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Mixed enzymatic-explant protocol for isolation of mesenchymal stem cells from Wharton’s jelly and encapsulation in 3D culture system

机译:混合酶-外植体方案可从沃顿氏胶冻中分离间充质干细胞并封装在3D培养系统中

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We report combination of explants and enzymatic protocol as mixed enzymatic-explant procedure to faster extraction of MSCs from WJ. Umbilical cords (UC) were collected from Imam Khomini Hospital. For explant outgrowth, 6 - 9 pieces of WJ were transferred onto tissue culture flask and waited for attachment. For mixed enzymatic-explant, 1 cm3 pieces WJ were placed in enzymatic cocktail comprising 4 mg/ml Collagenase Type I and 1 mg/ml Hyaluronidase and 0.1% trypsin-EDTA. Then isolated cells were analyzed for surface cell markers such as CD73, CD31. Isolated 1.0 × 106 MSCs/ml were encapsulated in alginate hydrogel. Cells with MSCs phenotype were isolated from mixed enzymatic-explant and explant procedures within 24 - 48 hrs and 7 - 10 days, respectively. Both of procedures were shown to form clumps and colonies with dense centers. Phenotypic changes gradually appeared as round cell in UC pieces into homogeneous spindle-shaped and typical fibroblast-like shape cells. By using flow cytometery MSCs showed positive for CD73, and negative for CD31. the morphology of viable MSCs in the beads did not significantly show a different morphology pattern before and after the bead formation process. These findings are indicated that when mixed enzymatic-explant procedure is performed MSCs can be isolated faster and much higher from WJ. These finding is important in comparing with time consuming explants culture for isolation of MSCs.
机译:我们报告外植体和酶协议的组合作为混合酶-外植程序以更快地从WJ提取MSC。脐带(UC)从伊玛目科米尼医院(Imam Khomini Hospital)收集。对于外植体生长,将6-9片WJ转移到组织培养瓶中,等待附着。对于混合的酶促外植体,将1 cm3块WJ置于包含4 mg / ml I型胶原酶和1 mg / ml透明质酸酶和0.1%胰蛋白酶-EDTA的酶混合物中。然后分析分离的细胞的表面细胞标志物,例如CD73,CD31。将分离的1.0×106 MSCs / ml封装在藻酸盐水凝胶中。分别在24-48小时和7-10天之内从混合酶促外植和外植过程中分离出具有MSCs表型的细胞。两种方法均显示出形成团块和具有密集中心的菌落。表型改变逐渐以UC细胞中的圆形细胞形式出现,形成均匀的纺锤形和典型的成纤维细胞样形状的细胞。通过流式细胞术,MSC对CD73显示阳性,而对CD31显示阴性。珠子中存活的MSC的形态在珠子形成之前和之后没有明显显示出不同的形态模式。这些发现表明,当进行混合酶-外植程序时,可以更快地从WJ中分离出MSC,并且分离得更高。这些发现与将耗时的外植体培养物用于分离MSC相比具有重要意义。

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