Akira Murayama1, Takashi Ajiki2, Yukinori Hayashi1, Katsushi Takeshita1. 1. Department of Orthopedic Surgery, Jichi Medical University, Tochigi, 329-0498, Japan. 2. Department of Orthopedic Surgery, Jichi Medical University, Tochigi, 329-0498, Japan. Electronic address: ajiki@jichi.ac.jp.
Abstract
BACKGROUND: Various types of artificial bone have been developed as alternatives to autologous bone grafts. In designing artificial bone, a porous structure is essential for the infiltration of blood and cells, which promotes angiogenesis within the bone matrix and ultimately ossification. However, it remains unclear what kind of pore system best promotes ossification. Here, we investigated angiogenesis in three different types of porous β-tricalcium phosphate (β-TCP) in a vascularized pedicle rat model. METHODS: Three types of porous β-TCP-β-TCP60 (60% porosity), β-TCP75 (75% porosity), and unidirectional porous β-tricalcium phosphate (UDPTCP; 57% porosity)-were examined. A cylindrical piece of artificial bone was implanted beneath the superficial inferior epigastric (SIE) vessels in the groin of rats and angiogenesis was allowed to occur. Two weeks after surgery, India ink or lectin was systemically injected to detect newly formed blood vessels originating from the SIE vessels. Immunohistochemistry for von Willebrand factor, α-smooth muscle actin, or type IV collagen was performed to clarify the structural features of the newly formed capillaries within the vascularized UDPTCP. RESULTS: The vascularity of the UDPTCP was superior to that of β-TCP60 and β-TCP75. The UDPTCP pore structure was completely filled with capillaries at 3 weeks after implantation. Immunohistochemistry showed that the walls of the capillaries contained endothelial cells, pericytes, and basement membrane originating from the SIE vessels, and that the cells proliferated and the basement membrane formed simultaneously as the newly formed capillaries extended through the unidirectional pore structure of the UDPTCP. CONCLUSIONS: UDPTCP had greater angiogenic potential than β-TCP60 and β-TCP75 in a vascularized pedicle rat model. Vascularized UDPTCP grafts may be an alternative to vascularized autologous bone grafts.
BACKGROUND: Various types of artificial bone have been developed as alternatives to autologous bone grafts. In designing artificial bone, a porous structure is essential for the infiltration of blood and cells, which promotes angiogenesis within the bone matrix and ultimately ossification. However, it remains unclear what kind of pore system best promotes ossification. Here, we investigated angiogenesis in three different types of porous β-tricalcium phosphate (β-TCP) in a vascularized pedicle rat model. METHODS: Three types of porous β-TCP-β-TCP60 (60% porosity), β-TCP75 (75% porosity), and unidirectional porous β-tricalcium phosphate (UDPTCP; 57% porosity)-were examined. A cylindrical piece of artificial bone was implanted beneath the superficial inferior epigastric (SIE) vessels in the groin of rats and angiogenesis was allowed to occur. Two weeks after surgery, India ink or lectin was systemically injected to detect newly formed blood vessels originating from the SIE vessels. Immunohistochemistry for von Willebrand factor, α-smooth muscle actin, or type IV collagen was performed to clarify the structural features of the newly formed capillaries within the vascularized UDPTCP. RESULTS: The vascularity of the UDPTCP was superior to that of β-TCP60 and β-TCP75. The UDPTCP pore structure was completely filled with capillaries at 3 weeks after implantation. Immunohistochemistry showed that the walls of the capillaries contained endothelial cells, pericytes, and basement membrane originating from the SIE vessels, and that the cells proliferated and the basement membrane formed simultaneously as the newly formed capillaries extended through the unidirectional pore structure of the UDPTCP. CONCLUSIONS:UDPTCP had greater angiogenic potential than β-TCP60 and β-TCP75 in a vascularized pedicle rat model. Vascularized UDPTCP grafts may be an alternative to vascularized autologous bone grafts.