Buss Leonardo Fernandes, de Martin Gustavo Sigrist, Martinez Elizabeth Ferreira, Filgueiras Isabela Amanda de Abreu Araújo Porcaro, Magnabosco José Luiz, Alves Bruno Frenhan, de Macedo Almeida Bruno, Kotaka Tatiana, Teixeira Marcelo Lucchesi, Ferreira José Ricardo Muniz, Rocha Daniel Navarro da, Canal Raul, Aloise Antonio Carlos, Holliday Lexie Shannon, Pelegrine André Antonio
Faculdade de Odontologia São Leopoldo Mandic, Campinas 13045-755, SP, Brazil.
Division of Cell Biology, Faculdade São Leopoldo Mandic, Campinas 13045-755, SP, Brazil.
J Funct Biomater. 2023 Jul 25;14(8):396. doi: 10.3390/jfb14080396.
The aim of this study was to test whether lyophilized conditioned media from human dental pulp mesenchymal stem cell cultures promote the healing of critical-size defects created in the calvaria of rats. Prior to the surgical procedure, the medium in which dental pulp stem cells were cultured was frozen and lyophilized. After general anesthesia, an 8 mm diameter bone defect was created in the calvaria of twenty-four rats. The defects were filled with the following materials: xenograft alone (G1) or xenograft associated with lyophilized conditioned medium (G2). After 14 or 42 days, the animals were euthanized, and the specimens processed for histologic and immunohistochemical analysis. Bone formation at the center of the defect was observed only in the G2 at 42 days. At both timepoints, increased staining for VEGF, a marker for angiogenesis, was observed in G2. Consistent with this, at 14 days, G2 also had a higher number of blood vessels detected by immunostaining with an anti-CD34 antibody. In conclusion, conditioned media from human dental pulp mesenchymal stem cell cultures had a positive effect on the regenerative process in rat critical-size bone defects. Both the formation of bone and enhancement of vascularization were stimulated by the conditioned media.
本研究的目的是测试人牙髓间充质干细胞培养物的冻干条件培养基是否能促进大鼠颅骨临界尺寸骨缺损的愈合。在手术前,将培养牙髓干细胞的培养基冷冻并冻干。全身麻醉后,在24只大鼠的颅骨上制作直径8毫米的骨缺损。缺损用以下材料填充:单纯异种移植物(G1)或与冻干条件培养基联合的异种移植物(G2)。14天或42天后,对动物实施安乐死,并对标本进行组织学和免疫组织化学分析。仅在42天时在G2组缺损中心观察到骨形成。在两个时间点,G2组中血管生成标志物VEGF的染色均增加。与此一致的是,在14天时,用抗CD34抗体免疫染色检测到G2组的血管数量也更多。总之,人牙髓间充质干细胞培养物的条件培养基对大鼠临界尺寸骨缺损的再生过程有积极作用。条件培养基刺激了骨形成和血管生成增强。