Local stimulation of proteoglycan synthesis in articular cartilage explants by dynamic compression in vitro

1992 ◽  
Vol 10 (5) ◽  
pp. 610-620 ◽  
Author(s):  
Jyrki J. Parkkinen ◽  
Mikko J. Lammi ◽  
Heikki J. Helminen ◽  
Markku Tammi
Keyword(s):  
Articular Cartilage ◽  
Dynamic Compression ◽  
Cartilage Explants ◽  
Proteoglycan Synthesis ◽  
Local Stimulation ◽  
Stimulation Of

Mechanical compression alters proteoglycan deposition and matrix deformation around individual cells in cartilage explants

1998 ◽  
Vol 111 (5) ◽  
pp. 573-583
Author(s):  
T.M. Quinn ◽  
A.J. Grodzinsky ◽  
M.D. Buschmann ◽  
Y.J. Kim ◽  
E.B. Hunziker
Keyword(s):  
Morphological Changes ◽  
Dynamic Compression ◽  
Compressive Strain ◽  
Cell Length ◽  
Cartilage Explants ◽  
Proteoglycan Synthesis ◽  
Length Scale ◽  
Mechanical Compression ◽  
Static Compression ◽  
Associated Matrix

We have used new techniques of cell-length scale quantitative autoradiography to assess matrix synthesis, deposition, and deformation around individual chondrocytes in mechanically compressed cartilage explants. Our objectives were to: (1) quantify the effects of static and dynamic compression on the deposition of newly synthesized proteoglycans into cell-associated and further-removed matrices; (2) measure cell-length scale matrix strains and morphological changes of the cell and matrix associated with tissue compression; and (3) relate microscopic physical stimuli to changes in proteoglycan synthesis as functions of compression level and position within mechanically compressed explants. Results indicate a high degree of structural organization in the extracellular matrix, with the pericellular matrix associated with the most rapid rates of proteoglycan deposition, and greatest sensitivity to mechanical compression. Static compression could stimulate directional deposition of secreted proteoglycans around chondrocytes, superimposed on an inhibition of proteoglycan synthesis; these events followed trends for compressive strain in the cell-associated matrix. Conversely, proteoglycan synthesis and pericellular deposition was stimulated by dynamic compression. Results suggest that cell-matrix interactions in the cell-associated matrix may be a particularly important aspect of the chondrocyte response to mechanical compression, possibly involving macromolecular transport limitations and morphological changes associated with fluid flow and local compaction of the matrix around cells.

scholarly journals Effect of GCSB-5, a Herbal Formulation, on Monosodium Iodoacetate-Induced Osteoarthritis in Rats

2012 ◽  
Vol 2012 ◽  
pp. 1-11 ◽  
Author(s):  
Joon-Ki Kim ◽  
Sang-Won Park ◽  
Jung-Woo Kang ◽  
Yu-Jin Kim ◽  
Sung Youl Lee ◽  
...  
Keyword(s):  
Articular Cartilage ◽  
Protein Expression ◽  
Nuclear Factor Κb ◽  
Interleukin 10 ◽  
Cartilage Explants ◽  
Therapeutic Effects ◽  
Monosodium Iodoacetate ◽  
Factor Α

Therapeutic effects of GCSB-5 on osteoarthritis were measured by the amount of glycosaminoglycan in rabbit articular cartilage explantsin vitro, in experimental osteoarthritis induced by intra-articular injection of monoiodoacetate in ratsin vivo. GCSB-5 was orally administered for 28 days.In vitro, GCSB-5 inhibited proteoglycan degradation. GCSB-5 significantly suppressed the histological changes in monoiodoacetate-induced osteoarthritis. Matrix metalloproteinase (MMP) activity, as well as, the levels of serum tumor necrosis factor-α, cyclooxygenase-2, inducible nitric oxide synthase protein, and mRNA expressions were attenuated by GCSB-5, whereas the level of interleukin-10 was potentiated. By GCSB-5, the level of nuclear factor-κB p65 protein expression was significantly attenuated but, on the other hand, the level of inhibitor of κB-α protein expression was increased. These results indicate that GCSB-5 is a potential therapeutic agent for the protection of articular cartilage against progression of osteoarthritis through inhibition of MMPs activity, inflammatory mediators, and NF-κB activation.

MUSCLE-INDUCED PATELLOFEMORAL JOINT LOADING RAPIDLY AFFECTS CARTILAGE mRNA LEVELS IN A SITE SPECIFIC MANNER

2004 ◽  
Vol 08 (01) ◽  
pp. 1-12 ◽  
Author(s):  
Andrea L. Clark ◽  
Linda Mills ◽  
David A Hart ◽  
Walter Herzog
Keyword(s):  
Articular Cartilage ◽  
Mechanical Loading ◽  
Patellofemoral Joint ◽  
Mrna Level ◽  
Recovery Period ◽  
Cartilage Explants ◽  
Mrna Levels ◽  
Biological Responses

