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MINI REVIEW article Volume 14 - 2026 | doi: 10.3389/fcell.2026.1922536 Reviewed by MINI REVIEW article Article metrics View details Abstract In tissue development and regeneration, cellular behavior has traditionally been interpreted through biochemical signaling frameworks.
Abstract Iron overload (IO) induces insulin resistance in H9c2 cardiomyoblast cells. Here, we used H9c2 cells overexpressing MitoNEET to examine the potential for protection against iron accumulation in the mitochondria and subsequent insulin resistance. In control H9c2 cells, IO was observed to increase mitochondrial iron content, reactive oxygen species (ROS) production, mitochondrial fission, and reduced insulin-stimulated Akt and ERK1/2 phosphorylation.
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