Heterogeneous three-dimensional strain fields during unconfined cyclic compression in bovine articular cartilage explants

2005 ◽  
Vol 23 (6) ◽  
pp. 1390-1398 ◽  
Author(s):  
C. P. Neu ◽  
M. L. Hull ◽  
J. H. Walton
2003 ◽  
Vol 44 (3-4) ◽  
pp. 154-159 ◽  
Author(s):  
Monica De Mattei ◽  
Michela Pasello ◽  
Agnese Pellati ◽  
Giordano Stabellini ◽  
Leo Massari ◽  
...  

1998 ◽  
Vol 37 (3-4) ◽  
pp. 277-293 ◽  
Author(s):  
Gavin m. Winter ◽  
C. Anthony Poole ◽  
Mirna Z. Ilic ◽  
Jacqueline M. Ross ◽  
H. Clem Robinson ◽  
...  

2005 ◽  
Vol 53 (9) ◽  
pp. 1109-1119 ◽  
Author(s):  
Kyle D. Jadin ◽  
Benjamin L. Wong ◽  
Won C. Bae ◽  
Kelvin W. Li ◽  
Amanda K. Williamson ◽  
...  

Articular cartilage is a heterogeneous tissue, with cell density and organization varying with depth from the surface. The objectives of the present study were to establish a method for localizing individual cells in three-dimensional (3D) images of cartilage and quantifying depth-associated variation in cellularity and cell organization at different stages of growth. Accuracy of nucleus localization was high, with 99% sensitivity relative to manual localization. Cellularity (million cells per cm3) decreased from 290, 310, and 150 near the articular surface in fetal, calf, and adult samples, respectively, to 120, 110, and 50 at a depth of 1.0 mm. The distance/angle to the nearest neighboring cell was 7.9 μm/31°, 7.1 μm/31°, and 9.1 μm/31° for cells at the articular surface of fetal, calf, and adult samples, respectively, and increased/decreased to 11.6 μm/31°, 12.0 μm/30°, and 19.2 μm/25° at a depth of 0.7 mm. The methodologies described here may be useful for analyzing the 3D cellular organization of cartilage during growth, maturation, aging, degeneration, and regeneration.


2003 ◽  
Vol 44 (3) ◽  
pp. 154-159 ◽  
Author(s):  
Monica De Mattei ◽  
Michela Pasello ◽  
Agnese Pellati ◽  
Giordano Stabellini ◽  
Leo Massari ◽  
...  

2011 ◽  
Vol 133 (4) ◽  
Author(s):  
S. M. T. Chan ◽  
C. P. Neu ◽  
K. Komvopoulos ◽  
A. H. Reddi ◽  
P. E. Di Cesare

Friction and wear of four common orthopaedic biomaterials, alumina (Al2O3), cobalt-chromium (CoCr), stainless steel (SS), and crosslinked ultra-high-molecular-weight polyethylene (UHMWPE), sliding against bovine articular cartilage explants were investigated by reciprocating sliding, nanoscale friction and roughness measurements, protein wear assays, and histology. Under the experimental conditions of the present study, CoCr yielded the largest increase in cartilage friction coefficient, largest amount of protein loss, and greatest change in nanoscale friction after sliding against cartilage. UHMWPE showed the lowest cartilage friction coefficient, least amount of protein loss, and insignificant changes in nanoscale friction after sliding. Although the results are specific to the testing protocol and surface roughness of the examined biomaterials, they indicate that CoCr tends to accelerate wear of cartilage, whereas the UHMWPE shows the best performance against cartilage. This study also shows that the surface characteristics of all biomaterials must be further improved to achieve the low friction coefficient of the cartilage/cartilage interface.


2002 ◽  
Vol 50 (10) ◽  
pp. 1313-1323 ◽  
Author(s):  
Ghada A. Nofal ◽  
Cheryl B. Knudson

The proteoglycan-rich extracellular matrix (ECM) directly associated with the cells of articular cartilage is anchored to the chondrocyte plasma membrane via interaction with the hyaluronan receptor CD44. The cytoplasmic tail of CD44 interacts with the cortical cytoskeleton. The objective of this study was to determine the role of the actin cytoskeleton in CD44-mediated matrix assembly by chondrocytes and cartilage matrix retention and homeostasis. Adult bovine articular cartilage tissue slices and isolated chondrocytes were treated with latrunculin or cytochalasin. Tissues were processed for histology and chondrocytes were examined for CD44 expression and pericellular matrix assembly. Treatments that disrupt the actin cytoskeleton reduced chondrocyte pericellular matrix assembly and the retention of proteoglycan within cartilage explants. There was enhanced detection of a neoepitope resulting from proteolysis of aggrecan. Cytoskeletal disruption did not reduce CD44 expression, as monitored by flow cytometry, but detergent extraction of CD44 was enhanced and hyaluronan binding was decreased. Thus, disruption of the cytoskeleton reduces the anchorage of CD44 in the chondrocyte membrane and the capacity of CD44 to bind its ligand. The results suggest that cytoskeletal disruption within cartilage uncouples chondrocytes from the matrix, resulting in altered metabolism and deleterious changes in matrix structure.


1995 ◽  
Vol 44 (S2) ◽  
pp. S119-S120 ◽  
Author(s):  
S. Wertheimer ◽  
S. Katz ◽  
K. Rowan ◽  
A. Lugo ◽  
W. Levin ◽  
...  

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