Winner of the Young Investigator Award of the Society for Biomaterials at the 10th World Biomaterials Congress, May 17-22, 2016, Montreal QC, Canada: Microribbon-based hydrogels accelerate stem cell-based bone regeneration in a mouse critical-size cranial defect model
Li-Hsin Han, Bogdan Conrad, Michael T. Chung, Lorenzo Deveza, Xinyi Jiang, Andrew Wang, Manish J. Butte, Michael T. Longaker, Derrick Wan and Fan Yang
Journal of biomedical materials research. Part A, v 104(6), pp 1321-1331
Stem cell-based therapies hold great promise for enhancing tissue regeneration. However, the majority of cells die shortly after transplantation, which greatly diminishes the efficacy of stem cell-based therapies. Poor cell engraftment and survival remain a major bottleneck to fully exploiting the power of stem cells for regenerative medicine. Biomaterials such as hydrogels can serve as artificial matrices to protect cells during delivery and guide desirable cell fates. However, conventional hydrogels often lack macroporosity, which restricts cell proliferation and delays matrix deposition. Here we report the use of injectable, macroporous microribbon (RB) hydrogels as stem cell carriers for bone repair, which supports direct cell encapsulation into a macroporous scaffold with rapid spreading. When transplanted in a critical-sized, mouse cranial defect model, RB-based hydrogels significantly enhanced the survival of transplanted adipose-derived stromal cells (ADSCs) (81%) and enabled up to three-fold cell proliferation after 7 days. In contrast, conventional hydrogels only led to 27% cell survival, which continued to decrease over time. MicroCT imaging showed RBs enhanced and accelerated mineralized bone repair compared to hydrogels (61% vs. 34% by week 6), and stem cells were required for bone repair to occur. These results suggest that paracrine signaling of transplanted stem cells are responsible for the observed bone repair, and enhancing cell survival and proliferation using RBs further promoted the paracrine-signaling effects of ADSCs for stimulating endogenous bone repair. We envision RB-based scaffolds can be broadly useful as a novel scaffold for enhancing stem cell survival and regeneration of other tissue types. (c) 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 1321-1331, 2016.
Winner of the Young Investigator Award of the Society for Biomaterials at the 10th World Biomaterials Congress, May 17-22, 2016, Montreal QC, Canada: Microribbon-based hydrogels accelerate stem cell-based bone regeneration in a mouse critical-size cranial defect model
Creators
Li-Hsin Han - Stanford University
Bogdan Conrad - Stanford University
Michael T. Chung - Stanford University
Lorenzo Deveza - Stanford University
Xinyi Jiang - Stanford University
Andrew Wang - Stanford University
Manish J. Butte - Stanford University
Michael T. Longaker - Stanford University
Derrick Wan - Stanford University
Fan Yang - Stanford University
Publication Details
Journal of biomedical materials research. Part A, v 104(6), pp 1321-1331
Publisher
Wiley
Number of pages
11
Grant note
1264833 / Directorate For Engineering; National Science Foundation (NSF); NSF - Directorate for Engineering (ENG)
R01DE024772 / NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Dental & Craniofacial Research (NIDCR)
R01 DE024772 / NIDCR NIH HHS; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Dental & Craniofacial Research (NIDCR)
R01GM110482 / NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of General Medical Sciences (NIGMS)
R01 GM110482 / NIGMS NIH HHS; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of General Medical Sciences (NIGMS)
Resource Type
Journal article
Language
English
Academic Unit
Mechanical Engineering and Mechanics; Drexel University
Web of Science ID
WOS:000375117200001
Scopus ID
2-s2.0-84964328556
Other Identifier
991020100183004721
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