported scientific literature on the role and effects of leptin in the dental pulp and periapical tissues. Twelve articles accomplished the inclusion criteria, and a comprehensive narrative review was carried out. Review of the available scientific literature concluded that leptin has the following effects on pulpal and periapical physiology: 1) Stimulates odontogenic differentiation of dental pulp stem cells (DPSCs), 2) Increases the expression of dentin sialophosphoprotein (DSPP) and dentin matrix protein-1 (DMP-1), odontoblastic proteins involved in odontoblastic differentiation and dentin mineralization, 3) Stimulates vascular endothelial growth factor (VEGF) expression in human dental pulp tissue and primary cultured cells of human dental pulp (hDPCs), 4) Stimulates angiogenesis in rat dental pulp cells, and 5) Induces the expression of interleucinas 6 and 8 in human periodontal ligament cells (hPDLCs). There is evidence which suggests that leptin is implicated in the dentin mineralization process and in pulpal and periapical inflammatory and reparative responses.
Keyphrases
- endothelial cells
- induced apoptosis
- vascular endothelial growth factor
- poor prognosis
- stem cells
- immune response
- cell cycle arrest
- binding protein
- oxidative stress
- systematic review
- induced pluripotent stem cells
- pluripotent stem cells
- endoplasmic reticulum stress
- adipose tissue
- body mass index
- signaling pathway
- metabolic syndrome
- cell death
- type diabetes
- dendritic cells
- insulin resistance
- inflammatory response
- skeletal muscle
- small molecule
- mesenchymal stem cells
- cell proliferation
- cone beam computed tomography
- weight loss
- drug induced