4.7 Article

Mimicking Bone Extracellular Matrix: From BMP-2-Derived Sequences to Osteogenic-Multifunctional Coatings

期刊

ADVANCED HEALTHCARE MATERIALS
卷 11, 期 20, 页码 -

出版社

WILEY
DOI: 10.1002/adhm.202201339

关键词

biomimetic peptides; cell adhesions; multifunctionality; osteogenic differentiation; RGD-DWIVA; titanium biofunctionalization

资金

  1. Spanish State Research Agency [RYC-2015-18566, MAT2017-83905-R, PID2020-114019RB-I00/AEI/10.13039/501100011033]
  2. AGAUR [2017 SGR1165]
  3. Generalitat de Catalunya
  4. Max Planck Society
  5. Max Planck School Matter to Life (German Federal Ministry of Education and Research, BMBF)
  6. National Research Foundation of Korea (NRF) - Priority Research Center Program
  7. Ministry of Education [2019R1A6A1A11034536]
  8. Global Research Development Center Program [2018K1A4A3A01064257]
  9. Medical Research Center Program [2021R1A5A2022318]
  10. European Union [872869]
  11. AGAUR (FI-2018 predoctoral fellowship)
  12. Marie Curie Actions (MSCA) [872869] Funding Source: Marie Curie Actions (MSCA)

向作者/读者索取更多资源

Cell-material interactions can be regulated by mimicking bone extracellular matrix on the surface of biomaterials. Synthetic osteogenic domains derived from BMP-2 are gaining attention as a strategy for bone regeneration without clinical risks associated with the molecule. Screening of the BMP-2 epitopes identified peptides that enhance cell adhesion and osteogenic differentiation. The peptides were used to functionalize titanium surfaces, showing improved bone formation and reduced fibrous tissue thickness.
Cell-material interactions are regulated by mimicking bone extracellular matrix on the surface of biomaterials. In this regard, reproducing the extracellular conditions that promote integrin and growth factor (GF) signaling is a major goal to trigger bone regeneration. Thus, the use of synthetic osteogenic domains derived from bone morphogenetic protein 2 (BMP-2) is gaining increasing attention, as this strategy is devoid of the clinical risks associated with this molecule. In this work, the wrist and knuckle epitopes of BMP-2 are screened to identify peptides with potential osteogenic properties. The most active sequences (the DWIVA motif and its cyclic version) are combined with the cell adhesive RGD peptide (linear and cyclic variants), to produce tailor-made biomimetic peptides presenting the bioactive cues in a chemically and geometrically defined manner. Such multifunctional peptides are next used to functionalize titanium surfaces. Biological characterization with mesenchymal stem cells demonstrates the ability of the biointerfaces to synergistically enhance cell adhesion and osteogenic differentiation. Furthermore, in vivo studies in rat calvarial defects prove the capacity of the biomimetic coatings to improve new bone formation and reduce fibrous tissue thickness. These results highlight the potential of mimicking integrin-GF signaling with synthetic peptides, without the need for exogenous GFs.

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