A Nanostructured Synthetic Collagen Mimic for Hemostasis

被引:136
作者
Kumar, Vivek A. [1 ]
Taylor, Nichole L. [1 ]
Jalan, Abhishek A. [1 ]
Hwang, Lyahn K. [1 ]
Wang, Benjamin K. [1 ]
Hartgerink, Jeffery D. [1 ]
机构
[1] Rice Univ, Dept Bioengn, Dept Chem, Houston, TX 77030 USA
基金
美国国家科学基金会;
关键词
GLYCOPROTEIN-VI; TRIPLE-HELIX; IN-VITRO; SELF-ASSOCIATION; STRUCTURAL BASIS; MIMETIC PEPTIDE; SCAFFOLDS; RECEPTOR; IMMUNOGENICITY; NANOPARTICLES;
D O I
10.1021/bm500091e
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Collagen is a major component of the extracellular matrix and plays a wide variety of important roles in blood clotting, healing, and tissue remodeling. Natural, animal derived, collagen is used in many clinical applications but concerns exist with respect to its role in inflammation, batch-to-batch variability, and possible disease transfection. Therefore, development of synthetic nanomaterials that can mimic the nanostructure and properties of natural collagen has been a heavily pursued goal in biomaterials. Previously, we reported on the design and multihierarchial self-assembly of a 36 amino acid collagen mimetic peptide (KOD) that forms nanofibrous triple helices that entangle to form a hydrogel. In this report, we utilize this nanofiber forming collagen mimetic peptide as a synthetic biomimetic matrix useful in thrombosis. We demonstrate that nanofibrous KOD synthetic collagen matrices adhere platelets, activate them (indicated by soluble P-selectin secretion), and clot plasma and blood similar to animal derived collagen and control surfaces. In addition to the thrombotic potential, THP-1 monocytes incubated with our KOD collagen mimetic showed minimal proinflammatory c-ytokine (TNF-alpha or IL-1 beta) production. Together, the data presented demonstrates the potential of a novel synthetic collagen mimetic as a hemostat.
引用
收藏
页码:1484 / 1490
页数:7
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