4.7 Article

Ca ions chelation, collagen I incorporation and 3D bionic PLGA/PCL electrospun architecture to enhance osteogenic differentiation

期刊

MATERIALS & DESIGN
卷 198, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.matdes.2020.109300

关键词

Osteogenesis; Ca ions; Collagen I; Bone regeneration; Electrospinning scaffolds

资金

  1. National Natural Science Foundation of China [81801025, 31800843, 61821002, 51832001]
  2. State Key Program of National Natural Science Foundation of China [2017YFA0104302]
  3. Suzhou Science and Technology Development Project [SS2019062]
  4. National Tutor System Training Program for Young Talents in Suzhou Health System

向作者/读者索取更多资源

This study aimed to enhance the osteogenic potential of bioactive synthetic scaffolds through the development of a novel PP/COL I-pDA-Ca scaffold, which showed increased cell adhesion and osteogenic differentiation in cell culture experiments. The incorporation of polydopamine-based Ca chelation, COL I, and 3D bionic structure in the scaffold promoted osteogenesis and cell adhesion, making it an attractive alternative for guided bone regeneration.
Bioactive synthetic scaffolds with 3D porous structure are the most attractive materials among various guided bone regeneration membranes. However, its osteogenic potential is still insufficient. This study was aimed to develop a Calcium surface-anchored Collagen I-PLGA/PCL scaffolds (PP/COL I-pDA-Ca) with enhanced osteogenicity. PP/COL I-pDA-Ca was electrospun from a collagen I-blended PLGA/PCL matrix and then modified by the chelation of Ca-ions via mussel-inspired polydopamine coating. PLGA/PCL, PLGA/PCL-polydopamine, PLGA/PCL-pDA chelated by Ca-ions were used as controls. Osteogenic effects of the scaffolds were examined using MC3T3-E1 cell culture. PP/COL I-pDA-Ca maintained 3D porous architecture with interconnected pores formed by randomly-oriented filamentous fibers and MC3T3-E1 cells cultured on it for 12 h or 24 h were more stretched and spread than those on the controls. PP/COL I-pDA-Ca significantly upregulated alpha 10, alpha 11 and beta 1 integrin expression after 48 h culture. ALP activity, OCN, OSX, BMP2 and RUNX2 expression of MC3T3-E1 cells cultured on PP/COL I-pDA-Ca scaffolds for 7 and 14 days were substantially enhanced when compared to controls (p < 0.05). The pDA-based Ca chelation, COL I incorporation and 3D bionic structure promoted cell adhesion and osteogenic differentiation of MC3T3-E1 cells. This novel PP/COL I-pDA-Ca scaffolds is an attractive alternative for guided bone regeneration. (C) 2020 Published by Elsevier Ltd.

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