Mechanical loading of articular cartilage affects the synthesis and degradation of matrix macromolecules. Much of the work in this area has involved mechanical loading of articular cartilage explants or cells in vitro and assessing biological responses at the mRNA and protein levels. In this study, we developed a new experimental technique to load an intact patellofemoral joint in vivo using muscle stimulation. The articular cartilages were cyclically loaded for one hour in a repeatable and measurable manner. Cartilage was harvested from central and peripheral regions of the femoral groove and patella, either immediately after loading or after a three hour recovery period. Total RNA was isolated from the articular cartilage and biological responses were assessed on the mRNA level using the reverse transcriptase-polymerase chain reaction. Articular cartilage from intact patellofemoral joints demonstrated heterogeneity at the mRNA level for six of the genes assessed independent of the loading protocol. Cyclical loading of cartilage in its native environment led to alterations in mRNA levels for a subset of molecules when assessed immediately after the loading period. However, the increases in TIMP-1 and decreases in bFGF mRNA levels were transient; being present immediately after load application but not after a three hour recovery period.

Effects of sodium hyaluronate and methylprednisolone acetate on proteoglycan synthesis in equine articular cartilage explants

2005 ◽  
Vol 66 (1) ◽  
pp. 48-53 ◽  
Author(s):  
Aimie J. Doyle ◽  
Allison A. Stewart ◽  
Peter D. Constable ◽  
Jo Ann C. Eurell ◽  
David E. Freeman ◽  
...  
Keyword(s):  
Articular Cartilage ◽  
Sodium Hyaluronate ◽  
Cartilage Explants ◽  
Proteoglycan Synthesis ◽  
Methylprednisolone Acetate

scholarly journals Simulating the Growth of Articular Cartilage Explants in a Permeation Bioreactor to Aid in Experimental Protocol Design

2009 ◽  
Vol 131 (4) ◽  
Author(s):  
Timothy P. Ficklin ◽  
Andrew Davol ◽  
Stephen M. Klisch
Keyword(s):  
Finite Element ◽  
Steady State ◽  
Articular Cartilage ◽  
Element Model ◽  
Cartilage Explants ◽  
Solid Matrix ◽  
Cartilage Growth ◽  
Growth Laws ◽  
Competing Hypotheses

Recently a cartilage growth finite element model (CGFEM) was developed to solve nonhomogeneous and time-dependent growth boundary-value problems (Davol et al., 2008, “A Nonlinear Finite Element Model of Cartilage Growth,” Biomech. Model. Mechanobiol., 7, pp. 295–307). The CGFEM allows distinct stress constitutive equations and growth laws for the major components of the solid matrix, collagens and proteoglycans. The objective of the current work was to simulate in vitro growth of articular cartilage explants in a steady-state permeation bioreactor in order to obtain results that aid experimental design. The steady-state permeation protocol induces different types of mechanical stimuli. When the specimen is initially homogeneous, it directly induces homogeneous permeation velocities and indirectly induces nonhomogeneous solid matrix shear stresses; consequently, the steady-state permeation protocol is a good candidate for exploring two competing hypotheses for the growth laws. The analysis protocols were implemented through the alternating interaction of the two CGFEM components: poroelastic finite element analysis (FEA) using ABAQUS and a finite element growth routine using MATLAB. The CGFEM simulated 12 days of growth for immature bovine articular cartilage explants subjected to two competing hypotheses for the growth laws: one that is triggered by permeation velocity and the other by maximum shear stress. The results provide predictions for geometric, biomechanical, and biochemical parameters of grown tissue specimens that may be experimentally measured and, consequently, suggest key biomechanical measures to analyze as pilot experiments are performed. The combined approach of CGFEM analysis and pilot experiments may lead to the refinement of actual experimental protocols and a better understanding of in vitro growth of articular cartilage.

Glycosaminoglycan and Collagen Remodeling During In Vitro Dynamic Compression of Articular Cartilage: Experiments and Finite Element Modeling

2013 ◽  
Author(s):  
Kevin A. Yamauchi ◽  
Christopher B. Raub ◽  
Albert C. Chen ◽  
Robert L. Sah ◽  
Scott J. Hazelwood ◽  
...  
Keyword(s):  
Articular Cartilage ◽  
Dynamic Compression ◽  
Fluid Velocity ◽  
Biomechanical Properties ◽  
Mechanical Stimuli ◽  
Unconfined Compression ◽  
Growth Data ◽  
Collagen Remodeling ◽  
Continuum Mixture Model

The biomechanical properties of articular cartilage (AC) can be altered by chemical and mechanical stimuli. Dynamic unconfined compression (UCC) has been shown to increase biosynthesis at moderate strain amplitudes (1–4%) and frequencies from 0.01Hz. to 0.1Hz [1]. Furthermore, interstitial fluid velocity and maximum principle strain have been proposed as candidates for controlling glycosaminoglycan (GAG) and collagen (COL) remodeling, respectively [2,3]. The goal of this study was to integrate in vitro growth data, including biochemical and microstructural properties, into a computational continuum mixture model to elucidate potential mechanical triggers for AC tissue remodeling.

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