组织蛋白酶K
破骨细胞
化学
兰克尔
酸性磷酸酶
抗酒石酸酸性磷酸酶
组织蛋白酶
细胞生物学
壳聚糖
降钙素受体
分子生物学
生物物理学
体外
受体
生物化学
激活剂(遗传学)
生物
酶
降钙素基因相关肽
神经肽
作者
Christiane Heinemann,Sascha Heinemann,Anne Bernhardt,Anja Lode,H. Worch,Thomas Hanke
摘要
Textile chitosan fibre scaffolds were evaluated in terms of interaction with osteoclast-like cells, derived from human primary monocytes.Part of the scaffolds was further modified by coating with fibrillar collagen type I in order to make the surface biocompatible.Monocytes were cultured directly on the scaffolds in the presence of macrophage colony stimulating factor (M-CSF) and receptor activator of nuclear factor kappaB ligand (RANKL) for up to 18 days.Confocal laser scanning microscopy (CLSM) as well as scanning electron microscopy (SEM) revealed the formation of multinuclear osteoclast-like cells on both the raw chitosan fibres and the collagen-coated scaffolds.The modified surface supported the osteoclastogenesis.Differentiation towards the osteoclastic lineage was confirmed by the microscopic detection of cathepsin K, tartrate resistant acid phosphatase (TRAP), acidic compartments using 3-(2,4-dinitroanillino)-3'-amino-N-methyldipropylamine (DAMP), immunological detection of TRAP isoform 5b, and analysis of gene expression of the osteoclastic markers TRAP, cathepsin K, vitronectin receptor, and calcitonin receptor using reverse transcription-polymerase chain reaction (RT-PCR).The feature of the collagen-coated but also of the raw chitosan fibre scaffolds to support attachment and differentiation of human monocytes facilitates cell-induced material resorption -one main requirement for successful bone tissue engineering.
科研通智能强力驱动
Strongly Powered by AbleSci AI