Electron Microscopy in Rat Brain Slices Reveals Rapid Accumulation of Cisplatin on Ribosomes and Other Cellular Components Only in Glia

Author:

Zueva Lidia1,Rivera Yomarie2,Kucheryavykh Lilia3,Skatchkov Serguei N.23,Eaton Misty J.3,Sanabria Priscila2,Inyushin Mikhail2

Affiliation:

1. Department of Neuroscience, Universidad Central del Caribe, Bayamón, PR 00960, USA

2. Department of Physiology, Universidad Central del Caribe, Bayamón, PR 00960, USA

3. Department of Biochemistry, Universidad Central del Caribe, Bayamón, PR 00960, USA

Abstract

Cisplatin is a widely used, effective anticancer drug. Its use, however, is associated with several side effects including nephrotoxicity and neurotoxicity. It is known that cisplatin is accumulated in cells by the organic cation transport system and reacts with nucleotides, damaging them, but the precise target of cisplatin-induced neurotoxicity remains obscure. Here we report direct visualization of cisplatin inside brain cells using in vivo “cisplatin staining,” a technique that takes advantage of the high electron density of cisplatin, which contains platinum (atomic mass=195). After applying 0.1% cisplatin to living brain slices for 30 min, we fixed the tissue and observed the accumulated cisplatin using electron microscopy. We found that cisplatin was localized mainly to ribosomes associated with endoplasmic reticulum (EPR) in glial cells and to the myelin sheath formed by oligodendrocytes around neuronal axons. Staining of nuclear DNA was moderate. Our in vivo “cisplatin staining” method validated that the main target of cisplatin is a direct attack on myelin and the RNA contained in ribosomes.

Funder

National Institutes of Health

Publisher

Hindawi Limited

Subject

Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics,Oncology

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