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Directed osteogenic differentiation of human bone marrow mesenchymal stem cells via sustained release of BMP4 from PBVHx-based nanoparticles.
Huang, Xiao-Yun; Zhou, Xiao-Xiang; Yang, Hui; Xu, Tao; Dao, Jin-Wei; Bian, Li; Wei, Dai-Xu.
Affiliation
  • Huang XY; School of Clinical Medicine, Qujing Medical College, Qujing 655000, China; Department of Pathology, The First Affiliated Hospital of Kunming Medical University, Kunming 650032, China.
  • Zhou XX; School of Clinical Medicine, Qujing Medical College, Qujing 655000, China.
  • Yang H; School of Clinical Medicine, Qujing Medical College, Qujing 655000, China.
  • Xu T; School of Clinical Medicine, Qujing Medical College, Qujing 655000, China.
  • Dao JW; Zigong Affiliated Hospital of Southwest Medical University, Zigong Psychiatric Research Center, Zigong Institute of Brain Science, Zigong 643002, China.
  • Bian L; Department of Pathology, The First Affiliated Hospital of Kunming Medical University, Kunming 650032, China.
  • Wei DX; School of Clinical Medicine, Qujing Medical College, Qujing 655000, China; School of Clinical Medicine, Chengdu University, Chengdu, China; Zigong Affiliated Hospital of Southwest Medical University, Zigong Psychiatric Research Center, Zigong Institute of Brain Science, Zigong 643002, China; Key Lab
Int J Biol Macromol ; 265(Pt 1): 130649, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38453121
ABSTRACT
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nanoparticles / Mesenchymal Stem Cells Limits: Humans Language: En Journal: Int J Biol Macromol Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nanoparticles / Mesenchymal Stem Cells Limits: Humans Language: En Journal: Int J Biol Macromol Year: 2024 Document type: Article Affiliation country: