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Conference Paper: Peptide Hydrogel Scaffold Promotes Angiogenesis And Osteo/Odontogenic Differentiation In-Vitro
Title | Peptide Hydrogel Scaffold Promotes Angiogenesis And Osteo/Odontogenic Differentiation In-Vitro |
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Authors | |
Keywords | Biomaterials Pulp Regeneration Stem Cells and Tissue engineering |
Issue Date | 2013 |
Publisher | Sage Publications, Inc. The Journal's web site is located at http://www.sagepub.com/journalsProdDesc.nav?prodId=Journal201925 |
Citation | The 91st General Session & Exhibition of the International Association for Dental Research (IADR), Seattle, Washington, USA, 20-23 March 2013. In Journal of Dental Research, 2013, v. 92 n. Special Issue A: abstract no. 3605 How to Cite? |
Abstract | Objectives: To investigate cell viability, vascular network formation and differentiation of mono- or co-cultured human dental pulp stem cells (DPSCs) and human umbilical vein endothelial cells (HUVECs) within a three-dimensional peptide hydrogel scaffold (PHS).
Methods: Monocultures and combinations of co-cultures (3:1, 1:1, 1:3) of DPSCs and HUVECs were encapsulated in different concentrations (0.5%, 0.25%, 0.15%) of PHS (BD-Biosciences, Bedford, MA). DPSCs and HUVECs were transfected with green fluorescent protein and red fluorescent protein respectively using pre-made lentiviral particles (GenTarget Inc, San Diego, CA) before encapsulation. Cellular morphologies and 3-dimensional organization of cultures within PHS were monitored using confocal microscopy. Cell viability was assessed using a live/dead viability assay kit at day 7 and 14. Cell cultures within PHS were induced for odonto/osteogenic differentiation (up to 21-days), examined for alkaline phosphatase (ALP) activity (ALP quantification assay) and mineralization (Von-Kossa staining). Experiments were conducted in triplicate using DPSCs from three different donors and statistically analysed (ANOVA).
Results: Live/dead assay revealed 0.15% as the optimum PHS concentration with a significantly high survival of HUVECs compared to 0.5% and 0.25% PHS. In monocultures, DPSCs survived and grew faster than HUVECs. In co-cultures both cells survived well and HUVECs formed an extensive vessel-like network throughout the PHS compared to HUVEC monocultures where it failed to form any vessel-like structures. This finding suggested that co-culture inhibits HUVECs apoptosis and secretes angiogenic factors to promote vessel-like network formation. At higher endothelial cell counts, the density of vessel-like structures was low and DPSC:HUVEC 3:1 was found as the optimum ratio. ALP activity of cells in co-culture was higher than that of DPSCs in monocultures (p<0.05). Despite the ratio, all the co-cultures showed higher amount of mineralization compared to monocultures.
Conclusion: These findings indicate that PHS promotes angiogenesis and osteo/odontogenic differentiation and has potential for engineering vascularised-pulp tissues. |
Description | Poster Presentation Session 406: Oral Tissues |
Persistent Identifier | http://hdl.handle.net/10722/183221 |
ISSN | 2023 Impact Factor: 5.7 2023 SCImago Journal Rankings: 1.909 |
DC Field | Value | Language |
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dc.contributor.author | Dissanayaka, WL | en_US |
dc.contributor.author | Zhang, C | en_US |
dc.contributor.author | Hargreaves, K | en_US |
dc.contributor.author | Jin, L | en_US |
dc.date.accessioned | 2013-05-15T01:48:19Z | - |
dc.date.available | 2013-05-15T01:48:19Z | - |
dc.date.issued | 2013 | en_US |
dc.identifier.citation | The 91st General Session & Exhibition of the International Association for Dental Research (IADR), Seattle, Washington, USA, 20-23 March 2013. In Journal of Dental Research, 2013, v. 92 n. Special Issue A: abstract no. 3605 | en_US |
dc.identifier.issn | 0022-0345 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/183221 | - |
dc.description | Poster Presentation | - |
dc.description | Session 406: Oral Tissues | - |
dc.description.abstract | Objectives: To investigate cell viability, vascular network formation and differentiation of mono- or co-cultured human dental pulp stem cells (DPSCs) and human umbilical vein endothelial cells (HUVECs) within a three-dimensional peptide hydrogel scaffold (PHS). Methods: Monocultures and combinations of co-cultures (3:1, 1:1, 1:3) of DPSCs and HUVECs were encapsulated in different concentrations (0.5%, 0.25%, 0.15%) of PHS (BD-Biosciences, Bedford, MA). DPSCs and HUVECs were transfected with green fluorescent protein and red fluorescent protein respectively using pre-made lentiviral particles (GenTarget Inc, San Diego, CA) before encapsulation. Cellular morphologies and 3-dimensional organization of cultures within PHS were monitored using confocal microscopy. Cell viability was assessed using a live/dead viability assay kit at day 7 and 14. Cell cultures within PHS were induced for odonto/osteogenic differentiation (up to 21-days), examined for alkaline phosphatase (ALP) activity (ALP quantification assay) and mineralization (Von-Kossa staining). Experiments were conducted in triplicate using DPSCs from three different donors and statistically analysed (ANOVA). Results: Live/dead assay revealed 0.15% as the optimum PHS concentration with a significantly high survival of HUVECs compared to 0.5% and 0.25% PHS. In monocultures, DPSCs survived and grew faster than HUVECs. In co-cultures both cells survived well and HUVECs formed an extensive vessel-like network throughout the PHS compared to HUVEC monocultures where it failed to form any vessel-like structures. This finding suggested that co-culture inhibits HUVECs apoptosis and secretes angiogenic factors to promote vessel-like network formation. At higher endothelial cell counts, the density of vessel-like structures was low and DPSC:HUVEC 3:1 was found as the optimum ratio. ALP activity of cells in co-culture was higher than that of DPSCs in monocultures (p<0.05). Despite the ratio, all the co-cultures showed higher amount of mineralization compared to monocultures. Conclusion: These findings indicate that PHS promotes angiogenesis and osteo/odontogenic differentiation and has potential for engineering vascularised-pulp tissues. | - |
dc.language | eng | en_US |
dc.publisher | Sage Publications, Inc. The Journal's web site is located at http://www.sagepub.com/journalsProdDesc.nav?prodId=Journal201925 | en_US |
dc.relation.ispartof | Journal of Dental Research | en_US |
dc.rights | Journal of Dental Research. Copyright © Sage Publications, Inc. | en_US |
dc.subject | Biomaterials | - |
dc.subject | Pulp | - |
dc.subject | Regeneration | - |
dc.subject | Stem Cells and Tissue engineering | - |
dc.title | Peptide Hydrogel Scaffold Promotes Angiogenesis And Osteo/Odontogenic Differentiation In-Vitro | en_US |
dc.type | Conference_Paper | en_US |
dc.identifier.email | Zhang, C: zhangcf@hku.hk | en_US |
dc.identifier.email | Jin, L: ljjin@hkucc.hku.hk | en_US |
dc.identifier.authority | Zhang, C=rp01408 | en_US |
dc.identifier.authority | Jin, L=rp00028 | en_US |
dc.identifier.hkuros | 214400 | en_US |
dc.identifier.volume | 92 | en_US |
dc.identifier.issue | Special Issue A: abstract no. 3605 | en_US |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0022-0345 | - |