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Liposomal inhibition of acrolein-induced injury in rat cultured urothelial cells
Authors:J. Nirmal  A. S. Wolf-Johnston  M. B. Chancellor  P. Tyagi  M. Anthony  J. Kaufman  L. A. Birder
Affiliation:1. Department of Urology, Oakland University William Beaumont School of Medicine, Rochester, MI, USA
2. Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA
3. Department of Urology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA
5. Lipella Pharmaceuticals Inc., Pittsburgh, PA, USA
4. Departments of Medicine and Pharmacology & Chemical Biology, University of Pittsburgh School of Medicine, A 1217 Scaife Hall, 3550 Terrace Street, Pittsburgh, PA, USA
Abstract:

Purpose

To study the protection offered by empty liposomes (LPs) alone against acrolein-induced changes in urothelial cell viability and explored uptake of LPs by primary (rat) urothelial cells.

Methods

Acrolein was used as a means to induce cellular damage and reduce urothelial cellular viability. The effect of acrolein or liposomal treatment on cellular proliferation was studied using 5-bromo-2′-deoxy-uridine assay. Cytokine release was measured after urothelial cells were exposed to acrolein. Temperature-dependent uptake study was carried out for fluorescent-labeled LPs using confocal microscopy.

Results

Liposome pretreatment protected against acrolein-induced decrease in urothelial cell proliferation. LPs also significantly affected the acrolein-induced cytokine (interferon-gamma) release offering protection to the urothelial cells against acrolein damage. We also observed a temperature-dependent urothelial uptake of fluorescent-labeled LPs occurred at 37 °C (but not at 4 °C).

Conclusions

Empty LPs alone provide a therapeutic efficacy against acrolein-induced changes in urothelial cell viability and may be a promising local therapy for bladder diseases. Hence, our preliminary evidence provides support for liposome-therapy for urothelial protection and possible repair.
Keywords:
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