In vitro effects of wool-derived keratin on human dental pulp-derived stem cells for endodontic applications

被引:4
|
作者
Sharma, Lavanya Ajay [1 ]
Ramesh, Niranjan [2 ]
Sharma, Ajay [1 ]
Ratnayake, Jithendra T. B. [3 ]
Love, Robert M. [1 ]
Alavi, Seyed Ebrahim [1 ]
Wilson, Megan J. [2 ]
Dias, George J. [2 ]
机构
[1] Griffith Univ, Sch Med & Dent, Gold Coast, Qld, Australia
[2] Univ Otago, Sch Biomed Sci, Dept Anat, Dunedin, New Zealand
[3] Univ Otago, Fac Dent, Dept Oral Sci, Dunedin, New Zealand
来源
BRITISH JOURNAL OF ORAL & MAXILLOFACIAL SURGERY | 2023年 / 61卷 / 09期
关键词
Keratin; Human dental pulp stem cells; Endodontics; Cell growth; Cell differentiation; Tissue engineering; HUMAN HAIR; SCAFFOLDS; DIFFERENTIATION; MINERALIZATION; REGENERATION; FABRICATION; SPONGE; TISSUE;
D O I
10.1016/j.bjoms.2023.08.240
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
In this study we examine the influence of wool-derived keratin intermediate filament proteins (kIFPs) on human dental pulp-derived stem cells (hDPSCs). kIFPs were diluted (10 mg/mL to 0.001 mg/mL) in cell culture media. Effects on hDPSCs proliferation were measured using Alamar blue assay. Keratin concentrations of 1 mg/mL and 0.1 mg/mL were tested for odontogenic differentiation and mineralisation. Alkaline phosphatase (ALP) quantification (7th, 14th, and 21st days), alizarin red S (AR-S) staining and calcium quantification (21st day), reverse transcription polymerase chain reaction (RT-PCR, collagen expression), and immunocytochemical staining for dentin matrix protein (DMP) were performed. hDPSCs showed higher proliferation with kIFPs of 0.1 mg/mL or less (p < 0.0001). The 0.1 mg/mL keratin concentration promoted odontogenic differentiation, confirmed by increased ALP activity, significant calcium deposits (AR-S staining, p < 0.05), upregulated collagen expression (RT-PCR, p < 0.05), and positive DMP staining. These results suggest that kIFPs could be a potential biomaterial for pulp-dentin regeneration.(c) 2023 The British Association of Oral and Maxillofacial Surgeons. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:617 / 622
页数:6
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