Inhibition of PP2A Activity by HO During Mitosis Disrupts Nuclear Envelope Reassembly and Alters Nuclear Shape
Overview
Molecular Biology
Affiliations
Many types of cancer cells exhibit abnormal nuclear shapes induced by various molecular changes. However, whether reactive oxygen species (ROS) induce nuclear deformation has not been fully addressed. Here, we show that hydrogen peroxide (HO) treatment induced concentration-dependent alterations in nuclear shape that were abolished by pretreatment with the antioxidant N-acetyl-L-cysteine or by catalase overexpression. Interestingly, treatment with HO induced nuclear shape alterations significantly more frequently in mitotic cells than in asynchronous cells, suggesting that HO mainly affects nuclear envelope disassembly and/or reassembly processes. Because protein phosphatase 2 A (PP2A) activity is reported to be involved in nuclear envelope reassembly during mitosis, we investigated the possible involvement of PP2A. Indeed, HO reduced the activity of PP2A, an effect that was mimicked by the PP1 and PP2A inhibitor okadaic acid. Moreover, overexpression of PP2A but not PP1 or PP4 partially rescued HO-induced alterations in nuclear shape, indicating that the decrease in PP2A activity induced by HO is specifically involved in the observed nuclear shape alterations. We further show that treatment of mitotic cells with HO induced the mislocalization of BAF (barrier-to-autointegration factor), a substrate of PP2A, during telophase. This effect was associated with Lamin A/C mislocalization and was rescued by PP2A overexpression. Collectively, our findings suggest that HO preferentially affects mitotic cells through PP2A inhibition, which induces the subsequent mislocalization of BAF and Lamin A/C during nuclear envelope reassembly, leading to the formation of an abnormal nuclear shape.
Akt3 links mitochondrial function to the regulation of Aurora B and mitotic fidelity.
Hough Z, Nasehi F, Corum D, Norris R, Foley A, Muise-Helmericks R PLoS One. 2025; 20(3):e0315751.
PMID: 40048438 PMC: 11884723. DOI: 10.1371/journal.pone.0315751.
Elzamzami F, Samal A, Arun A, Dharmaraj T, Prasad N, Rendon-Jonguitud A Front Cell Dev Biol. 2023; 11:1240285.
PMID: 37936983 PMC: 10626543. DOI: 10.3389/fcell.2023.1240285.
Nuclear envelope assembly relies on CHMP-7 in the absence of BAF-LEM-mediated hole closure.
Barger S, Penfield L, Bahmanyar S J Cell Sci. 2023; 136(21).
PMID: 37795681 PMC: 10668030. DOI: 10.1242/jcs.261385.
Nuclear envelope assembly relies on CHMP-7 in the absence of BAF-LEM-mediated hole closure.
Barger S, Penfield L, Bahmanyar S bioRxiv. 2023; .
PMID: 37461528 PMC: 10350047. DOI: 10.1101/2023.07.06.547980.
TSC22D4 interacts with Akt1 to regulate glucose metabolism.
Demir S, Wolff G, Wieder A, Maida A, Buhler L, Brune M Sci Adv. 2022; 8(42):eabo5555.
PMID: 36269831 PMC: 9586482. DOI: 10.1126/sciadv.abo5555.