A novel construct has been developed to induce bone formation within a pedicle muscle flap. A critical size defect (20 × 15 mm 2 ) was created in the mandible of ten rabbits. The masseter muscle was adapted to fill the surgical defect and a combination of calcium sulphate/hydroxyapatite cement (CERAMENT™lSPINE SUPPORT), BMP-7 and rabbits' mesenchymal stromal cells (rMSCs) was injected into the muscle tissue. Bone regeneration was evaluated 3 months after surgery. Limited areas of bone formation anatomically bridged the defect, despite the new bone forming throughout the muscle and within the connective tissue surrounding the remnants of the cement. The bone was thicker in the bucco-lingual direction compared to the contra lateral (non-operated) side. Quantitative histomorphometry assessment showed that the average bone surface area was 21.2±6.0 mm 2 , this was significantly greater than that of the contra-lateral nonoperating control side. The calculated amounts of residual cement and soft tissue or spaces were 20±12% and 41±10%, respectively. The average mineral apposition rate (MAR) was 1.92 µm/day. The findings demonstrated the remarkable potential of the use of local muscle flaps for injectable bio-cement loaded with BMP and seeded with rMSCs to induce bone formation for the reconstruction of bony defects. Keywords: bone, Bioengineering, scaffolding, calcium sulphate Figure 1 Summary of the in-vitro and in-vivo research protocol. A) bone marrow aspiration from the posterior iliac crest; B) bone marrow aspirate ready for rMSCs isolation, expansion and culture; C) Cell suspension prepared for re-implantation in vivo, D) Dissection of the masseter muscle into superficial and deep layer; E) Creation of critical size defect of the ramus of the mandible; F) Adaptation of the masseter muscle into the defect and around the titanium plate; G) injection of the bio-cement; I) Osseo-induction under the effect of cement, BMP-7 and rMSCs; J) Ideal scenario of bone regeneration after 3 months.