Abstract:Objective To evaluate the effect of hydroxyapatite-gelatin (HAP-GEL) scaffold prepared by 3D printing technique combined with bone marrow mesenchymal stem cells (BMSCs) and human umbilical vein endothelial cells (HUVECs) in repairing rabbit skull defect with histopathological method. Methods The 3D printed HAP-GEL scaffolds were co-cultured with BMSCs and HUVECs to construct tissue-engineered bone. Twenty-four New Zealand white rabbits were randomly divided into HAP-GEL scaffolds group, HAP-GEL scaffolds + BMSCs and HUVECs group, blank control group and positive control group with 6 rabbits in each group. The 3D printed HAP-GEL scaffolds or HAP-GEL scaffolds combined with BMSCs and HUVECs were randomly implanted in the defect area. The autogenous skull was set as positive control, and the blank defect was set as negative control. Bone healing was analyzed by histopathological observation at 4 and 12 weeks after modeling. Results Microscopically, no acute or chronic inflammatory cell infiltration was found in all groups. HE staining showed that 4 weeks after operation, only a small amount of fibrous connective tissue was formed in the blank control group, while a small amount of new bone was formed in the HAP-GEL scaffolds group. Besides, part of the new bone began to fuse in the HAP-GEL scaffolds + BMSCs and HUVECs group, and the new bone mass was similar to that in the positive control group. At 12 weeks after operation, there was little new bone mass in the blank control group, and the new bone in the HAP-GEL scaffolds group was lamellar-shaped. In addition, the defect area in the HAP-GEL scaffolds + BMSCs and HUVECs group was almost filled with new bone, the mass of which was significantly more than that in the former two groups and similar to that in the positive control group. Masson’s trichrome staining showed that 4 weeks after operation, only a small amount of fibrous tissue was found in the blank control group. Blue-stained new bone and a small amount of red-stained mature bone were formed in the HAP-GEL scaffolds group, but the staining was faintly colored. In the HAP-GEL scaffolds + BMSCs and HUVECs group, the area of red-stained mature bone was larger than that in the HAP-GEL scaffolds group, and the repairing effect was similar to that in the positive control group. At 12 weeks after operation, blue-stained new bone appeared in the blank control group as shown in Masson’s trichrome staining. The mature bone area in the HAP-GEL scaffolds group was further enlarged, and the scaffolds were segmented, wrapped and absorbed. In the HAP-GEL scaffolds + BMSCs and HUVECs group, a large area of red-stained mature bone was formed, mixed with a small amount of blue-stained new bone, with a small amount of scaffold remained, and the osteogenic effect was similar to that of the positive control group but better than that of the HAP-GEL scaffolds group and the blank control group. Conclusions The 3D printed HAP-GEL scaffold combined with BMSCs and HUVECs exhibited great efficacy in repairing skull defects in rabbits.