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纤维蛋白浓度对体外表皮真皮等同物生成的影响。

Effect of Fibrin Concentration on the In Vitro Production of Dermo-Epidermal Equivalents.

机构信息

Department of Bioengineering and Aerospace Engineering, Universidad Carlos III de Madrid (UC3M), 28903 Madrid, Spain.

Instituto de Investigación Sanitaria Gregorio Marañón, 28007 Madrid, Spain.

出版信息

Int J Mol Sci. 2021 Jun 23;22(13):6746. doi: 10.3390/ijms22136746.

Abstract

Human plasma-derived bilayered skin substitutes were successfully used by our group to produce human-based in vitro skin models for toxicity, cosmetic, and pharmaceutical testing. However, mechanical weakness, which causes the plasma-derived fibrin matrices to contract significantly, led us to attempt to improve their stability. In this work, we studied whether an increase in fibrin concentration from 1.2 to 2.4 mg/mL (which is the useful fibrinogen concentration range that can be obtained from plasma) improves the matrix and, hence, the performance of the in vitro skin cultures. The results show that this increase in fibrin concentration indeed affected the mechanical properties by doubling the elastic moduli and the maximum load. A structural analysis indicated a decreased porosity for the 2.4 mg/mL hydrogels, which can help explain this mechanical behavior. The contraction was clearly reduced for the 2.4 mg/mL matrices, which also allowed for the growth and proliferation of primary fibroblasts and keratinocytes, although at a somewhat reduced rate compared to the 1.2 mg/mL gels. Finally, both concentrations of fibrin gave rise to organotypic skin cultures with a fully differentiated epidermis, although their lifespans were longer (25-35%) in cultures with more concentrated matrices, which improves their usefulness. These systems will allow the generation of much better in vitro skin models for the testing of drugs, cosmetics and chemicals, or even to "personalized" skin for the diagnosis or determination of the most effective treatment possible.

摘要

我们小组成功地使用人血浆衍生的双层皮肤替代物来制备基于人体的体外皮肤模型,用于毒性、化妆品和药物测试。然而,由于机械强度不足,导致血浆衍生的纤维蛋白基质显著收缩,因此我们试图提高其稳定性。在这项工作中,我们研究了将纤维蛋白浓度从 1.2 增加到 2.4mg/mL(这是可以从血浆中获得的有用纤维蛋白原浓度范围)是否可以改善基质,从而改善体外皮肤培养物的性能。结果表明,这种纤维蛋白浓度的增加确实通过将弹性模量和最大负载增加一倍来影响机械性能。结构分析表明,2.4mg/mL 水凝胶的孔隙率降低,这可以帮助解释这种机械行为。2.4mg/mL 基质的收缩明显减少,这也允许原代成纤维细胞和角质形成细胞的生长和增殖,尽管与 1.2mg/mL 凝胶相比,其增殖速度略有降低。最后,两种浓度的纤维蛋白都产生了具有完全分化表皮的器官型皮肤培养物,尽管在纤维蛋白浓度更高的培养物中,它们的寿命更长(25-35%),这提高了它们的有用性。这些系统将允许生成更好的体外皮肤模型,用于测试药物、化妆品和化学品,甚至可以“个性化”皮肤,以进行诊断或确定最有效的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17c/8269027/bf0c77ab5af4/ijms-22-06746-g001.jpg

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