PHBV/bioglass composite scaffolds with co-cultures of endothelial cells and bone marrow stromal cells improve vascularization and osteogenesis for bone tissue engineering. Issue 36 (21st April 2017)
- Record Type:
- Journal Article
- Title:
- PHBV/bioglass composite scaffolds with co-cultures of endothelial cells and bone marrow stromal cells improve vascularization and osteogenesis for bone tissue engineering. Issue 36 (21st April 2017)
- Main Title:
- PHBV/bioglass composite scaffolds with co-cultures of endothelial cells and bone marrow stromal cells improve vascularization and osteogenesis for bone tissue engineering
- Authors:
- Wu, Jun
Wu, Zhi
Xue, Zhenqiang
Li, Haiyan
Liu, Jinbo - Abstract:
- Abstract : PHBV + 10% BG composite scaffolds stimulated osteogenic differentiation and angiogenic differentiation of co-cultures of HBMSCs and HUVECs by enhancing paracrine effects between the two types of cells. Abstract : Polyhydroxybutyrate–polyhydroxyvalerate (PHBV) and bioglass (BG) have been widely reported to be suitable for bone tissue engineering. However, composite scaffolds with polymers and bioceramics have shown advantages over pure polymer and bioceramic scaffolds for bone tissue engineering. In addition, recent studies have shown that cross-talk between endothelial cells and osteoblastic cells can stimulate bone regeneration compared to tissue engineering constructs containing only one type of cell. Therefore, in this study, we aim to construct an improved engineered bone containing PHBV/BG composite scaffold with co-cultures of human umbilical vein endothelial cells (HUVECs) and human bone marrow stromal cells (HBMSCs) in order to enhance osteogenesis and angiogenesis of bone repair. Results showed that addition of BG into PHBV could enhance osteogenic differentiation of co-cultured HBMSCs and vascularization of co-cultured HUVECs by upregulating paracrine effects between the two types of cells compared to pure PHBV scaffolds. Among all groups, composite scaffolds containing PHBV with 10% BG showed the strongest stimulatory effects on osteogenic differentiation and vascularization due to their appropriate ion products, specifically, the appropriateAbstract : PHBV + 10% BG composite scaffolds stimulated osteogenic differentiation and angiogenic differentiation of co-cultures of HBMSCs and HUVECs by enhancing paracrine effects between the two types of cells. Abstract : Polyhydroxybutyrate–polyhydroxyvalerate (PHBV) and bioglass (BG) have been widely reported to be suitable for bone tissue engineering. However, composite scaffolds with polymers and bioceramics have shown advantages over pure polymer and bioceramic scaffolds for bone tissue engineering. In addition, recent studies have shown that cross-talk between endothelial cells and osteoblastic cells can stimulate bone regeneration compared to tissue engineering constructs containing only one type of cell. Therefore, in this study, we aim to construct an improved engineered bone containing PHBV/BG composite scaffold with co-cultures of human umbilical vein endothelial cells (HUVECs) and human bone marrow stromal cells (HBMSCs) in order to enhance osteogenesis and angiogenesis of bone repair. Results showed that addition of BG into PHBV could enhance osteogenic differentiation of co-cultured HBMSCs and vascularization of co-cultured HUVECs by upregulating paracrine effects between the two types of cells compared to pure PHBV scaffolds. Among all groups, composite scaffolds containing PHBV with 10% BG showed the strongest stimulatory effects on osteogenic differentiation and vascularization due to their appropriate ion products, specifically, the appropriate concentration of silicon ions. In vivo results also demonstrated that PHBV containing 10% BG scaffolds with co-cultures of HUVECs and HBMSCs showed the strongest stimulatory effects on osteogenesis and angiogenesis among all groups. Taken together, PHBV/BG scaffolds with co-cultures of endothelial cells and osteogenic cells possess great application potential for bone tissue engineering. … (more)
- Is Part Of:
- RSC advances. Volume 7:Issue 36(2017)
- Journal:
- RSC advances
- Issue:
- Volume 7:Issue 36(2017)
- Issue Display:
- Volume 7, Issue 36 (2017)
- Year:
- 2017
- Volume:
- 7
- Issue:
- 36
- Issue Sort Value:
- 2017-0007-0036-0000
- Page Start:
- 22197
- Page End:
- 22207
- Publication Date:
- 2017-04-21
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7ra02767b ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 370.xml