脂肪工程骨:脂肪来源干细胞介导的骨再生的体内机制综述

IF 5 Q1 ENGINEERING, BIOMEDICAL Progress in biomedical engineering (Bristol, England) Pub Date : 2021-01-01 DOI:10.1088/2516-1091/ac1522
Allison L Horenberg, Alexandra N. Rindone, W. Grayson
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引用次数: 4

摘要

脂肪源性基质/干细胞(ASCs)由于其易于分离、丰富和成骨能力,具有促进骨再生的巨大潜力。然而,尽管经过二十年的研究,对其体内骨再生能力的确切机制的研究仍然存在矛盾。具体来说,有多篇报道表明,骨再生的直接机制(即ASCs直接分化成成骨细胞并形成新的骨基质)或间接机制(即ASCs通过其分泌特征刺激内源性细胞)。为了解决这一差异,我们批判性地回顾了利用ASCs进行体内骨再生的研究,并采用了跟踪细胞命运的方法。我们通过检查特定缺陷和使用的动物模型、细胞分选或预处理方法、细胞剂量和细胞存活/分布数据的定量评估来评估个体研究的严谨性,以确定其主张的强度。有强有力的证据支持ASCs的直接分化和基于分泌因子(成骨/血管生成、免疫调节或细胞外基质因子)的间接信号传导,这表明ASCs的促再生能力是多种因素共同作用的结果。然而,关于移植后ASC植入的精确效率,ASC与宿主细胞在不同愈合阶段发生的时空相互作用类型,破骨细胞,神经和免疫细胞对ASC介导的再生的贡献,仍然存在显着的知识空白。新兴技术将进一步阐明ASCs在骨再生中的具体作用机制。
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Engineering bone from fat: a review of the in vivo mechanisms of adipose derived stem cell-mediated bone regeneration
Adipose-derived stromal/stem cells (ASCs) have considerable potential to promote bone regeneration due to their ease of isolation, abundance, and osteogenic capacity. However, despite two decades of research, studies of the precise mechanisms underlying their in vivo osteo-regenerative capacity remain contradictory. Specifically, there are multiple reports that suggest either a direct mechanism (i.e. ASCs directly differentiate into osteoblasts and lay done new bone matrix) or an indirect mechanism (i.e. ASCs stimulate endogenous cells via their secretory profiles) of bone regeneration. To address this discrepancy we critically reviewed studies utilizing ASCs for in vivo bone regeneration and employed methods to track cell fate. We evaluated the rigor of individual studies by examining the specific defect and animal models employed, cell sorting or pretreatment methods, and quantitative assessments of cell dosing and cell survival/distribution data to determine the strength of their claims. There is robust evidence to support both a direct differentiation of ASCs and indirect signaling based on secreted factors: osteogenic/angiogenic, immunomodulatory, or extracellular matrix factors, suggesting that a combination of factors underlie the pro-regenerative capacity of ASCs. However, there remains significant knowledge gaps regarding the precise efficiency of ASC engraftment following transplantation, the types of spatiotemporal interactions that occur between ASCs and host cells during the different stages of healing, and the contributions of osteoclasts, nerves, and immune cells to ASC-mediated regeneration. Emerging technologies will enable further elucidation of the specific mechanisms of action of ASCs in bone regeneration.
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