scholarly journals Extracellular Matrix and Adhesion Molecule Gene Expression in the Normal and Injured Murine Intervertebral Disc

2019 ◽  
Vol 98 (1) ◽  
pp. 35-42 ◽  
Author(s):  
Yejia Zhang ◽  
Zuozhen Tian ◽  
Jason W. Ashley ◽  
Luqiang Wang ◽  
Robert J. Tower ◽  
...  
2008 ◽  
Vol 32 (2) ◽  
pp. 339-347 ◽  
Author(s):  
Sharada D. Vangipuram ◽  
William E. Grever ◽  
Graham C. Parker ◽  
William D. Lyman

2012 ◽  
Vol 32 (suppl_1) ◽  
Author(s):  
S Marlene Grenon ◽  
Jesus Aguado-Zuniga ◽  
Michael Conte ◽  
Millie Hughes-Fulford

Objectives: Mechanical forces including gravity affect mechanotransduction and subsequent cell function. The goal of this study was to investigate the impact of mechanical unloading (MU) and loading (ML) of endothelial cells (ECs) with microgravity and hypergravity respectively, with the hypothesis that MU alters expression of inflammatory and adhesion molecule gene expression and these changes are reversed by ML. Methods: Human umbilical vascular endothelial cells (HUVECs) grown to confluency were studied. A desktop random positioning machine and a gravitational cell-loading apparatus provided MU and ML conditions, respectively. The experimental conditions included: 1) controls exposed to 1-gravity environment for 24 h (CL), 2) MU for 24 hours, 3) MU for 24 hours with three 30-minutes periods of ML of 12-gravity (MU/ML). Gene expression was studied with reverse transcription followed by real-time quantitative polymerase chain reaction (qRTPCR). Results: MU led to a significant decrease in gene expression of the adhesion molecules ICAM-1, VCAM-1, E-Selectin, as well as TNF-α, IL-6 and VEGF. In contrast, NOS-3, Caveolin-1 and -2 were significantly increased with MU. The changes observed in gene expression with MU were reversed by gravitational mechanical loading (MU/ML). Conclusions: Gravitational MU decreases inflammatory and adhesion molecule gene expression and these changes are reversed by short periods of ML. This points towards the importance of gravitational loading in ECs function and cellular interactions.


2002 ◽  
Vol 457 (2-3) ◽  
pp. 195-200 ◽  
Author(s):  
Ellen Schoof ◽  
Katharina von der Hardt ◽  
Michael A Kandler ◽  
Franziska Abendroth ◽  
Thomas Papadopoulos ◽  
...  

2018 ◽  
Vol 206 (1-2) ◽  
pp. 73-81 ◽  
Author(s):  
Xue Yin ◽  
Silvia  Gonzales ◽  
Somya Sha ◽  
Howard Levene ◽  
Chun-Yuh Huang

Compressive loading promotes adenosine triphosphate (ATP) production and release by intervertebral disc (IVD) cells. Extracellular ATP can be rapidly hydrolyzed by ectonucleotidases. Adenosine, one of the adenine derivatives of ATP hydrolysis, can modulate diverse cellular actions via adenosine receptors. The objectives of this study were to investigate the effects of exogenous adenosine on the production of extracellular matrix (ECM; i.e., collagen type II and aggrecan) and ATP of IVD cells and explore the underlying mechanism of action. It was found that adenosine treatment significantly upregulated aggrecan and type II collagen gene expression and the ATP level in IVD cells. Dipyridamole, an adenosine transport blocker, completely suppressed the effects of adenosine on the ATP production and ECM gene expression of the IVD cells, whereas antagonists of adenosine receptors did not significantly affect adenosine-treated IVD cells. The findings suggested that elevated intracellular ATP and upregulation of ECM gene expression by adenosine treatment are mainly due to adenosine uptake rather than receptor activation. Since ECM biosynthesis is a high ATP demanding process, supplementing adenosine could be beneficial as IVD cells are able to utilize it to replenish intracellular ATP and sequentially promote ECM production, which is constantly suppressed by limited nutrition supply due to the avascular nature of the IVD.


1998 ◽  
Vol 25 (1) ◽  
pp. 33-41 ◽  
Author(s):  
Mini Paulose ◽  
Brydon L Bennett ◽  
Anthony M Manning ◽  
Karim Essani

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