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Shear stress increases endothelial platelet-derived growth factor mRNA levels
H J Hsieh1, N Q Li, J A Frangos
1Department of Chemical Engineering, Pennsylvania State University, University Park 16802.
The American Journal of Physiology
|February 1, 1991
Summary
Physiological shear stress significantly increases platelet-derived growth factor (PDGF) A and B chain mRNA in endothelial cells. This suggests a role for PDGF in blood vessel adaptation to blood flow.
Area of Science:
- Cardiovascular Biology
- Endothelial Cell Biology
- Molecular Biology
Background:
- Platelet-derived growth factor (PDGF) is a potent mitogen and vasoconstrictor.
- Endothelial cells play a crucial role in regulating blood flow and vascular adaptation.
- The effect of shear stress on PDGF expression in endothelial cells is not fully understood.
Purpose of the Study:
- To investigate the impact of shear stress on platelet-derived growth factor (PDGF) A and B chain mRNA levels in human umbilical vein endothelial cells (hUVEC).
Main Methods:
- Cultured hUVEC were exposed to varying levels of physiological shear stress (0-51 dyn/cm2).
- Platelet-derived growth factor (PDGF) A and B chain mRNA levels were quantified using quantitative analysis at different time points after shear stress onset.
Main Results:
- Physiological shear stress (16 dyn/cm2) significantly elevated both PDGF A and B mRNA levels in hUVEC, peaking at 1.5-2 hours.
- PDGF A mRNA showed a >10-fold increase, while PDGF B mRNA showed a 2-3 fold increase (P < 0.05).
- PDGF A mRNA levels increased with shear stress up to 6 dyn/cm2 and plateaued thereafter, while PDGF B mRNA levels exhibited a more complex, non-monotonic response to increasing shear stress.
Conclusions:
- Shear stress significantly upregulates PDGF A and B mRNA expression in endothelial cells.
- The findings suggest that shear stress-induced PDGF production by endothelial cells may contribute to the adaptation of blood vessels to blood flow.
- PDGF released from the endothelium may play a role in regulating blood flow in vivo.