PLLA scaffolds produced by thermally induced phase separation (TIPS) allow human chondrocyte growth and extracellular matrix formation dependent on pore size

被引:80
作者
Conoscenti, Gioacchino [1 ]
Schneider, Tobias [2 ,3 ]
Stoelzel, Katharina [4 ]
Pavia, Francesco Carfi [1 ]
Brucato, Valerio [1 ]
Goegele, Clemens [2 ]
La Carrubba, Vincenzo [1 ]
Schulze-Tanzil, Gundula [2 ]
机构
[1] Univ Palermo, Bio & Tissue Engn Lab, Dept Civil, Environm,Aerosp,Mat Engn, Palermo, Italy
[2] Paracelsus Med Univ, Inst Anat, Prof Ernst Nathan Str 1, D-90419 Salzburg Nuremberg, Nuremberg, Germany
[3] Charite, Dept Orthopaed Trauma & Reconstruct Surg, Campus Benjamin Franklin, Berlin, Germany
[4] Charite, Campus Charite Mitte, Dept Otorhinolaryngol Head & Neck Surg, Berlin, Germany
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2017年 / 80卷
关键词
Cartilage; Tissue engineering; Poly(L)lactic acid; Articular chondrocytes; Nasoseptal chondrocytes; Type II collagen; L-LACTIC ACID; MESENCHYMAL STROMAL CELLS; ADIPOSE STEM-CELLS; CHONDROGENIC DIFFERENTIATION; ARTICULAR CHONDROCYTES; MECHANICAL-PROPERTIES; CARTILAGE; MORPHOLOGY; GRADIENT; FOAMS;
D O I
10.1016/j.msec.2017.06.011
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Damage of hyaline cartilage species such as nasoseptal or joint cartilage requires proper reconstruction, which remains challenging due to the low intrinsic repair capacity of this tissue. Implantation of autologous chondrocytes in combination with a biomimetic biomaterial represents a promising,strategy to support cartilage repairThe aim of this work was to assess the viability, attachment, morphology, extracellular matrix (ECM) production of human articular and nasoseptal chondrocytes cultured in vitro in porous poly(L-lactic) (PLLA) scaffolds of two selected pore sizes (100 and 200 mu m). The PLLA scaffolds with 100 and 200 mu m pore sizes were prepared via ternary thermally induced phase separation (TIPS) technique and analyzed using scanning electron microscopy (SEM). Articular and nasoseptal chondrocytes were seeded on the scaffold and cultures maintained for 7 and 14 days. Live/dead staining, (immuno-)histology and gene expression analysis of type II, type I collagen, aggrecan and SOX9 were performed to assess scaffold cytocompatibility and chondrocyte phenotypE. The majority of both chondrocyte types survived on both scaffolds for the whole culture period. Hematoxylin-eosin (HE), alcian blue (visualizing glycosaminoglycans) stainings, immunoreactivity and gene expression of ECM proteins and cartilage marker (type II, I collagen, aggrecan, SOX9) of the chondrocyte scaffold constructs indicated that the smaller pore dimensions promoted the differentiation of the chondrocytes compared with the larger pore size. The present work revealed that the scaffold pore size is an important factor influencing chondrocyte differentiation and indicated that the scaffolds with 100 mu m pores serve as a cytocompatible basis for further future modifications. (C) 2017 Published by Elsevier B.V.
引用
收藏
页码:449 / 459
页数:11
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