Geometry of Artificial ECM: Sizes of Pores Controlling Phenotype Expression in BMP-Induced Osteogenesis and Chondrogenesis

This study aims to elucidate the feasible geometry of the scaffolds in bone and periodontal tissue engineering. Several biomaterials with different geometries are compared in terms of their patterns of ectopic BMP-induced chondrogenesis and osteogenesis. The materials include a honeycomb-shaped hydroxyapatite (HCHAP) with different tunnel sizes, a laser-perforated collagen membrane (LPM), and CPSA bioglass fibers. Implanted pellets were removed at 1-4 weeks and analyzed for bone and cartilage formation histologically and biochemically. Porous particles of hydroxyapatite (PPHAP), porous blocks of hydroxyapatite (PBHAP), and LPM did not induce detectable cartilage formation. In straight tunnel structures with various diameters in honeycomb-shaped hydroxyapatite (HCHAP), tunnels with smaller diameters (approximately 0.1 mm) induced cartilage followed by bone formation, while one with a larger diameter (0.35 mm) directly induced bone formation within the tunnels. It is concluded that the "vasculature-inducing geometry" of the carrier as an ECM is crucially important for osteogenesis.

[1]  A. Poole,et al.  Two distinctive BMP-carriers induce zonal chondrogenesis and membranous ossification, respectively; geometrical factors of matrices for cell-differentiation. , 1995, Connective tissue research.

[2]  A. Reddi Cell biology and biochemistry of endochondral bone development. , 1981, Collagen and related research.

[3]  T. Kohgo,et al.  Effects of geometry of hydroxyapatite as a cell substratum in BMP-induced ectopic bone formation. , 2000, Journal of biomedical materials research.

[4]  M. Luxoro,et al.  Electrophysiological Studies of Chilean Squid Axons under Internal Perfusion with Sodium-Rich Media , 1965, Science.

[5]  H. Takita,et al.  Pore size of porous hydroxyapatite as the cell-substratum controls BMP-induced osteogenesis. , 1997, Journal of biochemistry.

[6]  H. Takita,et al.  Regeneration of periodontal ligament and cementum by BMP-applied tissue engineering. , 1998, European journal of oral sciences.

[7]  A. Kirkbride,et al.  SINTERED POROUS HYDROXYAPATITES WITH INTRINSIC OSTEOINDUCTIVE ACTIVITY: GEOMETRIC INDUCTION OF BONE FORMATION , 1999 .

[8]  C. ANDREW L. BASSETT,et al.  Influence of Oxygen Concentration and Mechanical Factors on Differentiation of Connective Tissues in vitro , 1961, Nature.

[9]  M. Urist,et al.  Bone: Formation by Autoinduction , 1965, Science.

[10]  H. Takita,et al.  Geometry of Carriers Controlling Phenotypic Expression in BMP-Induced Osteogenesis and Chondrogenesis , 2001, The Journal of bone and joint surgery. American volume.

[11]  T. Kohgo,et al.  Geometric effect of matrix upon cell differentiation: BMP-induced osteogenesis using a new bioglass with a feasible structure. , 2001, Journal of biochemistry.

[12]  H. Ohgushi,et al.  BMP-induced osteogenesis on the surface of hydroxyapatite with geometrically feasible and nonfeasible structures: topology of osteogenesis. , 1998, Journal of biomedical materials research.