## Abstract Stromal cell lines such as PA6 and MS5 have been employed for generating dopamine (DA) neurons from embryonic stem (ES) cells. The present study was designed to test whether bone marrow stromal cells (BMSC) derived from adult mice might be available as a feeder layer to produce DA cells
Mesenchymal stem cells accelerate bone allograft incorporation in the presence of diabetes mellitus
β Scribed by Eric A. Breitbart; Sharonda Meade; Vikrant Azad; Sloane Yeh; Loay Al-Zube; Yee-Shuan Lee; Joseph Benevenia; Treena Livingston Arinzeh; Sheldon S. Lin
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 355 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0736-0266
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β¦ Synopsis
Abstract
Allograft (Allo) incorporation in the presence of a systemic disease like diabetes mellitus (DM) is becoming a major issue in the orthopedic community. Mesenchymal stem cells (MSC) are multipotent stem cells that may be derived from adult, whole bone marrow and have been shown to induce bone formation in segmental defects when combined with the appropriate carrier/scaffold. The objectives of this study were to analyze the effect of DM upon Allo incorporation in a segmental rat femoral defect and to also investigate MSC augmentation of Allo incorporation. Segmental (5βmm) femoral defects were created in nonβDM and DM rats and treated with Allo containing demineralized bone matrix (DBM) or DBM with MSC augmentation. Histological scoring at 4 weeks demonstrated less mature bone in the DM/DBM group compared to its nonβDM counterpart (pβ<β0.001). However, there was significantly more mature bone in the DM/MSC group when compared to the DM/DBM group at both 4 and 8 weeks (pβ<β0.001 and pβ=β0.004). Furthermore, significantly more bone formation was observed in the DM/MSC group compared to the DM/DBM group at the 4βweek time point (pβ<β0.001). The results of this study suggest that MSC are a potential adjunct for bone regeneration when implanted in an orthotopic site in the presence of DM. Β© 2010 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 28:942β949, 2010
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