Directed osteogenic differentiation of human bone marrow mesenchymal stem cells via sustained release of BMP4 from PBVHx-based nanoparticles

被引:13
作者
Huang, Xiao-Yun [1 ,5 ]
Zhou, Xiao-Xiang [1 ]
Yang, Hui [1 ]
Xu, Tao [1 ]
Dao, Jin-Wei [3 ]
Bian, Li [5 ]
Wei, Daixu [1 ,2 ,3 ,4 ]
机构
[1] Qujing Med Coll, Sch Clin Med, Qujing 655000, Peoples R China
[2] Chengdu Univ, Sch Clin Med, Chengdu, Peoples R China
[3] Southwest Med Univ, Zigong Inst Brain Sci, Zigong Psychiat Res Ctr, Zigong Affiliated Hosp, Zigong 643002, Peoples R China
[4] Northwest Univ, Sch Med, Dept Life Sci & Med, Key Lab Resource Biol & Biotechnol Western China,M, Xian 710069, Peoples R China
[5] Kunming Med Univ, Affiliated Hosp 1, Dept Pathol, Kunming 650032, Peoples R China
关键词
BMP4; Nanoparticles; Polyhydroxyalkanoates; MORPHOGENETIC PROTEIN-2; GENE-EXPRESSION; SCAFFOLDS; TISSUE; DELIVERY; REGENERATION; ENHANCEMENT; CARTILAGE; REPAIR;
D O I
10.1016/j.ijbiomac.2024.130649
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 Morphogenetic Protein 4 (BMP4) is crucial for bone and cartilage tissue regeneration, essential in medical tissue engineering, cosmetology, and aerospace. However, its cost and degradation susceptibility pose significant clinical challenges. To enhance its osteogenic activity while reducing dosage and administration frequency, we developed a novel long -acting BMP4 delivery system using poly(3-hydroxybutyrate- co -3-hydroxyvalerate-co-3- hydroxyhexanoate) (PBVHx) nanoparticles with soybean lecithin -modified BMP4 (sBP-NPs). These nanoparticles promote directed osteogenic differentiation of human bone marrow mesenchymal stem cells (hBMSCs) through sustained BMP4 release. sBP-NPs exhibited uniform size (100 - 200 nm) and surface charges, with higher BMP4 entrapment efficiency (82.63 %) compared to controls. After an initial burst release within 24 h, sBP-NPs achieved 80 % cumulative BMP4 release within 20 days, maintaining levels better than control BP -NPs with unmodified BMP4. Co -incubation and nanoparticle uptake experiments confirmed excellent biocompatibility of sBP-NPs, promoting hBMSC differentiation towards osteogenic lineage with increased expression of type I collagen, calcium deposition, and ALP activity ( > 20,000 U/g protein) compared to controls. Moreover, hBMSCs treated with sBP-NPs exhibited heightened expression of osteogenic genetic markers, surpassing control groups. Hence, this innovative strategy of sustained BMP4 release from sBP-NPs holds potential to revolutionize bone regeneration in minimally invasive surgery, medical cosmetology or space environments.
引用
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页数:10
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