3D Bioprinted Silk-Based In Vitro Osteochondral Model for Osteoarthritis Therapeutics

被引:14
作者
Singh, Yogendra Pratap [1 ]
Moses, Joseph Christakiran [1 ]
Bandyopadhyay, Ashutosh [1 ]
Mandal, Biman B. [1 ,2 ,3 ]
机构
[1] Indian Inst Technol Guwahati, Dept Biosci & Bioengn, Gauhati 781039, Assam, India
[2] Indian Inst Technol Guwahati, Ctr Nanotechnol, Gauhati 781039, Assam, India
[3] Indian Inst Technol Guwahati, Sch Hlth Sci & Technol, Gauhati 781039, Assam, India
关键词
3D bioprinting; drug screening platforms; in vitro disease models; osteoarthritis; osteochondral tissue engineering; NF-KAPPA-B; NECROSIS-FACTOR-ALPHA; HUMAN ARTICULAR CHONDROCYTES; GENE-EXPRESSION; TNF-ALPHA; CARTILAGE; CELECOXIB; BONE; SCAFFOLDS; DIACEREIN;
D O I
10.1002/adhm.202200209
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
3D bioprinting of osteochondral tissue offers unique opportunities for enabling precise pharmacological interventions in osteoarthritis (OA). The current study investigates the screening potential of anti-inflammatory drugs using bioprinted inflamed human osteochondral units. The biomimetic hierarchical geometry is bioprinted using silk-based bioinks encapsulating pre-differentiated stem cells, creating an in vitro model. Inflammation is stimulated in the model, using tumor necrosis factor-alpha and Interleukin-1 beta pro-inflammatory cytokines. The resultant degeneration, akin to OA, is flagged by key markers like sulfated glycosaminoglycan, collagen, alkaline phosphatase, and downregulation of osteochondral transcript levels. In the next step, the screening of anti-inflammatory drugs is validated using celecoxib and rhein. Consequently, in the inflamed constructs, the initial upregulation of the key inflammatory mediators (nitric oxide, Prostaglandin E2), is subsequently downregulated, post-drug treatment. In addition, catabolic markers (matrix metalloproteinases and aggrecanase-1), indicative of hypertrophic and apoptosing chondrocytes, are significantly downregulated in the treatment groups; while the transcript and protein levels required for osteochondral health are attenuated. Therefore, the in vitro model mimicks the inflammation in the early stages of OA, and corroborates a potential high-throughput platform for screening novel anti-inflammatory drugs in OA therapeutics.
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页数:15
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