P62/SQSTM1 indirectly mediates remote multipotent mesenchymal cells and rescues bone loss and bone marrow integrity in ovariectomized rats. Issue 2 (24th December 2022)

• Record Type: Journal Article
• Authors: Agas, Dimitrios; Marchegiani, Andrea; Laus, Fulvio; Gabai, Vladimir; Sufianov, Albert A.; Shneider, Alexander; Sabbieti, Maria Giovanna
• Is Part Of: Journal of cellular physiology. Volume 238:Issue 2(2023)
• Page Start: 407
• Page End: 419
• Publication Date: 2022-12-24
• Subjects: bone physiology -- DNA plasmid -- multipotent mesenchymal cells -- osteoporosis -- p62; Physiology -- Periodicals; Cell physiology -- Periodicals; 571.6
• DOI: 10.1002/jcp.30937
• Languages: English
• ISSNs: 0021-9541

Abstract

Abstract: Intramuscular administration of p62/SQSTM1 (sequestosome1)‐encoding plasmid demonstrated an anticancer effect in rodent models and dogs as well as a high safety profile and the first evidence of clinical benefits in humans. Also, an anti‐inflammatory effect of the plasmid was reported in several rodent disease models. Yet, the mechanisms of action for the p62 plasmid remain unknown. Here, we tested a hypothesis that the p62‐plasmid can act through the modulation of bone marrow multipotent mesenchymal cells (MSCs). We demonstrated that a p62 plasmid can affect MSCs indirectly by stimulating p62‐transfected cells to secrete an active ingredient(s) sensed by untransfected MSCs. When we transfected MSCs with the p62‐plasmid, collected their supernatant, and added it to an untransfected MSCs culture, it switched the differentiation state and prompt osteogenic responses of the untransfected MSCs. According to an accepted viewpoint, ovariectomy leads to bone pathology via dysregulation of MSCs, and restoring the MSC homeostasis would restore ovariectomy‐induced bone damage. To validate our in vitro observations in a clinically relevant in vivo model, we administered the p62 plasmid to ovariectomized rats. It partially reversed bone loss and notably reduced adipogenesis with concurrent reestablishing of the MSC subpopulation pool within the bone marrow. Overall, our study suggests that remote modulation of progenitor MSCs via administering a p62‐encoding plasmid may constitute a mechanism for its previously reported effects and presents a feasible disease‐preventing and/or therapeutic strategy.