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1.
J Biomater Sci Polym Ed ; 35(6): 799-822, 2024 04.
Artículo en Inglés | MEDLINE | ID: mdl-38289681

RESUMEN

Nowadays, cartilage tissue engineering (CTE) is considered important due to lack of repair of cartilaginous lesions and the absence of appropriate methods for treatment. In this study, polycaprolactone (PCL) scaffolds were fabricated by three-dimensional (3D) printing and were then coated with fibrin (F) and acellular solubilized extracellular matrix (ECM). After extracting adipose-derived stem cells (ADSCs), 3D-printed scaffolds were characterized and compared to hydrogel groups. After inducing the chondrogenic differentiation in the presence of Piascledine and comparing it with TGF-ß3 for 28 days, the expression of genes involved in chondrogenesis (AGG, COLII) and the expression of the hypertrophic gene (COLX) were examined by real-time PCR. The expression of proteins COLII and COLX was also determined by immunohistochemistry. Glycosaminoglycan was measured by toluidine blue staining. 3D-printed scaffolds clearly improved cell proliferation, viability, water absorption and compressive strength compared to the hydrogel groups. Moreover, the use of compounds such as ECM and Piascledine in the process of ADSCs chondrogenesis induction increased cartilage-specific markers and decreased the hypertrophic marker compared to TGF-ß3. In Piascledine groups, the expression of COLL II protein, COLL II and Aggrecan genes, and the amount of glycosaminoglycan showed a significant increase in the PCL/F/ECM compared to the PCL and PCL/F groups.


Asunto(s)
Células Madre Mesenquimatosas , Fitosteroles , Extractos Vegetales , Poliésteres , Andamios del Tejido , Vitamina E , Andamios del Tejido/química , Condrogénesis , Factor de Crecimiento Transformador beta3/farmacología , Cartílago , Ingeniería de Tejidos/métodos , Matriz Extracelular/metabolismo , Glicosaminoglicanos , Diferenciación Celular , Impresión Tridimensional , Hidrogeles/metabolismo , Combinación de Medicamentos
2.
Molecules ; 25(13)2020 Jul 06.
Artículo en Inglés | MEDLINE | ID: mdl-32640693

RESUMEN

It is estimated that by 2023, approximately 20% of the population of Western Europe and North America will suffer from a degenerative joint disease commonly known as osteoarthritis (OA). During the development of OA, pro-inflammatory cytokines are one of the major causes that drive the production of inflammatory mediators and thus of matrix-degrading enzymes. OA is a challenging disease for doctors due to the limitation of the joint cartilage's capacity to repair itself. Though new treatment approaches, in particular with mesenchymal stem cells (MSCs) that integrate the tissue engineering (TE) of cartilage tissue, are promising, they are not only expensive but more often do not lead to the regeneration of joint cartilage. Therefore, there is an increasing need for novel, safe, and more effective alternatives to promote cartilage joint regeneration and TE. Indeed, naturally occurring phytochemical compounds (herbal remedies) have a great anti-inflammatory, anti-oxidant, and anabolic potential, and they have received much attention for the development of new therapeutic strategies for the treatment of inflammatory diseases, including the prevention of age-related OA and cartilage TE. This paper summarizes recent research on herbal remedies and their chondroinductive and chondroprotective effects on cartilage and progenitor cells, and it also emphasizes the possibilities that exist in this research area, especially with regard to the nutritional support of cartilage regeneration and TE, which may not benefit from non-steroidal anti-inflammatory drugs (NSAIDs).


Asunto(s)
Antiinflamatorios no Esteroideos/uso terapéutico , Cartílago/efectos de los fármacos , Osteoartritis/prevención & control , Osteoartritis/terapia , Fitoquímicos/farmacología , Plantas Medicinales/química , Ingeniería de Tejidos/métodos , Curcumina/farmacología , Flavonoides/farmacología , Zingiber officinale/metabolismo , Células Madre Mesenquimatosas/metabolismo , Persea/química , Fitoquímicos/uso terapéutico , Granada (Fruta)/química , Regeneración/efectos de los fármacos , Resveratrol/farmacología , Glycine max/química
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