cells Review The Potential of FGF-2 in Craniofacial Bone Tissue Engineering: A Review Anita Novais 1,2, Eirini Chatzopoulou 1,2,3, Catherine Chaussain 1,2 and Caroline Gorin 1,2,* 1 Pathologies, Imagerie et Biothérapies Orofaciales, Université de Paris, URP2496, 1 rue Maurice Arnoux, 92120 Montrouge, France;
[email protected] (A.N.);
[email protected] (E.C.);
[email protected] (C.C.) 2 AP-HP Département d’Odontologie, Services d’odontologie, GH Pitié Salpêtrière, Henri Mondor, Paris Nord, Hôpital Rothschild, Paris, France 3 Département de Parodontologie, Université de Paris, UFR Odontologie-Garancière, 75006 Paris, France * Correspondence:
[email protected]; Tel./Fax: +33-(0)1-5807-6724 Abstract: Bone is a hard-vascularized tissue, which renews itself continuously to adapt to the mechanical and metabolic demands of the body. The craniofacial area is prone to trauma and pathologies that often result in large bone damage, these leading to both aesthetic and functional complications for patients. The “gold standard” for treating these large defects is autologous bone grafting, which has some drawbacks including the requirement for a second surgical site with quantity of bone limitations, pain and other surgical complications. Indeed, tissue engineering combining a biomaterial with the appropriate cells and molecules of interest would allow a new therapeutic approach to treat large bone defects while avoiding complications associated with a second surgical site. This review first outlines the current knowledge of bone remodeling and the different signaling pathways involved seeking to improve our understanding of the roles of each to be able to stimulate or inhibit them.