The Dental Pulp Stem/Progenitor Cells-Mediated Inflammatory-Regenerative Axis

牙髓干细胞 祖细胞 细胞生物学 归巢(生物学) 干细胞 Wnt信号通路 再生(生物学) 牙髓(牙) 成牙本质细胞 再生医学 医学 生物 牙科 信号转导 生态学
作者
Karim M. Fawzy El‐Sayed,Randa Elsalawy,Nourhan Ibrahim,Mahenar Gadalla,Hadir Albargasy,Nehal Zahra,Sherouk Mokhtar,Nadine El Nahhas,Youssef El Kaliouby,Christof E. Dörfer
出处
期刊:Tissue Engineering Part B-reviews [Mary Ann Liebert, Inc.]
卷期号:25 (5): 445-460 被引量:43
标识
DOI:10.1089/ten.teb.2019.0106
摘要

Relying on their ease of isolation and remarkable tissue reparative/regenerative potential, dental pulp stem/progenitor cells (DPSCs) gained pronounced importance in the field of regenerative dentistry. Though inflammation is classically considered the reason for the damage of the dentin-pulpal complex, it continues to be an essential stage of any dentin-pulpal tissue repair or regeneration procedures. During their performance of a pulpal tissue repair or regeneration actions, DPSCs interact with their inflammatory microenvironment locally, possibly influencing their fate and the result of any DPSCs-mediated dentin-pulpal reparative/regenerative endeavor. Hence, this review aims at comprehensively elaborating on these complex interactions of DPSCs with their local pulpal inflammatory microenvironment, particularizing on the inflammatory aspects, affecting DPSCs' stemness, homing/migration, proliferation, differentiation as well as immunomodulation characteristics, and the potentially fundamental intracellular processes involved and their anticipated association with the noncanonical as well as canonical Wnt/β-Catenin intracellular signaling. Impact Statement This review particularizes on the current state of knowledge on the complex interrelation between dental pulp stem/progenitor cells and their pulpal inflammatory microenvironment; elaborates on inflammation aspects affecting their stemness, proliferation, migration/homing, differentiation and immunomodulation characteristics, and the fundamental intracellular processes involved and their anticipated association with the canonical and noncanonical Wnt pathways. All these aspects could significantly affect the dento-pulpal regenerative therapeutic approaches in vivo.

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