Versatile effects of magnesium hydroxide nanoparticles in PLGA scaffold-mediated chondrogenesis

Authors
Park, Kwang-SookKim, Byoung-JuLih, EugenePark, WooramLee, Soo-HongJoung, Yoon KiHan, Dong Keun
Issue Date
2018-06
Publisher
ELSEVIER SCI LTD
Citation
ACTA BIOMATERIALIA, v.73, pp.204 - 216
Abstract
Artificial scaffolds made up of various synthetic biodegradable polymers have been reported to have many advantages including cheap manufacturing, easy scale up, high mechanical strength, convenient manipulation, and molding into an unlimited variety of shapes. However, the synthetic biodegradable polymers still have the insufficiency for cartilage regeneration owing to their acidic degradation products. To reduce acidification by degradation of synthetic polymers, we incorporated magnesium hydroxide (MH) nanoparticles into porous polymer scaffold not only to effectively neutralize the acidic hydrolysate but also to minimize the structural disturbance of scaffolds. The neutralization effect of poly(D,L-lactic-co-glycolic acid; PLGA)/MH scaffold was confirmed with the maintenance of neutral pH, contrary to a PLGA scaffold with low pH. Further, the scaffolds were applied to evaluate the chondrogenic differentiation of the human bone marrow mesenchymal stem cells. In in vitro study, the PLGA/MH scaffold enhanced the chondrogenesis markers and reduced the calcification, compared to the PLGA scaffold. Additionally, the PLGA/MH scaffold reduced the release of inflammatory cytokines, compared to the PLGA scaffold, as the cell death decreased. Moreover, the addition of MH reduced necrotic cell death at the early stage of chondrogenic differentiation. Further, the necrotic cell death by the PLGA scaffold was mediated by cleavage of caspase-1, the so-called interleukin 1-converting enzyme, and MH alleviated it as well as nuclear factor kappa B expression. Furthermore, the PLGA/MH scaffold highly supported chondrogenic healing of rat osteochondral defect sites in in vivo study. Therefore, it was suggested that a synthetic polymer scaffold containing MH could be a novel healing tool to support cartilage regeneration and further treatment of orthopedic patients. (C) 2018 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
Keywords
MESENCHYMAL STEM-CELLS; ARTICULAR CHONDROCYTES; EXTRACELLULAR PH; MATRIX SYNTHESIS; TNF-ALPHA; CARTILAGE; CALCIFICATION; STABILITY; ACID; DIFFERENTIATION; MESENCHYMAL STEM-CELLS; ARTICULAR CHONDROCYTES; EXTRACELLULAR PH; MATRIX SYNTHESIS; TNF-ALPHA; CARTILAGE; CALCIFICATION; STABILITY; ACID; DIFFERENTIATION; Magnesium hydroxide; Chondrogenesis; Calcification; Cell death; Inflammation
ISSN
1742-7061
URI
https://pubs.kist.re.kr/handle/201004/121300
DOI
10.1016/j.actbio.2018.04.022
Appears in Collections:
KIST Article > 2018
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