Peroxisomicine A1, a potential antineoplastic agent, causes micropexophagy in addition to macropexophagy.

Abstract

Peroxisomicine A1 (PA1) is a potential antineoplastic agent with high and selective toxicity toward peroxisomes of tumor cells. Pexophagy is a selective autophagy process that degrades damaged peroxisomes; this process has been studied mainly in methylotrophic yeasts. There are two main modes of pexophagy in yeast: macropexophagy and micropexophagy. Previous studies showed that peroxisomes damaged by a prolonged exposition to PA1 are eliminated by macropexophagy. In this work, Candida boidinii was grown in methanol-containing media, and PA1 was added to the cultures at 2 µg/mL after they reached the mid-exponential growth phase. Samples were taken at 5, 10, 15, 20, and 25 min after the addition of PA1 and processed for ultrastructural analysis. Typical morphological characteristics of micropexophagy were observed: the direct engulfment of peroxisomes by the vacuolar membrane and the presence of the micropexophagic membrane apparatus (MIPA), which mediates the fusion between the opposing tips of the vacuole to complete sequestration of peroxisomes from the cytosol. In conclusion, here we report that, in addition to macropexophagy, peroxisomes damaged by PA1 can be eliminated by micropexophagy. This information is useful to deepen the knowledge of the mechanism of action of PA1 and of that of pexophagy per se.

• Authors: Marta Ortega-Martínez, Vanessa Gutiérrez-Dávila, Alberto Niderhauser-García, Ricardo Salazar-Aranda, Juan M Solís-Soto, Roberto Montes-de-Oca-Luna, Gilberto Jaramillo-Rangel
• Journal: Cell biology international (Cell Biol Int) Vol. 44 Issue 3 Pg. 918-923 (Mar 2020) ISSN: 1095-8355 [Electronic] England
• PMID: 31814220 (Publication Type: Journal Article)
• Copyright: © 2019 International Federation for Cell Biology.

Chemical References

• Anthracenes
• Antineoplastic Agents
• Fungal Proteins
• Karwinskia toxin T-514

Topics

• Anthracenes (pharmacology)
• Antineoplastic Agents (pharmacology)
• Candida (drug effects)
• Fungal Proteins (metabolism)
• Macroautophagy (drug effects)
• Microautophagy (drug effects)
• Peroxisomes (drug effects)