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源自羊水的胎儿组织工程。

Fetal tissue engineering from amniotic fluid.

作者信息

Kaviani Amir, Guleserian Kristine, Perry Tjörvi E, Jennings Russell W, Ziegler Moritz M, Fauza Dario O

机构信息

Department of Surgery, Children's Hospital and Harvard Medical School, 300 Longwood Avenue, Boston, MA 02115, USA.

出版信息

J Am Coll Surg. 2003 Apr;196(4):592-7. doi: 10.1016/s1072-7515(02)01834-3.

Abstract

BACKGROUND

We have recently shown, in an animal model, that amniotic fluid can be a source of cells for fetal tissue engineering. This study was aimed at determining whether fetal tissue constructs could also be engineered from cells normally found in human amniotic fluid.

STUDY DESIGN

Cells obtained from the amniotic fluid of pregnant women at 15 to 19 weeks of gestation (n=6) were cultured in Dulbecco's Modified Eagle's medium (Sigma Chemical, St Louis, MO) containing 20% fetal bovine serum and 5 ng/mL basic fibroblast growth factor in a 95% humidified, 5% CO(2) chamber at 37 degrees C. A subpopulation of morphologically distinct cells was then mechanically isolated from the rest and selectively expanded. The lineage of this subpopulation of amniocytes was determined by immunofluorescent staining with antibodies against standard intermediate filaments and surface antigens. Cell proliferation rates were determined by oxidation assay. After cell expansion, colonies of amniocytes were statically and dynamically seeded onto both unwoven, 1-mm-thick polyglycolic acid polymer scaffold and acellular human dermis for 72 hours. The resulting constructs were analyzed by scanning electron microscopy.

RESULTS

Amniocytes stained positively for smooth muscle actin, vimentin, cytokeratin 18, and fibroblast surface protein, and negatively for desmin, cluster of differentiation 31, and von Willebrand's factor (Dako, Carpenteria, CA). These findings are consistent with a mesenchymal, fibroblast-myofibroblast cell lineage. Mesenchymal amniocytes could be rapidly expanded in culture, based on results of the proliferation assay. Scanning electron microscopy of amniocyte constructs revealed dense, confluent layers of cells surrounding the polymer matrices and firm cell adhesion to both PGA and Alloderm (Lifecell Corp, Branchburg, NJ) scaffolds. No evidence of cell death was observed.

CONCLUSIONS

Subpopulations of fetal mesenchymal cells can be consistently isolated from human amniotic fluid and rapidly expanded in vitro. Human mesenchymal amniocytes attach firmly to both polyglycolic acid polymer and acellular human dermis. The amniotic fluid can be a valuable and practical cell source for fetal tissue engineering.

摘要

背景

我们最近在动物模型中表明,羊水可以作为胎儿组织工程的细胞来源。本研究旨在确定胎儿组织构建物是否也可以由人羊水中正常存在的细胞构建而成。

研究设计

从妊娠15至19周孕妇的羊水中获取细胞(n = 6),在含有20%胎牛血清和5 ng/mL碱性成纤维细胞生长因子的杜尔贝科改良伊格尔培养基(西格玛化学公司,密苏里州圣路易斯)中,于37℃、95%湿度、5%二氧化碳培养箱中培养。然后从其余细胞中机械分离出形态不同的细胞亚群并选择性扩增。通过用针对标准中间丝和表面抗原的抗体进行免疫荧光染色来确定该羊膜细胞亚群的谱系。通过氧化测定法确定细胞增殖率。细胞扩增后,将羊膜细胞集落静态和动态接种到1毫米厚的无纺聚乙醇酸聚合物支架和脱细胞人真皮上72小时。通过扫描电子显微镜分析所得构建物。

结果

羊膜细胞平滑肌肌动蛋白染色呈阳性,波形蛋白、细胞角蛋白18和成纤维细胞表面蛋白染色也呈阳性,结蛋白、分化簇31和血管性血友病因子染色呈阴性(达科公司,加利福尼亚州卡彭特里亚)。这些发现与间充质、成纤维细胞 - 肌成纤维细胞谱系一致。基于增殖测定结果,间充质羊膜细胞在培养中可快速扩增。羊膜细胞构建物的扫描电子显微镜显示聚合物基质周围有密集、汇合的细胞层且细胞与聚乙醇酸和异体细胞真皮(生命细胞公司,新泽西州布兰奇堡)支架牢固黏附。未观察到细胞死亡迹象。

结论

胎儿间充质细胞亚群可从人羊水中持续分离并在体外快速扩增。人羊膜间充质细胞与聚乙醇酸聚合物和脱细胞人真皮都牢固黏附。羊水可以成为胎儿组织工程有价值且实用的细胞来源。

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