Spheroidal Organoids Reproduce Characteristics of Longitudinal Depth Zones in Bovine Articular Cartilage

2016 ◽  
Vol 202 (5-6) ◽  
pp. 382-392 ◽  
Author(s):  
Shuichi Mizuno ◽  
Eiichiro Takada ◽  
Naomi Fukai

Articular cartilage has multiple histologically distinct longitudinal depth zones. Development and pathogenesis occur throughout these zones. Cartilage explants, monolayer cell culture and reconstituted 3-dimensional cell constructs have been used for investigating mechanisms of pathophysiology in articular cartilage. Such models have been insufficient to reproduce zone-dependent cellular characteristics and extracellular matrix (ECM) upon investigation into cartilage development and pathogenesis. Therefore, we defined a chondrocyte spheroid model consistently formed with isolated chondrocytes from longitudinal depth zones without extrinsic materials. This spheroid showed zone-dependent characteristics of size, cartilage-specific ECM (collagen types I and II, aggrecan and keratan sulfate) and gene expressions of anabolic and catabolic molecules (matrix molecules and matrix metalloproteinase-13). In addition, the spheroid model is small enough to maintain the viability of cells and point symmetry to analyze the gradient of diffusive molecules. This spheroid organoid model will be useful to elucidate the mechanism of histogenesis and pathogenesis in articular cartilage.

Biochemistry ◽  
1994 ◽  
Vol 33 (16) ◽  
pp. 4836-4846 ◽  
Author(s):  
Gavin M. Brown ◽  
Thomas N. Huckerby ◽  
Haydn G. Morris ◽  
Beverley L. Abram ◽  
Ian A. Nieduszynski

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 ◽  
...  

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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