Enhancement of Osteogenic Induction by LL37 Modified with a Collagen-Binding Domain In Vitro and In Vivo

被引:0
|
作者
Lin, Xiaoxuan [1 ]
Chen, Sipeng [1 ]
Quan, Jingjing [1 ]
Zhang, Qi [1 ]
Liao, Muzi [1 ]
Ma, Xinyue [1 ]
Zheng, Yuyan [2 ]
Mai, Sui [1 ]
机构
[1] Sun Yat Sen Univ, Guanghua Sch Stomatol, Hosp Stomatol, Guangdong Prov Key Lab Stomatol, Guangzhou, Peoples R China
[2] Southern Univ Sci & Technol, Jinan Univ, Affiliated Hosp 1, Dept Stomatol,Shenzhen Peoples Hosp,Sch Clin Med, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
LL37; Collagen-binding domain; Osteoinduction;
D O I
10.1007/s10989-021-10216-w
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
Bone defect diseases, particularly those induced by inflammation, pose a challenge for the design of ideal drug-loading scaffolds that could facilitate bone repair and eliminate inflammatory pathogens. Antimicrobial peptides LL37 is considered a promising alternative loading drug due to its broad-spectrum antimicrobial effect and various bio-functions, including osteogenic induction. In this study, we synthesized modified LL37 by adding a collagen-binding domain (CBD) to achieve specific binding to collagen and a slow release pattern. The modified peptide was indicated to exhibit similar biological activities as natural LL37 on rat BMSCs, including promotion of migration activity, anti-inflammatory activity and osteogenic induction in vitro. Ectopic bone formation experiments further confirmed the angiogenesis and osteoinduction activities in vivo. Collectively, the results indicate that LL37-CBD may be a potential loading drug for preventative and curative applications in the treatment of inflammation-induced bone diseases.
引用
收藏
页码:1861 / 1873
页数:13
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