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Substrate porosity enhances chondrocyte attachment, spreading, and cartilage tissue formation in vitro
Author(s) -
Spiteri C. G.,
Pilliar R. M.,
Kandel R. A.
Publication year - 2006
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.30746
Subject(s) - chondrocyte , materials science , cartilage , substrate (aquarium) , biomaterial , tissue engineering , biophysics , porosity , extracellular matrix , biomedical engineering , matrix (chemical analysis) , anatomy , composite material , nanotechnology , chemistry , biology , biochemistry , medicine , ecology
Tissue engineering is being explored as a new approach to treat damaged cartilage. As the biomaterial used may influence tissue formation, the effects of substrate geometry on chondrocyte behavior in vitro were examined. Articular chondrocytes were isolated and cultured on the surface of smooth, rough, porous‐coated, and fully porous Ti‐6Al‐4V substrates. The percentage of chondrocytes that attached to each substrate at 24 h was determined. After 24 and 72 h, chondrocytes were visualized by scanning electron microscopy and cell areas were measured. Collagen and proteoglycan accumulation within the first 24 h was determined by incorporation with [ 3 H]‐proline and [ 35 S]‐SO 4 , respectively. Chondrocyte attachment as well as matrix accumulation was enhanced as substrate surface area increased. Cell areas on the fully porous substrate were over four times greater than on any other substrate by 72 h in culture. After 8 weeks in culture, a continuous layer of cartilaginous tissue formed only on the surface of the fully porous substrate. This suggests that fully porous Ti‐6Al‐4V substrates provide the conditions that favor cartilage tissue formation by influencing cell attachment and extent of cell spreading. Understanding how substrate porosity influences chondrocyte behavior may help identify methods to further enhance cartilage tissue formation in vitro . © 2006 Wiley Periodicals, Inc. J Biomed Mater Res, 2006