Miura et al. intentionally induced spontaneous immortalization after numerous passages (P29 to P54) and demonstrated the contribution of the transformed cells to fibrosarcoma formation in vivo [95]. We

have also confirmed sarcoma formation by cultured murine compact bone-derived MSCs ( Fig. 3). Rubio et al. showed that, although MSCs can be managed safely during the standard ex vivo expansion period (six to eight weeks), human MSCs can undergo spontaneous transformation following long-term in vitro culture (four to five months), and the transformed cells lead to the formation of tumors in mice [97]. This information indicates that unmodified MSCs should be used Torin 1 at early passages to avoid potential chromosomal abnormalities that result from long-term culture. Additionally, it has been recommended by the Food and Drug Administration (FDA) that “minimally manipulated” cells be used for human clinical trials. In this regard, attempts are being made to develop an efficient production system to produce clinically relevant numbers of hMSCs in relatively shorter periods of time with lower passage numbers [98]. As adult stem cells, MSCs, are free from ethical concerns, residents

of multiple tissues, able to efficiently differentiate along an osteogenic lineage and can be used as vehicles for bone gene therapy. These characteristics make MSCs promising candidates check details for use in bone engineering and regeneration. Unfortunately, to date, no markers have yet been identified that specifically identify MSCs and it is difficult to culture MSCs in chemically-defined media. Additionally, while the characteristics of multipotency and autonomous growth are suitable for producing qualified cells for tissue regeneration, at the same time, these characteristics are very close to those of tumorigenesis. Therefore, regarding clinical use, this review

did not reach any significant conclusions as to the most promising model for MSC reconstruction. However, this review does show the need Sitaxentan for additional collaborative studies using similar designs and data analysis in advancing the science of bone reconstruction using MSCs. The authors have no conflicts of interest to declare. This work was supported in part by a Grant-in-Aid for funding scientific research from the Ministry of Education, Culture, Sports, Science and Technology of Japan. “
“Bone loss in the maxillo-facial region is a major health care concern. Maintaining the integrity of the bone structure around the teeth or dental implants is crucial for preserving oral function. Alveolar cleft repairs and maxillary defect reconstruction after tumor surgeries are also challenging requirements, as they need to be designed to meet specific needs and demands for optimizing functional and cosmetic outcomes.