Distribution of the p66Shc Adaptor Protein Among Mitochondrial and Mitochondria-Associated Membranes Fractions in Normal and Oxidative Stress Conditions

• Published in: International journal of molecular sciences 2024-12, Vol.25 (23), p.12835
• Main Authors: Lebiedzinska-Arciszewska, Magdalena, Pakula, Barbara, Bonora, Massimo, Missiroli, Sonia, Potes, Yaiza, Jakubek-Olszewska, Patrycja, Simoes, Ines C M, Pinton, Paolo, Wieckowski, Mariusz R
• Format: Article
• Language: English
• Subjects: Aging; Animals; Antigens; Apoptosis; Autophagy; Cell death; Communication; Cytochrome; Cytochrome c; Dehydrogenases; Endoplasmic reticulum; Hep G2 Cells; Homeostasis; Humans; Hydrogen Peroxide - metabolism; Ischemia; Kinases; Liver; Liver - metabolism; Liver cancer; Localization; Male; Membranes; Metabolism; Mice; Mitochondria; Mitochondria - metabolism; Mitochondria Associated Membranes; Mitochondrial Membranes - metabolism; Oxidative Stress; Peroxides; Phosphorylation; Proteins; Reactive oxygen species; Signal transduction; Src Homology 2 Domain-Containing, Transforming Protein 1 - genetics; Src Homology 2 Domain-Containing, Transforming Protein 1 - metabolism
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms252312835

p66Shc is an adaptor protein and one of the cellular fate regulators since it modulates mitogenic signaling pathways, mitochondrial function, and reactive oxygen species (ROS) production. p66Shc is localized mostly in the cytosol and endoplasmic reticulum (ER); however, under oxidative stress, p66Shc is post-translationally modified and relocates to mitochondria. p66Shc was found in the intermembrane space, where it interacts with cytochrome c, contributing to the hydrogen peroxide generation by the mitochondrial respiratory chain. Our previous studies suggested that p66Shc is localized also in mitochondria-associated membranes (MAM). MAM fraction consists of mitochondria and mostly ER membranes. Contact sites between ER and mitochondria host proteins involved in multiple processes including calcium homeostasis, apoptosis, and autophagy regulation. Thus, p66Shc in MAM could participate in processes related to cell fate determination. Due to reports on various and conditional p66Shc intracellular localization, in the present paper, we describe the allocation of p66Shc pools in different subcellular compartments in mouse liver tissue and HepG2 cell culture. We provide additional evidence for p66Shc localization in MAM. In the present study, we use precisely purified subcellular fraction isolated by differential centrifugation-based protocol from control mouse liver tissue and HepG2 cells and from cells treated with hydrogen peroxide to promote mitochondrial p66Shc translocation. We performed controlled digestion of crude mitochondrial fraction, in which the degradation patterns of p66Shc and MAM fraction marker proteins were comparable. Moreover, we assessed the distribution of the individual ShcA isoforms (p46Shc, p52Shc, and p66Shc) in the subcellular fractions and their contribution to the total ShcA in control mice livers and HepG2 cells. In conclusion, we showed that a substantial pool of p66Shc protein resides in MAM in control conditions and after oxidative stress induction.