分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

Maintaining Inducibility of Dermal Follicle Cells on Silk Fibroin/Sodium Alginate Scaffold for Enhanced Hair Follicle Regeneration

Kuo Dong, Xinyu Wang, Ying Shen, Yiyu Wang, Binbin Li, Cuiling Cai, Linyi Shen, Yajin Guo

Journal:Biology-Basel

IF:5.08

DOI:10.3390/biology10040269

PMID:33810528

Published:2021-03-26

research field:肿瘤学分子生物学细胞生物学

Abstract

Simple SummaryPatients with severe skin damage need to transplant artificial skin substitutes to achieve repair, and often the repaired part cannot achieve the regeneration of accessory organs such as hair follicles. It is very important to study artificial skin substitutes that can promote the regeneration of hair follicles. Dermal papilla cells in hair follicles can express a variety of growth factors, which play an important role in the growth of hair follicles. Dermal papilla cells were used as seed cells and cultured with a biomimetic silk fibroin/sodium alginate scaffold similar to the extracellular matrix around the dermal papilla to explore cell-compatibility on the scaffold. Our research found that a silk fibroin/sodium alginate scaffold is a good biomimetic of the extracellular matrix structure, and that the dermal papilla cells could maintain normal morphology and aggregate growth characteristics on the scaffold. We then proved through animal experiments that this scaffold can promote skin repair and induce hair follicle regeneration.AbstractThe extracellular matrix (ECM) is important for maintaining cell phenotype and promoting cell proliferation and differentiation. In order to better solve the problem of skin appendage regeneration, a combination of mechanical/enzymatic digestion methods was used to self-extract dermal papilla cells (DPCs), which were seeded on silk fibroin/sodium alginate scaffolds as seed cells to evaluate the possibility of skin regeneration/regeneration of accessory organs. Scanning electron microscopy (SEM) graphs showed that the interconnected pores inside the scaffold had a pore diameter in the range of 153–311 μm and a porosity of 41–82%. Immunofluorescence (IF) staining and cell morphological staining proved that the extracted cells were DPCs. The results of a Cell Counting Kit-8 (CCK-8) and Calcein-AM/PI live-dead cell staining showed that the DPCs grew well in the composite scaffold extract. Normal cell morphology and chara

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