Publications by authors named "Haneen A Abusharkh"

This work is focused on designing an easy-to-use novel perfusion system for articular cartilage (AC) tissue engineering and using it to elucidate the mechanism by which interstitial shear upregulates matrix synthesis by articular chondrocytes (AChs). Porous chitosan-agarose (CHAG) scaffolds were synthesized and compared to bulk agarose (AG) scaffolds. Both scaffolds were seeded with osteoarthritic human AChs and cultured in a novel perfusion system with a medium flow velocity of 0.

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The evaluation of specific protein content in engineered tissues provides a gateway for developing regenerative medicine treatments. Since collagen type II, the major component of articular cartilage, is critical for the blossoming field of articular cartilage tissue engineering, the interest in this protein is growing rapidly. Accordingly, the need for quantification of collagen type II is increasing as well.

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Osteoarthritis (OA) patients undergo cartilage degradation and experience painful joint swelling. OA symptoms are caused by inflammatory molecules and the upregulation of catabolic genes leading to the breakdown of cartilage extracellular matrix (ECM). Here, we investigate the effects of gallic acid (GA) and mechanical stretching on the expression of anabolic and catabolic genes and restoring ECM production by osteoarthritic human articular chondrocytes (hAChs) cultured in monolayers.

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Article Synopsis
  • Conventional treatments for osteoarthritis fail to regenerate cartilage, prompting exploration of tissue engineering techniques like autologous chondrocyte implantation that inject cells to repair cartilage lesions.
  • This study aims to enhance the effectiveness of chondrocyte implantation by utilizing human adipose-derived stem cells to reduce the required number of chondrocytes, improve cell resilience under stress, and increase the production of vital extracellular matrix proteins.
  • Findings suggest that up to 75% of chondrocytes can be substituted with stem cells while still improving collagen and glycosaminoglycan production, achieving significant enhancements in these metrics without harming cell viability.
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