Ultrasound-derived mechanical stimulation of cell-laden collagen hydrogels for bone repair

被引:14
作者
Assanah, Fayekah [1 ,2 ]
Grassie, Kevin [1 ,2 ]
Anderson, Hanna [1 ,2 ]
Xin, Xiaonan [3 ]
Rowe, David [3 ]
Khan, Yusuf [1 ,2 ,4 ,5 ]
机构
[1] Univ Connecticut, Dept Biomed Engn, Storrs, CT USA
[2] UCONN Hlth, Connecticut Convergence Inst Translat Regenerat En, Farmington, CT USA
[3] UCONN Sch Dent Med, Ctr Regenerat Med & Skeletal Dev, Farmington, CT USA
[4] UCONN Hlth, Dept Orthoped Surg, Farmington, CT USA
[5] UCONN Hlth, Connecticut Convergence Inst Translat Regenerat En, MC3711,Room E7052,263 Farmington Ave, Farmington, CT 06030 USA
基金
美国国家卫生研究院;
关键词
acoustic radiation force; cell therapy; collagen; hydrogel; ultrasound; INTENSITY PULSED ULTRASOUND; MESENCHYMAL STEM-CELLS; PROSTAGLANDIN E-2 PRODUCTION; ACOUSTIC RADIATION FORCE; FLUID-FLOW; GENE-EXPRESSION; SHEAR-STRESS; IN-VITRO; OSTEOGENIC DIFFERENTIATION; CELL/HYDROGEL CONSTRUCTS;
D O I
10.1002/jbm.a.37508
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cell therapy is emerging as an effective treatment strategy for many diseases. Here we describe a novel approach to bone tissue repair that combines hydrogel-based cell therapy with low intensity pulsed ultrasound (LIPUS), an FDA approved treatment for fracture repair. Bone marrow-derived stromal cells (BMSCs) have been encapsulated in type I collagen hydrogels and mechanically stimulated using LIPUS-derived acoustic radiation force (ARF). We observed the expression and upward trend of load-sensitive, osteoblast-specific markers and determined that the extent of cell response is dependent on an optimal combination of both hydrogel stiffness and ARF intensity. Specifically, cells encapsulated in hydrogels of optimal stiffness respond at the onset of ultrasound by upregulating early bone-sensitive markers such as calcium, cyclooxygenase-2, and prostaglandin E-2, and later by supporting mineralized tissue formation after 21 days of culture. In vivo evaluation of a critical size calvarial defect in NOD scid gamma (NSG) mice indicated that the implantation of BMSC-laden hydrogels of optimal stiffness improved healing of calvarial defects after daily administration of ARF over 4 weeks. Collectively, these findings validate the efficacy of our system of localized cell delivery for treating bone defects where undifferentiated BMSCs are induced to the osteoblastic lineage. Further, in vivo healing may be enhanced via non-invasive transdermal mechanical stimulation of implanted cells using ARF.
引用
收藏
页码:1200 / 1215
页数:16
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