双功能肽DPI-VTK促进间充质干细胞迁移促进骨再生

IF 3.9 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Eric J. Madsen, Seungmeen Rhee, Madison Wahlsten, Tia C. Calabrese, David H. Kohn
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引用次数: 0

摘要

在不使用外源细胞的情况下,利用趋化因子和粘附因子靶向特定宿主细胞群是一种很有前途的诱导骨再生策略。从噬菌体展示中获得了两个肽序列:间充质干细胞(MSC)结合DPI (DPIYALSWSGMA)序列和磷灰石结合VTK (VTKHLNQISQSY)序列。当DPI-VTK组合成双功能序列时,DPI-VTK增加了间充质干细胞与磷灰石表面的粘附强度和移植间充质干细胞成骨的数量。由于许多粘附分子可以刺激趋化性,并且细胞对肽DPI-VTK的粘附是由整合素介导的,这对迁移也至关重要,因此我们假设DPI-VTK是一种msc特异性趋化因子,可以通过促进迁移宿主MSCs的体内成骨来增加骨再生。在transwell实验中,当DPI-VTK用作化学引诱剂时,诱导多能干细胞衍生的人间充质干细胞(p < 0.0001)和小鼠原代颅骨细胞(p < 0.0001)在体外的迁移能力显著增加。利用流式细胞术进一步表征小鼠颅骨DPI-VTK结合细胞,发现对表达MSC标志物(CD29、CD73、CD90、CD105、CD106、Sca-1、CD44和CD200)的细胞具有特异性。在体内与矿化支架结合后,DPI-VTK增加了CD90和CD200阳性细胞的迁移(p < 0.05),与无肽对照相比,DPI-VTK增加了骨形成(p < 0.05)。这些结果证明了噬菌体展示在创造多功能肽方面的效用,这些多肽可以增加体内的迁移、粘附和骨形成,这种策略可以应用于许多不同的细胞类型和系统。研究结果从两个方面促进了基于生物材料的骨再生——证明了噬菌体衍生肽能够增加MSCs在体内的迁移和增加宿主介导的骨再生——可能绕过细胞移植。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dual-Functional Peptide DPI-VTK Promotes Mesenchymal Stem Cell Migration for Bone Regeneration

Dual-Functional Peptide DPI-VTK Promotes Mesenchymal Stem Cell Migration for Bone Regeneration

Targeting specific populations of host cells with chemotactic and adhesion factors is a promising strategy for inducing bone regeneration without the use of exogenous cells. Two peptide sequences have been derived from phage display: the mesenchymal stem cell (MSC) binding DPI (DPIYALSWSGMA) sequence and the apatite binding VTK (VTKHLNQISQSY) sequence. When combined into the dual-functional sequence, DPI-VTK increases the adhesion strength of MSCs to apatite surfaces and the amount of bone formation with transplanted MSCs. Because many adhesion molecules can stimulate chemotaxis, and cell adhesion to peptide DPI-VTK is mediated by integrins also critical to migration, we hypothesized that DPI-VTK serves as an MSC-specific chemotactic factor and can increase bone regeneration by promoting the osteogenesis of the migrated host MSCs in vivo. In transwell assays, induced pluripotent stem cell-derived human MSCs (p < 0.0001) and primary mouse calvarial cells (p < 0.0001) showed significantly increased migration in vitro when DPI-VTK was used as a chemoattractant. Further characterization of DPI-VTK binding cells from mouse calvaria using flow cytometry showed specificity toward cells expressing MSC markers (CD29, CD73, CD90, CD105, CD106, Sca-1, CD44, and CD200). When conjugated to a mineralized scaffold in vivo, DPI-VTK increased the migration of CD90 and CD200 positive cells (p < 0.05) and increased bone formation versus no-peptide controls (p < 0.05). These results demonstrate the utility of phage display in creating multifunctional peptides that can increase migration, adhesion, and bone formation in vivo, a strategy that could be applied to numerous different cell types and systems. Results advance biomaterials-based bone regeneration in two ways—demonstrating the ability of the phage-derived peptides to increase the migration of MSCs in vivo and increase host-mediated bone regeneration—potentially bypassing cell transplantation.

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来源期刊
Journal of biomedical materials research. Part A
Journal of biomedical materials research. Part A 工程技术-材料科学:生物材料
CiteScore
10.40
自引率
2.00%
发文量
135
审稿时长
3.6 months
期刊介绍: The Journal of Biomedical Materials Research Part A is an international, interdisciplinary, English-language publication of original contributions concerning studies of the preparation, performance, and evaluation of biomaterials; the chemical, physical, toxicological, and mechanical behavior of materials in physiological environments; and the response of blood and tissues to biomaterials. The Journal publishes peer-reviewed articles on all relevant biomaterial topics including the science and technology of alloys,polymers, ceramics, and reprocessed animal and human tissues in surgery,dentistry, artificial organs, and other medical devices. The Journal also publishes articles in interdisciplinary areas such as tissue engineering and controlled release technology where biomaterials play a significant role in the performance of the medical device. The Journal of Biomedical Materials Research is the official journal of the Society for Biomaterials (USA), the Japanese Society for Biomaterials, the Australasian Society for Biomaterials, and the Korean Society for Biomaterials. Articles are welcomed from all scientists. Membership in the Society for Biomaterials is not a prerequisite for submission.
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