RESUMO
The carbon fiber/hydroxyapatite (CF/HA) reinforcement with a three-dimensional flower-like structure was rapidly fabricated with the biomimetic mineralization method to strengthen the interfacial performance and bioactivity of carbon fiber/polyether ether ketone (CF/PEEK) composites. Silk fibroin (SF), which can construct a robust interphase between CF and PEEK, supported an organic template to regulate the growth of inorganic HA. The interfacial properties were markedly enhanced through mechanical interlocking and interface adhesion induced by increasing roughness and surface energy of CF. Besides, the mineralization time was significantly reduced after the addition of cetyltrimethylammonium bromide to the simulated body fluid, and the prepared CF/HA possessed good bioactivity. In this study, the interlaminar shear strength (ILSS) and flexural strength of CF-HA/45/PEEK composites demonstrated an enhancement of 45.9% and 51.2%, respectively, compared to the untreated CF/PEEK composites. It is predicted that this strategy could provide a rapid and convenient route to ameliorate the interfacial performance and bioactivity of CF/PEEK composites simultaneously.
Assuntos
Materiais Biocompatíveis , Durapatita , Durapatita/farmacologia , Durapatita/química , Fibra de Carbono , Biomineralização , Polietilenoglicóis/química , CetonasRESUMO
CXCL-12 and its receptor CXCR4 participate in breast cancer and melanoma cell metastasis to bone and lymphoid nodes. CD44, as a receptor for hyaluronic acid, is involved in lymphocyte recirculation, homing, adhesion and migration. But the role of CD44 in CXCL-12 induced leukemia cell migration still remains unclear. The present study showed that CXCL-12 stimulation induced the rapid internalization of CXCR4 and facilitated the formation of lamellipodia and uropod in acute leukemia cell line HL-60. CXCL-12 also induced CD44 translocation into the uropod, while CD44 remained evenly distributed on the untreated cell membranes. Results suggest that CD44 participates in CXCL-12 induced cell polarization and subsequent cell migration.
Assuntos
Polaridade Celular , Quimiocina CXCL12/imunologia , Receptores de Hialuronatos/imunologia , Leucemia Mieloide Aguda/imunologia , Animais , Movimento Celular/fisiologia , Extensões da Superfície Celular/metabolismo , Células HL-60 , Humanos , Receptores CXCR4RESUMO
CXCL-12 and its receptor CXCR4 participate in breast cancer and melanoma cell metastasis to bone and lymphoid nodes. CD44, as a receptor for hyaluronic acid, is involved in lymphocyte recirculation, homing, adhesion and migration. But the role of CD44 in CXCL-12 induced leukemia cell migration still remains unclear. The present study showed that CXCL-12 stimulation induced the rapid internalization of CXCR4 and facilitated the formation of lamellipodia and uropod in acute leukemia cell line HL-60. CXCL-12 also induced CD44 translocation into the uropod, while CD44 remained evenly distributed on the untreated cell membranes. Results suggest that CD44 participates in CXCL-12 induced cell polarization and subsequent cell migration.
Assuntos
Humanos , /imunologia , Extensões da Superfície Celular/metabolismo , Leucemia Mieloide/imunologia , Movimento Celular/fisiologia , Polaridade Celular , Ácido Hialurônico , Quimiocinas/imunologiaRESUMO
CXCL-12 and its receptor CXCR4 participate in breast cancer and melanoma cell metastasis to bone and lymphoid nodes. CD44, as a receptor for hyaluronic acid, is involved in lymphocyte recirculation, homing, adhesion and migration. But the role of CD44 in CXCL-12 induced leukemia cell migration still remains unclear. The present study showed that CXCL-12 stimulation induced the rapid internalization of CXCR4 and facilitated the formation of lamellipodia and uropod in acute leukemia cell line HL-60. CXCL-12 also induced CD44 translocation into the uropod, while CD44 remained evenly distributed on the untreated cell membranes. Results suggest that CD44 participates in CXCL-12 induced cell polarization and subsequent cell migration.(AU)
