File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.biomaterials.2015.10.072
- Scopus: eid_2-s2.0-84949256833
- PMID: 26580785
- Find via

Supplementary
- Citations:
- Appears in Collections:
Article: Hydrogels functionalized with N-cadherin mimetic peptide enhance osteogenesis of hMSCs by emulating the osteogenic niche
| Title | Hydrogels functionalized with N-cadherin mimetic peptide enhance osteogenesis of hMSCs by emulating the osteogenic niche |
|---|---|
| Authors | |
| Keywords | Bio-functionalization of biomaterials Hyaluronic acid hydrogels Mesenchymal stem cells Tissue engineering |
| Issue Date | 2016 |
| Citation | Biomaterials, 2016, v. 77, p. 44-52 How to Cite? |
| Abstract | N-cadherin is considered to be the key factor in directing cell-cell interactions during mesenchymal condensation, which is essential to osteogenesis. In this study, hyaluronic acid (HA) hydrogels are biofunctionalized with an N-cadherin mimetic peptide to mimic the pro-osteogenic niche in the endosteal space to promote the osteogenesis of human mesenchymal stem cells (hMSCs). Results show that the conjugation of the N-cadherin peptide in the HA hydrogels enhances the expression of the osteogenic marker genes in the seeded hMSCs. Furthermore, the biofunctionalized HA hydrogels promote the alkaline phosphatase activity, type I collagen deposition, and matrix mineralization by the seeded hMSCs under both in vitro and in vivo condition. We postulate that the biofunctionalized hydrogels emulates the N-cadherin-mediated homotypic cell-cell adhesion among MSCs and the "orthotypic" interaction between the osteoblasts and MSCs. These findings demonstrate that the biofunctionalized HA hydrogels provide a supportive niche microenvironment for the osteogenesis of hMSCs. |
| Persistent Identifier | http://hdl.handle.net/10722/363212 |
| ISSN | 2023 Impact Factor: 12.8 2023 SCImago Journal Rankings: 3.016 |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Zhu, Meiling | - |
| dc.contributor.author | Lin, Sien | - |
| dc.contributor.author | Sun, Yuxin | - |
| dc.contributor.author | Feng, Qian | - |
| dc.contributor.author | Li, Gang | - |
| dc.contributor.author | Bian, Liming | - |
| dc.date.accessioned | 2025-10-10T07:45:14Z | - |
| dc.date.available | 2025-10-10T07:45:14Z | - |
| dc.date.issued | 2016 | - |
| dc.identifier.citation | Biomaterials, 2016, v. 77, p. 44-52 | - |
| dc.identifier.issn | 0142-9612 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/363212 | - |
| dc.description.abstract | N-cadherin is considered to be the key factor in directing cell-cell interactions during mesenchymal condensation, which is essential to osteogenesis. In this study, hyaluronic acid (HA) hydrogels are biofunctionalized with an N-cadherin mimetic peptide to mimic the pro-osteogenic niche in the endosteal space to promote the osteogenesis of human mesenchymal stem cells (hMSCs). Results show that the conjugation of the N-cadherin peptide in the HA hydrogels enhances the expression of the osteogenic marker genes in the seeded hMSCs. Furthermore, the biofunctionalized HA hydrogels promote the alkaline phosphatase activity, type I collagen deposition, and matrix mineralization by the seeded hMSCs under both in vitro and in vivo condition. We postulate that the biofunctionalized hydrogels emulates the N-cadherin-mediated homotypic cell-cell adhesion among MSCs and the "orthotypic" interaction between the osteoblasts and MSCs. These findings demonstrate that the biofunctionalized HA hydrogels provide a supportive niche microenvironment for the osteogenesis of hMSCs. | - |
| dc.language | eng | - |
| dc.relation.ispartof | Biomaterials | - |
| dc.subject | Bio-functionalization of biomaterials | - |
| dc.subject | Hyaluronic acid hydrogels | - |
| dc.subject | Mesenchymal stem cells | - |
| dc.subject | Tissue engineering | - |
| dc.title | Hydrogels functionalized with N-cadherin mimetic peptide enhance osteogenesis of hMSCs by emulating the osteogenic niche | - |
| dc.type | Article | - |
| dc.description.nature | link_to_subscribed_fulltext | - |
| dc.identifier.doi | 10.1016/j.biomaterials.2015.10.072 | - |
| dc.identifier.pmid | 26580785 | - |
| dc.identifier.scopus | eid_2-s2.0-84949256833 | - |
| dc.identifier.volume | 77 | - |
| dc.identifier.spage | 44 | - |
| dc.identifier.epage | 52 | - |
| dc.identifier.eissn | 1878-5905 | - |
