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首页> 外文期刊>PLoS One >Circulating progenitor cells and the expression of Cxcl12 , Cxcr4 and angiopoietin-like 4 during wound healing in the murine ear
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Circulating progenitor cells and the expression of Cxcl12 , Cxcr4 and angiopoietin-like 4 during wound healing in the murine ear

机译:循环祖细胞和CxCl12,CXCR4和血管翅甙样4的鼠耳伤愈合期间的表达

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Migration of cells from both local and systemic sources is essential for the inflammatory and regenerative processes that occur during normal wound healing. CXCL12 is considered a critical regulator of CXCR4-positive cell migration during tissue regeneration. In this study, we investigated the expression of Cxcl12 and Cxcr4 during healing of a murine full thickness ear wound. We also investigated the expression of angiopoietin-like 4, which has been shown to participate in wound angiogenesis and reepithelialization. At time points up to 48hrs, complete blood counts were performed using automated hematology analysis, and the numbers of circulating stem and progenitor cells quantified using flow cytometry. Expression of both Cxcr4 and Angptl4 was significantly elevated within 3 days of wounding, and both were strongly expressed in cells of the epidermis. ANGPTL4 protein expression remained elevated in the epithelium through day 14. Cxcl12 expression was increased significantly at day 3, and remained elevated through day 21. Faint Cxcl12 staining was detectable in the epithelium at day 1, and thereafter staining was faint and more generalized. There were significantly fewer circulating total white blood cells and lymphocytes 1hr following ear punching. Similarly, there was a significant early (1hr) reduction in the number of circulating endothelial progenitor cells. Further studies are warranted to investigate whether ANGPTL4 and CXCL12/CXCR4 interact or synergize to facilitate cell recruitment and migration, and to potentiate reepithelialization and wound healing.
机译:来自局部和系统来源的细胞迁移对于正常伤口愈合期间发生的炎症和再生过程至关重要。 CXCL12被认为是组织再生期间CXCR4阳性细胞迁移的临界调节剂。在这项研究中,我们研究了在鼠全厚度耳伤期间CXCL12和CXCR4的表达。我们还研究了血管生成素的4的表达,其已被证明参与伤口血管生成和再皮脂化。在时间上至48小时,使用自动血液学分析进行完整的血液计数,以及使用流式细胞术定量的循环茎干和祖细胞的数量。 CXCR4和Angptl4的表达在伤口的3天内显着升高,两者都在表皮的细胞中强烈表达。通过第14天,上皮蛋白表达仍然持续升高。CXCl12表达在第3天显着增加,并且通过第21天保持升高。在第1天中,在上皮中检测到微弱的CXCl12染色,然后染色呈微弱,更广泛地呈现。耳朵冲压后,循环总白细胞和淋巴细胞循环总血细胞和淋巴细胞显着较少。类似地,循环内皮祖细胞的数量的显着早期(1Hr)降低。有必要进一步研究来调查AngptL4和CXCL12 / CXCR4是否相互作用或协同,以促进细胞招生和迁移,并提高再皮和伤口愈合。

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