Seven million people suffer bone fractures annually in the U.S. Musculoskeletal conditions cost $215 billion/year. These numbers are increasing dramatically as the population ages. Calcium phosphate cement (CPC) can be molded and set in-situ to form hydroxyapatite, is osteoconductive, and can be resorbed and replaced by new bone. However, the low strength of CPC limits its use to non-stress locations. The parent grant investigates compositional and microstructural tailoring to improve injectability, strength and resorption;optimizes chitosan content;develops non-rigid CPC with high-strain and anti-washout;models growth factor release as a function of pore volume fraction and time;and performs animal study on CPC resorption and the effects of microstructural design, and animal study on bone regeneration and the effects of single and multiple growth factors and MSCs delivered. However, the parent grant does not include the use of electrospun nanofibers, nor human umbilical cord mesenchymal stem cells (hUCMSCs). The objectives of this competitive revision supplement are to: (1) Develop novel, injectable nanofiber-CPC scaffolds with increased load-bearing capability and enhanced stem cell attachment and function for bone repair;(2) establish relationships between nanofibers and scaffold properties, and between nanofibers and stem cell attachment, proliferation, differentiation, and in vivo bone regeneration;(3) determine whether hUCMSCs are more superior than adult bone marrow-derived hMSCs in bone regeneration, when delivered via nanofiber-CPC scaffold.
Aim 1 will develop electrospun nanofiber-CPC as injectable, load-bearing, and bioactive scaffold.
Aim 2 will study the effect of nanofiber-CPC scaffold on hMSC and hUMCSC proliferation and differentiation.
Aim 3 will investigate the effects of hMSC and hUCMSC delivery via nanofiber-CPC on bone regeneration in animal model. This project is expected to demonstrate, for the first time, that hUCMSCs delivered via novel nanofiber-CPC scaffold are more superior in osteogenesis and bone regeneration, than bone marrow-derived hMSCs. These findings will potentially have a highly significant impact on stem cell-based tissue engineering and future clinical treatments. The new injectable, strong and macroporous nanofiber-CPC scaffolds with stem cell and growth factor delivery are expected to have a wide range of dental, craniofacial and orthopedic applications, with greatly enhanced bone regeneration to improve the health and quality of life for millions of people.

Public Health Relevance

This project will develop the first injectable, moderate load-bearing, macroporous, bone-mimicking nanofiber-apatite scaffolds with stem cell and multiple growth factor delivery, and will study bone regeneration in animal model. Potential applications include dental, craniofacial and orthopedic repairs. They include maxillofacial reconstruction using the moldable scaffold to achieve shaping and esthetics, and minimally-invasive surgeries such as filling and strengthening osteoporotic bone lesions at risk for fracture, with greatly enhanced bone healing and regeneration to improve the health and quality of life for millions of people.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
3R01DE014190-07A1S1
Application #
7811914
Study Section
Special Emphasis Panel (ZRG1-MOSS-K (95))
Program Officer
Drummond, James
Project Start
2009-09-23
Project End
2011-08-31
Budget Start
2009-09-23
Budget End
2011-08-31
Support Year
7
Fiscal Year
2009
Total Cost
$416,624
Indirect Cost
Name
University of Maryland Baltimore
Department
Dentistry
Type
Schools of Dentistry
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
Qin, Wei; Gao, Xianling; Ma, Tao et al. (2018) Metformin Enhances the Differentiation of Dental Pulp Cells into Odontoblasts by Activating AMPK Signaling. J Endod 44:576-584
Xia, Yang; Chen, Huimin; Zhang, Feimin et al. (2018) Gold nanoparticles in injectable calcium phosphate cement enhance osteogenic differentiation of human dental pulp stem cells. Nanomedicine 14:35-45
Chen, Wenchuan; Liu, Xian; Chen, Qianmin et al. (2018) Angiogenic and osteogenic regeneration in rats via calcium phosphate scaffold and endothelial cell co-culture with human bone marrow mesenchymal stem cells (MSCs), human umbilical cord MSCs, human induced pluripotent stem cell-derived MSCs and human embry J Tissue Eng Regen Med 12:191-203
Xu, Hockin Hk; Wang, Ping; Wang, Lin et al. (2017) Calcium phosphate cements for bone engineering and their biological properties. Bone Res 5:17056
Qin, Wei; Huang, Qi-Ting; Weir, Michael D et al. (2017) Alcohol Inhibits Odontogenic Differentiation of Human Dental Pulp Cells by Activating mTOR Signaling. Stem Cells Int 2017:8717454
Liu, Xian; Chen, Wenchuan; Zhang, Chi et al. (2017) Co-Seeding Human Endothelial Cells with Human-Induced Pluripotent Stem Cell-Derived Mesenchymal Stem Cells on Calcium Phosphate Scaffold Enhances Osteogenesis and Vascularization in Rats. Tissue Eng Part A 23:546-555
Wang, Lin; Zhang, Chi; Li, Chunyan et al. (2016) Injectable calcium phosphate with hydrogel fibers encapsulating induced pluripotent, dental pulp and bone marrow stem cells for bone repair. Mater Sci Eng C Mater Biol Appl 69:1125-36
Wang, Ping; Song, Yang; Weir, Michael D et al. (2016) A self-setting iPSMSC-alginate-calcium phosphate paste for bone tissue engineering. Dent Mater 32:252-63
Wang, Lin; Wang, Ping; Weir, Michael D et al. (2016) Hydrogel fibers encapsulating human stem cells in an injectable calcium phosphate scaffold for bone tissue engineering. Biomed Mater 11:065008
Wang, Ping; Liu, Xian; Zhao, Liang et al. (2015) Bone tissue engineering via human induced pluripotent, umbilical cord and bone marrow mesenchymal stem cells in rat cranium. Acta Biomater 18:236-48

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