The journal of sexual medicine · 2013
Peyronie's disease and mechanotransduction: an in vitro analysis of the cellular changes to Peyronie's disease in a cell-culture strain system.
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Chung Eric, De Young Ling, Solomon Matthew, Brock Gerald B
Аннотация
INTRODUCTION: Penile traction therapy (PTT) has gained considerable popularity as a noninvasive treatment option in Peyronie's disease (PD) to improve penile curvature and length. However the exact mechanism of action of PTT is unknown and as yet unproven.
AIM: Using a cyclic strain culture system, we investigate the cellular changes to the tunical tissues following equibiaxial tractional forces. The observed protein alteration following mechanical traction should replicate the changes observed in tunical tissue following PTT.
METHODS: Flexcell FX-5000(TM) Tension Plus system (Flexcell International Corporation, McKee-sport, PA, USA) is a pressurized chamber system that allows for sustained and dynamic application of hydrostatic pressure to cellular culture. Primary cell cultures from PD and normal tunical tissue (control) were sub-cultured on BioFlex-ProNectin plate 1 × 106 (Flexcell International Corporation, Hillsborough, NC, USA) for 24 hours and exposed to Flexcell sinusoidal strain of 18% at 1 Hz (strained group) on the biaxial plates for 24 hours under 37 °C in a 5% CO2 atmosphere.
MAIN OUTCOMES MEASURES: Immunohistochemistry (IHC) stains and Western blot assays between strained and nonstrained (control) cells.
RESULTS: Significant increase in smooth muscle α-actin, β-catenin, and Hsp 47 proteins were measured in the PD group compared with control group. IHC staining revealed a decrease in α-actin staining while Western blot assay showed an increase in metalloproteinase-8 expression with no measured change in β-catenin level in the strained PD group.
CONCLUSIONS: This novel study of cells derived from diseased and normal human tunica albuginea cultured in a mechanical strained environment provides good scientific evidence for the use of penile traction device in Peyronie's plaque remodeling.
AIM: Using a cyclic strain culture system, we investigate the cellular changes to the tunical tissues following equibiaxial tractional forces. The observed protein alteration following mechanical traction should replicate the changes observed in tunical tissue following PTT.
METHODS: Flexcell FX-5000(TM) Tension Plus system (Flexcell International Corporation, McKee-sport, PA, USA) is a pressurized chamber system that allows for sustained and dynamic application of hydrostatic pressure to cellular culture. Primary cell cultures from PD and normal tunical tissue (control) were sub-cultured on BioFlex-ProNectin plate 1 × 106 (Flexcell International Corporation, Hillsborough, NC, USA) for 24 hours and exposed to Flexcell sinusoidal strain of 18% at 1 Hz (strained group) on the biaxial plates for 24 hours under 37 °C in a 5% CO2 atmosphere.
MAIN OUTCOMES MEASURES: Immunohistochemistry (IHC) stains and Western blot assays between strained and nonstrained (control) cells.
RESULTS: Significant increase in smooth muscle α-actin, β-catenin, and Hsp 47 proteins were measured in the PD group compared with control group. IHC staining revealed a decrease in α-actin staining while Western blot assay showed an increase in metalloproteinase-8 expression with no measured change in β-catenin level in the strained PD group.
CONCLUSIONS: This novel study of cells derived from diseased and normal human tunica albuginea cultured in a mechanical strained environment provides good scientific evidence for the use of penile traction device in Peyronie's plaque remodeling.