دورية أكاديمية

The chondrogenic differentiation potential of dental pulp stem cells

التفاصيل البيبلوغرافية
العنوان: The chondrogenic differentiation potential of dental pulp stem cells
المؤلفون: A Longoni, L Utomo, IEM van Hooijdonk, GKP Bittermann, VC Vetter, EC Kruijt Spanjer, J Ross, AJWP Rosenberg, D Gawlitta
المصدر: European Cells & Materials, Vol 39, Pp 121-135 (2020)
بيانات النشر: Forum Multimedia Publishing LLC, 2020.
سنة النشر: 2020
المجموعة: LCC:Diseases of the musculoskeletal system
LCC:Orthopedic surgery
مصطلحات موضوعية: cartilage regeneration, hyaline, fibrous, neural-crest-derived stem cells, adult stem cell differentiation., Diseases of the musculoskeletal system, RC925-935, Orthopedic surgery, RD701-811
الوصف: Dental pulp stem cells (DPSCs) are particularly promising for tissue engineering (TE) due to the ease of their isolation procedure, great expansion potential and capability to differentiate towards several cell types of the mesodermal, ectodermal and endodermal lineages. Although several studies hint that DPSCs exhibit potential for cartilage tissue formation, the chondrogenic potential of DPSCs has only been marginally explored. Thus, the aim of the present study was to closely investigate the chondrogenic differentiation capacity of DPSCs for TE applications. More specifically, the potential of DPSCs for engineering hyaline and fibrous cartilage was determined. DPSCs obtained from 7 human molars were expanded and chondrogenically differentiated in a 3D pellet culture model. After 21 d of differentiation with chondrogenic stimuli, DPSCs displayed glycosaminoglycan, aggrecan and limited collagen type II deposition. Cells presented an elongated morphology and produced a collagen-rich extracellular matrix, with a predominance of collagen type I in most of the samples, a characteristic of fibrous cartilage tissue. Variations in the administration periods of several chondro-inductive growth factors, including transforming growth factor beta 3, bone morphogenetic protein-2, -6, -7 and insulin-like growth factor-1, did not increase glycosaminoglycan or collagen type II deposition, typical markers of hyaline cartilage tissue. Furthermore, DPSCs could not be stimulated to go into hypertrophic chondrogenesis. These results indicated that under a large variety of chondro-inductive culture conditions, DPSCs could form fibrocartilaginous tissues but not hyaline cartilage. Thus, DPSCs represent a valuable cell source for the regeneration of fibrocartilage in joints.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1473-2262
Relation: https://www.ecmjournal.org/papers/vol039/pdf/v039a08.pdf; https://doaj.org/toc/1473-2262
DOI: 10.22203/eCM.v039a08
URL الوصول: https://doaj.org/article/de0260dfb39d471d83bef7728d4dbcb4
رقم الأكسشن: edsdoj.0260dfb39d471d83bef7728d4dbcb4
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14732262
DOI:10.22203/eCM.v039a08