首页> 外文会议>International Symposium of Biomedical Engineering >Cito-Compability Analysis of Mesenchymal Stem Cells in Platelet Rich Fibrin Matrix (PRFM) for Tissue Regeneration
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Cito-Compability Analysis of Mesenchymal Stem Cells in Platelet Rich Fibrin Matrix (PRFM) for Tissue Regeneration

机译:血小板富纤维蛋白基质(PRFM)中间充质干细胞组织再生的富含钙合理分析

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Mesenchymal stem cells (MSCs) is progenitor cell that capable to differentiate to various mesenchymal or non-mesenchymal lineages. MSC also play a role towards injury during healing and regeneration processes in most tissue. Platelet rich plasma (PRP) had been reported to induce endometrium regeneration, therefore a compacted form of PRP, known as platelet rich fibrin matrix (PRFM), was studied for its capability to host MSC and the behavior of MSC in the matrix. PRP gelation was generated by adding 25 mM of CaCl_2 to form a coin shape with diameter of 5 cm. Each matrix was cut into half, seeded directly with bone marrow (hBM-MSC) and umbilical cord MSC (hUC-MSC) with seeding density of 2,000 cell.cm~(-2). Initial cellular attachment was analyzed using H&E staining, while the cellular viability was assessed quantitatively using MTT assay and qualitatively using Live/Dead staining. hUC-MSC showed the highest viability compared to hBM-MSC when delivered in PRFM, especially during the first and five days incubation. After 10 dan 15 days incubation, the viability had dropped. The Live/Dead staining indicated too crowded population and most cells were dead. This might be due to asphyxia. hUC-MSC and hBM-MSC were seen to proliferated and infiltrated the PRFM over the time, although the ratio of dead cells was more dominant in the later day of incubation. PRFM can be used to deliver MSC to the site injury. However the direct seeding method was not optimal to hold the cells on place during the first 24 h incubation because they were easily detached.
机译:间充质干细胞(MSCs)是能够区分各种间充质或非间充质谱系的祖细胞。 MSC在大多数组织中,在愈合和再生过程中也发挥了伤害。据报道血小板富血浆(PRP)诱导子宫内膜再生,因此研究了一种称为血小板纤维蛋白基质(PRFM)的PRP的压实形式,以宿主MSC和MSC在基质中的行为。通过加入25mm的CaCl_2来产生PRP凝胶,以形成直径为5cm的硬币形状。将每种基质切成一半,直接用骨髓(HBM-MSC)和脐带MSC(HUC-MSC)接种,播种密度为2,000个细胞.CM〜(-2)。使用H&E染色分析初始细胞附着,而使用MTT测定和使用活/死染料定量评估细胞活力。与HBM-MSC相比,HUC-MSC在PRFM中递送时,可获得最高的活力,特别是在第一次和5天孵育期间。 10 DAN 15天孵育后,生存能力掉了下来。现场/死亡染色表明人口过于拥挤,大多数细胞都死了。这可能是由于窒息。 HUC-MSC和HBM-MSC被视为增殖和渗透到PRFM随着时间的推移,尽管死细胞的比例在孵育后的后期更占主导地位。 PRFM可用于将MSC提供给站点损伤。然而,在前24小时孵育期间,直接播种方法不适用于将细胞保持在适当位置,因为它们很容易拆卸。

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