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优化视黄酸刺激以促进小鼠脂肪来源的成年基质细胞的成骨分化

Refining retinoic acid stimulation for osteogenic differentiation of murine adipose-derived adult stromal cells.

作者信息

Wan Derrick C, Siedhoff Matthew T, Kwan Matthew D, Nacamuli Randall P, Wu Benjamin M, Longaker Michael T

机构信息

Department of Surgery, School of Medicine, Stanford University, Stanford, California 94305-5148, USA.

出版信息

Tissue Eng. 2007 Jul;13(7):1623-31. doi: 10.1089/ten.2006.0283.

Abstract

Murine adipose-derived adult stromal cells (ADAS) seeded onto appropriate scaffolds and pre-incubated with retinoic acid have been shown to generate in vivo bone rapidly. Prompt resorption ensues, however, as a result of osteoclastogenesis, likely secondary to retinoic acid carryover. In this study, we determined the effects of abbreviated retinoic acid exposure on ADAS osteogenic differentiation. Histological staining and gene expression analysis revealed that longer retinoic acid exposure resulted in better in vitro bone differentiation. However, significant osteogenesis was observed in ADAS after just 15 days of retinoic acid supplementation, suggesting that continual culture with retinoic acid is unnecessary for initiation of the osteogenic program. This was confirmed using ADAS pre-incubated in monolayer with an abbreviated 15 days of retinoic acid exposure before implantation into critical-sized calvarial defects. Similar rates of regeneration were observed between ADAS exposed to for 15 days or for a full 25-day course of retinoic acid before defect repair. Furthermore, by limiting retinoic acid exposure to ADAS in monolayer without scaffold, accelerated bone formation was observed without concomitant osteoclastic resorption. These data suggest that skeletal regeneration may be improved by modulating retinoic acid exposure before implantation, markedly accelerating the repair of bone defects using ADAS.

摘要

已证明,接种到合适支架上并与视黄酸预孵育的小鼠脂肪来源的成体基质细胞(ADAS)能在体内快速生成骨组织。然而,由于破骨细胞生成,可能继发于视黄酸残留,随后会迅速发生吸收。在本研究中,我们确定了缩短视黄酸暴露时间对ADAS成骨分化的影响。组织学染色和基因表达分析表明,较长时间的视黄酸暴露导致更好的体外骨分化。然而,在补充视黄酸仅15天后,ADAS中就观察到显著的成骨,这表明启动成骨程序无需持续用视黄酸培养。将在单层中预孵育15天缩短视黄酸暴露时间的ADAS植入临界大小的颅骨缺损后,证实了这一点。在缺损修复前,暴露于视黄酸15天或完整25天疗程的ADAS之间观察到相似的再生率。此外,通过在无支架的单层中限制ADAS对视黄酸的暴露,观察到骨形成加速且无伴随的破骨细胞吸收。这些数据表明,通过在植入前调节视黄酸暴露,可改善骨骼再生,显著加速使用ADAS修复骨缺损。

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