Suppr超能文献

人毛囊真皮乳头细胞在软 3D 自组装肽支架中的培养和分化。

Culture and Differentiation of Human Hair Follicle Dermal Papilla Cells in a Soft 3D Self-Assembling Peptide Scaffold.

机构信息

Tissue Engineering Research Laboratory, Department of Bioengineering, IQS-School of Engineering, Ramon Llull University, 08017 Barcelona, Spain.

出版信息

Biomolecules. 2020 Apr 28;10(5):684. doi: 10.3390/biom10050684.

Abstract

Hair follicle dermal papilla cells (HFDPC) are a specialized cell population located in the bulge of the hair follicle with unique characteristics such as aggregative behavior and the ability to induce new hair follicle formation. However, when expanded in conventional 2D monolayer culture, their hair inductive potency is rapidly lost. Different 3D culture techniques, including cell spheroid formation, have been described to restore, at least partially, their original phenotype, and therefore, their hair inductive ability once transplanted into a recipient skin. Moreover, hair follicle dermal papilla cells have been shown to differentiate into all mesenchymal lineages, but their differentiation potential has only been tested in 2D cultures. In the present work, we have cultured HFDPC in the 3D self-assembling peptide scaffold RAD16-I to test two different tissue engineering scenarios: restoration of HFDPC original phenotype after cell expansion and osteogenic and adipogenic differentiation. Experimental results showed that the 3D environment provided by RAD16-I allowed the restoration of HFDPC signature markers such as alkaline phosphatase, versican and corin. Moreover, RAD16-I supported, in the presence of chemical inductors, three-dimensional osteogenic and adipogenic differentiation. Altogether, this study suggests a potential 3D culture platform based on RAD16-I suitable for the culture, original phenotype recovery and differentiation of HFDPC.

摘要

毛囊真皮乳头细胞(HFDPC)是一种位于毛囊隆起处的特化细胞群体,具有独特的特性,如聚集行为和诱导新的毛囊形成的能力。然而,当在常规的二维单层培养中进行扩增时,其毛发诱导能力会迅速丧失。不同的三维培养技术,包括细胞球体形成,已经被描述为至少部分地恢复其原始表型,因此,一旦将其移植到受体皮肤中,其毛发诱导能力就会恢复。此外,毛囊真皮乳头细胞已被证明可以分化为所有间充质谱系,但它们的分化潜能仅在二维培养中进行了测试。在本工作中,我们将 HFDPC 培养在 3D 自组装肽支架 RAD16-I 中,以测试两种不同的组织工程方案:细胞扩增后 HFDPC 原始表型的恢复和成骨和成脂分化。实验结果表明,RAD16-I 提供的 3D 环境允许恢复 HFDPC 的特征标志物,如碱性磷酸酶、软骨寡聚基质蛋白和心钠肽。此外,RAD16-I 在化学诱导剂的存在下支持三维成骨和成脂分化。总之,这项研究提出了一种基于 RAD16-I 的潜在的 3D 培养平台,适用于 HFDPC 的培养、原始表型的恢复和分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d872/7277435/9e826f814d2d/biomolecules-10-00684-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验