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A study on the activity of dermal multipotent stem cells in initiation of wound repair

机译:真皮多能干细胞在创面修复中的活性研究

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Background: Wound healing is a process of cell-cell interaction and cell-extracellular matrix interaction. Dermal multipotent stem cells (dMSCs) have the abilities to promote survival and wound healing, but the potential function of dMSCs in wound healing, particularly in the initiation of wound repair, has not been fully understood. Methods: dMSCs and fibroblasts were isolated from neonatal rat dermis and were further purified and expanded. The cell cycles were determined with flow cytometry, while the radiosensitivity was measured by MTT assay. Rats were wounded with a 7-cm incision on the back skin and the wound fluids were collected by inserting two pieces of sterile polyvinyl alcohol sponge (1 cmin diameter and0.4 cmin thickness) subcutaneously into the dorsum of each rat through the midline of incision on the 1st, 2nd, 3rd and 4th day after incision. The effects of wound fluids on the proliferation of dMSCs and fibroblasts were measured with MTT assays. dMSC’s abilities of adhesion and attachment and its migration in response to wound fluids collected on the 1st day after incision were explored by measuring the percentage of floating cells and the cells migrated into wounding area in vitro, respectively. Results: The isolated dMSCs were morphologically homogenous and highly proliferative. Most of the cultured dMSCs were quiescent with few apoptotic cells. Compared with fibroblasts, dMSCs were more sensitive to radiation and more proliferative in response to wound fluids, especially to the wound fluids collected on the 1st day after wounding. Moreover, their abilities to attach, adhere and migrate were significantly enhanced with the early-phase wound fluids. Conclusions: As primitive stem cells, dMSCs are very responsive to wound fluids, which suggests dMSCs’ important role in wound healing, especially in initiating wound repair.
机译:背景:伤口愈合是细胞-细胞相互作用和细胞-细胞外基质相互作用的过程。皮肤多能干细胞(dMSCs)具有促进存活和伤口愈合的能力,但是尚未完全理解dMSCs在伤口愈合中的潜在功能,特别是在伤口修复的启动中。方法:从新生大鼠真皮中分离出dMSCs和成纤维细胞,并进一步纯化和扩增。用流式细胞术确定细胞周期,而通过MTT测定法测量放射敏感性。将大鼠的背部皮肤切成7厘米的切口,并通过切口中线将两片无菌聚乙烯醇海绵(直径1厘米,厚度0.4厘米)皮下插入每只大鼠的背部,收集伤口液在切口后的第1、2、3和4天。用MTT法测定伤口液对dMSCs和成纤维细胞增殖的影响。通过分别测量漂浮细胞的百分比和在体外迁移到伤口区域的细胞,探索dMSC对切口后第一天收集的伤口液的粘附和附着能力及其迁移。结果:分离的dMSCs在形态上同质并且高度增殖。多数培养的dMSCs静止,凋亡细胞很少。与成纤维细胞相比,dMSC对放射液更敏感,并且对伤口液尤其是伤口后第一天收集的伤口液的增殖性更高。而且,它们的附着,粘附和迁移能力随着早期伤口液的显着增强。结论:dMSCs作为原始干细胞,对伤口液非常敏感,这表明dMSCs在伤口愈合,尤其是在启动伤口修复中起着重要作用。

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