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源自兔的脂肪前体细胞在体外具有成骨潜能。

Leporine-derived adipose precursor cells exhibit in vitro osteogenic potential.

作者信息

Dudas Jason R, Losee Joseph E, Penascino Virginia M, Smith Darren M, Cooper Gregory M, Mooney Mark P, Jiang Shao, Rubin J Peter, Marra Kacey G

机构信息

Division of Plastic Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

出版信息

J Craniofac Surg. 2008 Mar;19(2):360-8. doi: 10.1097/SCS.0b013e318163e17b.

Abstract

Adipose-derived stem cells (ASCs) possess osteogenic potential and have been shown to undergo in vitro osteoblastic differentiation and promote bone regeneration in vivo. In this study, we describe the isolation and osteoblastic differentiation of rabbit ASCs and their behavior on a gelatin foam scaffold. These studies will form the basis of future in vivo studies of the osteogenic potential of rabbit ASCs for calvarial defect repair.Adipose-derived stem cells were isolated from New Zealand White rabbits and cultured in osteogenic medium +/- bone morphogenetic protein 2. Osteoblastic differentiation was assessed via histochemical stains for alkaline phosphatase (AP) and extracellular matrix (ECM) calcification. Reverse transcriptase polymerase chain reaction was performed to evaluate the expression of AP and the osteogenic transcription factor Runx2. Adipose-derived stem cells were seeded onto gelatin foam scaffolds at various densities, and cell proliferation was measured fluorometrically. Cells isolated from rabbit adipose tissue exhibited classic ASC morphology. Adipose-derived stem cells cultured in osteogenic medium exhibited more robust staining for AP and ECM calcification compared with ASCs in control medium. Furthermore, this staining was more marked in male ASCs versus female ASCs and also enhanced by bone morphogenetic protein 2. mRNA for AP and Runx2 were also increased in the osteoinduced cells. Theoptimal seeding density was 1 x 10 ASCs on an 8-mm gelatin foam scaffold. We have shown that rabbit ASCs have in vitro osteogenic potential and are compatible with a gelatin foam scaffold. Characteristic features of osteoblasts, such as ECM mineralization and expression of osteogenic genes, were demonstrated in this cell population. In vitro osteoblastic differentiation and scaffold studies are necessary before in vivo trials. The mechanism underlying the sex-based variation in osteoblastic differentiation is unknown but may involve signaling via factors such as estrogen.

摘要

脂肪来源干细胞(ASCs)具有成骨潜能,已被证明可在体外发生成骨细胞分化,并在体内促进骨再生。在本研究中,我们描述了兔ASCs的分离、成骨细胞分化及其在明胶海绵支架上的行为。这些研究将为未来关于兔ASCs修复颅骨缺损成骨潜能的体内研究奠定基础。从新西兰白兔中分离脂肪来源干细胞,并在添加或不添加骨形态发生蛋白2的成骨培养基中培养。通过碱性磷酸酶(AP)和细胞外基质(ECM)钙化的组织化学染色评估成骨细胞分化。进行逆转录聚合酶链反应以评估AP和成骨转录因子Runx2的表达。将脂肪来源干细胞以不同密度接种到明胶海绵支架上,并用荧光法测量细胞增殖。从兔脂肪组织分离的细胞表现出典型的ASC形态。与对照培养基中的ASCs相比,在成骨培养基中培养的脂肪来源干细胞对AP和ECM钙化的染色更强。此外,这种染色在雄性ASCs中比雌性ASCs更明显,并且也被骨形态发生蛋白2增强。在成骨诱导细胞中,AP和Runx2的mRNA也增加。最佳接种密度是在8毫米明胶海绵支架上接种1×10个ASCs。我们已经证明兔ASCs具有体外成骨潜能,并且与明胶海绵支架相容。在该细胞群体中证明了成骨细胞的特征,如ECM矿化和成骨基因的表达。在进行体内试验之前,体外成骨细胞分化和支架研究是必要的。成骨细胞分化中基于性别的差异的潜在机制尚不清楚,但可能涉及雌激素等因子的信号传导。

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