Investigation of multiphasic 3D-bioplotted scaffolds for site-specific chondrogenic and osteogenic differentiation of human adipose-derived stem cells for osteochondral tissue engineering applications

被引:32
作者
Mellor, Liliana F. [1 ]
Nordberg, Rachel C. [1 ,2 ]
Huebner, Pedro [3 ]
Mohiti-Asli, Mahsa [1 ]
Taylor, Michael A. [1 ]
Efird, William [4 ]
Oxford, Julia T. [5 ]
Spang, Jeffrey T. [4 ]
Shirwaiker, Rohan A. [1 ,3 ]
Loboa, Elizabeth G. [2 ]
机构
[1] Joint Dept Biomed Engn Univ North Carolina Chapel, Raleigh, NC USA
[2] Univ Missouri, Coll Engn, Dept Biomed Biol & Chem Engn, Columbia, MO USA
[3] North Carolina State Univ, Edward P Fitts Dept Ind & Syst Engn, Raleigh, NC 27695 USA
[4] Univ N Carolina, Sch Med, Dept Orthopaed, Chapel Hill, NC 27515 USA
[5] Boise State Univ, Biomol Res Ctr, Boise, ID 83725 USA
基金
美国国家科学基金会; 美国国家卫生研究院; 美国国家航空航天局;
关键词
3D-printing; chondrogenic differentiation; human adipose derived stem cells; osteochondral; osteogenic differentiation; IN-VITRO GENERATION; HUMAN BONE-MARROW; EXTRACELLULAR-MATRIX; CURRENT STRATEGIES; CARTILAGE REPAIR; REGENERATION; OSTEOARTHRITIS; INDUCTION; VIABILITY; DEFECTS;
D O I
10.1002/jbm.b.34542
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Osteoarthritis is a degenerative joint disease that limits mobility of the affected joint due to the degradation of articular cartilage and subchondral bone. The limited regenerative capacity of cartilage presents significant challenges when attempting to repair or reverse the effects of cartilage degradation. Tissue engineered medical products are a promising alternative to treat osteochondral degeneration due to their potential to integrate into the patient's existing tissue. The goal of this study was to create a scaffold that would induce site-specific osteogenic and chondrogenic differentiation of human adipose-derived stem cells (hASC) to generate a full osteochondral implant. Scaffolds were fabricated using 3D-bioplotting of biodegradable polycraprolactone (PCL) with either beta-tricalcium phosphate (TCP) or decellularized bovine cartilage extracellular matrix (dECM) to drive site-specific hASC osteogenesis and chondrogenesis, respectively. PCL-dECM scaffolds demonstrated elevated matrix deposition and organization in scaffolds seeded with hASC as well as a reduction in collagen I gene expression. 3D-bioplotted PCL scaffolds with 20% TCP demonstrated elevated calcium deposition, endogenous alkaline phosphatase activity, and osteopontin gene expression. Osteochondral scaffolds comprised of hASC-seeded 3D-bioplotted PCL-TCP, electrospun PCL, and 3D-bioplotted PCL-dECM phases were evaluated and demonstrated site-specific osteochondral tissue characteristics. This technique holds great promise as cartilage morbidity is minimized since autologous cartilage harvest is not required, tissue rejection is minimized via use of an abundant and accessible source of autologous stem cells, and biofabrication techniques allow for a precise, customizable methodology to rapidly produce the scaffold.
引用
收藏
页码:2017 / 2030
页数:14
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