# Methamphetamine Increases Tubulo-Vesicular Areas While Dissipating Proteins from Vesicles Involved in Cell Clearance

## TL;DR

Methamphetamine disrupts cell cleanup structures, leading to a loss of compartmentalization and reduced cell function.

## Contribution

The study identifies specific organelle changes and protein dissipation in cells exposed to methamphetamine.

## Key findings

- METH increases autophagosomes and damaged mitochondria while decreasing lysosomes and healthy mitochondria.
- Proteins like LC3, p62, LAMP1, and Cathepsin-D are reduced within their respective vesicles after METH exposure.
- The findings suggest a loss of compartmentalization and reduced cell clearance competence during degeneration.

## Abstract

Cytopathology induced by methamphetamine (METH) is reminiscent of degenerative disorders such as Parkinson’s disease, and it is characterized by membrane organelles arranged in tubulo-vesicular structures. These areas, appearing as clusters of vesicles, have never been defined concerning the presence of specific organelles. Therefore, the present study aimed to identify the relative and absolute area of specific membrane-bound organelles following a moderate dose (100 µM) of METH administered to catecholamine-containing PC12 cells. Organelles and antigens were detected by immunofluorescence, and they were further quantified by plain electron microscopy and in situ stoichiometry. This analysis indicated an increase in autophagosomes and damaged mitochondria along with a decrease in lysosomes and healthy mitochondria. Following METH, a severe dissipation of hallmark proteins from their own vesicles was measured. In fact, the amounts of LC3 and p62 were reduced within autophagy vacuoles compared with the whole cytosol. Similarly, LAMP1 and Cathepsin-D within lysosomes were reduced. These findings suggest a loss of compartmentalization and confirm a decrease in the competence of cell clearing organelles during catecholamine degeneration. Such cell entropy is consistent with a loss of energy stores, which routinely govern appropriate subcellular compartmentalization.