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A multifunctional bioactive material that stimulates osteogenesis and promotes the vascularization bone marrow stem cells and their resistance to bacterial infection.
Ma, Chuang; Wei, Qin; Cao, Bo; Cheng, Xinchun; Tian, Juling; Pu, Hongwei; Yusufu, Aihemaitijiang; Cao, Li.
Afiliação
  • Ma C; Department of Orthopedics Center, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
  • Wei Q; Department of Orthopedics Center, First Affiliated Hospital of Xinjiang Medical University Chang Ji Branch, Chang Ji, China.
  • Cao B; Xinjiang Key Laboratory of Medical Animal Model Research, Clinical Medical Research Institute of the First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
  • Cheng X; Department of Orthopedics Center, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
  • Tian J; Carders Health Care No. 4 Department of Xinjiang Uygur Autonomous Region People's Hospital, Urumqi, China.
  • Pu H; Department of Clinical Laboratory, The first people's Hospital of Urumqi, Urumqi, China.
  • Yusufu A; Department of Science and Research Education Center, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
  • Cao L; Department of Orthopedics Center, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
PLoS One ; 12(3): e0172499, 2017.
Article em En | MEDLINE | ID: mdl-28358890
ABSTRACT
The main limitation of tissue engineering lies in the inability to stimulate osteogenesis, angiogenesis of stem cells and broad-spectrum antimicrobial activity. However, the development of multifunctional bioactive materials with these capabilities remains a great challenge. In this study, we prepared mesoporous silica nanoparticles encapsulated with silver nanocrystals (AG-MSN) with uniform sphere size and mesopores. Platelet-derived growth factor BB (PDGF-BB) was effectively loaded in the AG-MSN mesopores (P-AG-MSN). The silicon ions (Si) released by P-AG-MSN stimulate osteogenic differentiation of bone marrow stromal cells (BMSC) by activating the alkaline phosphatase (ALP) activity of bone-related genes and increasing protein (OCN, RUNX2 and OPN) expression. Ag+ ions could be slowly released from the interior of the shell, highlighting their durable antibacterial activity. The sustained release of PDGF-BB from P-AG-MSN stimulated the angiogenic differentiation of BMSC, as indicated by the enhanced secretion of vascular endothelial growth factor (VEGF), HIF-1α, HGF and ANG-1 and protein expression. Our results show that P-AG-MSN can clearly promote BMSC osteostimulation and vascularization. This research serves as a preliminary study of the utilization of this multifunctional mixture to fabricate a new active biological scaffold that integrates BMSC osteostimulation, vascularization and bactericidal effects by 3D printing technology.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteogênese / Células-Tronco / Infecções Bacterianas / Células-Tronco Hematopoéticas / Proteínas Proto-Oncogênicas c-sis Limite: Humans Idioma: En Revista: PLoS One Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteogênese / Células-Tronco / Infecções Bacterianas / Células-Tronco Hematopoéticas / Proteínas Proto-Oncogênicas c-sis Limite: Humans Idioma: En Revista: PLoS One Ano de publicação: 2017 Tipo de documento: Article