Sulforaphane modifies mitochondrial-endoplasmic reticulum associations through reductive stress in cardiomyocytes

Mitochondria-endoplasmic reticulum (ER) communication relies on platforms formed at the ER membrane with the mitochondrial outer membrane contact sites (MERCs). MERCs are involved in several processes including the unfolded protein response (UPR) and calcium (Ca2+) signaling. Therefore, as alterations in MERCs greatly impact cellular metabolism, pharmacological interventions to preserve productive mitochondrial-ER communication have been explored to maintain cellular homeostasis. In this regard, extensive information has documented the beneficial and potential effects of sulforaphane (SFN) in different pathological conditions; however, controversy has arisen regarding the effect of this compound on mitochondria-ER interaction. Therefore, in this study, we investigated whether SFN could induce changes in MERCs under normal culture conditions without damaging stimuli. Our results indicate that non-cytotoxic concentration of 2.5 & mu;M SFN increased ER stress in cardiomyocytes in conjunction with a reductive stress environment, that diminishes ER-mitochondria association. Additionally, reductive stress promotes Ca2+ accumulation in the ER of cardiomyocytes. These data show an unexpected effect of SFN on cardiomyocytes grown under standard culture conditions, promoted by the cellular redox unbalance. Therefore, it is necessary to rationalize the use of compounds with antioxidant properties to avoid triggering cellular side effects.

Automated summary

Mitochondria-endoplasmic reticulum (ER) communication is dependent on platforms formed at the ER membrane with the mitochondrial outer membrane contact sites (MERCs). Alterations in MERCs greatly impact cellular metabolism, making the preservation of productive mitochondrial-ER communication crucial for cellular homeostasis. This study investigates the effect of sulforaphane (SFN), which is known to have potential therapeutic effects, on MERCs under normal culture conditions.