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Topographic variation in redifferentiation capacity of chondrocytes in the adult human knee joint.

Hanna Stenhamre (Institutionen för biomedicin, avdelningen för klinisk kemi och transfusionsmedicin ; Institutionen för kemi- och bioteknik, Polymerteknologi) ; K Slynarski ; C Petrén ; Tommi Tallheden ; Anders Lindahl
Osteoarthritis and cartilage / OARS, Osteoarthritis Research Society (1522-9653). Vol. 16 (2008), 11, p. 1356-62.
[Artikel, refereegranskad vetenskaplig]

OBJECTIVES: The aim of this study was to investigate the topographic variation in matrix production and cell density in the adult human knee joint. Additionally, we have examined the redifferentiation potential of chondrocytes expanded in vitro from the different locations. METHOD: Full thickness cartilage-bone biopsies were harvested from seven separate anatomical locations of healthy knee joints from deceased adult human donors. Chondrocytes were isolated, expanded in vitro and redifferentiated in a pellet mass culture. Biochemical analysis of total collagen, proteoglycans and cellular content as well as histology and immunohistochemistry were performed on biopsies and pellets. RESULTS: In the biochemical analysis of the biopsies, we found lower proteoglycan to collagen (GAG/HP) ratio in the non-weight bearing (NWB) areas compared to the weight bearing (WB) areas. The chondrocytes harvested from different locations in femur showed a significantly better attachment and proliferation ability as well as good post-expansion chondrogenic capacity in pellet mass culture compared with the cells harvested from tibia. CONCLUSION: These results demonstrate that there are differences in extra cellular content within the adult human knee in respect to GAG/HP ratio. Additionally, the data show that clear differences between chondrocytes harvested from femur and tibia from healthy human knee joints exist and that the differences are not completely abolished during the process of de- and redifferentiation. These findings emphasize the importance of the understanding of topographic variation in articular cartilage biology when approaching new cartilage repair strategies.

Denna post skapades 2008-12-19. Senast ändrad 2017-06-30.
CPL Pubid: 82329


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Institutioner (Chalmers)

Institutionen för biomedicin, avdelningen för klinisk kemi och transfusionsmedicin (GU)
Institutionen för kemi- och bioteknik, Polymerteknologi (2005-2014)


Klinisk fysiologi
Medicinsk cellbiologi

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