Resveratrol Treatment in Human Parkin -Mutant Fibroblasts Modulates cAMP and Calcium Homeostasis Regulating the Expression of Mitochondria-Associated Membranes Resident Proteins

Parkin plays an important role in ensuring efficient mitochondrial function and calcium homeostasis. -mutant human fibroblasts, with defective oxidative phosphorylation activity, showed high basal cAMP level likely ascribed to increased activity/expression of soluble adenylyl cyclase and/or low expr...

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Veröffentlicht in:Biomolecules (Basel, Switzerland) Switzerland), 2021-10, Vol.11 (10), p.1511
Hauptverfasser: Signorile, Anna, Ferretta, Anna, Pacelli, Consiglia, Capitanio, Nazzareno, Tanzarella, Paola, Matrella, Maria Laura, Valletti, Alessio, De Rasmo, Domenico, Cocco, Tiziana
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Sprache:eng
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Zusammenfassung:Parkin plays an important role in ensuring efficient mitochondrial function and calcium homeostasis. -mutant human fibroblasts, with defective oxidative phosphorylation activity, showed high basal cAMP level likely ascribed to increased activity/expression of soluble adenylyl cyclase and/or low expression/activity of the phosphodiesterase isoform 4 and to a higher Ca level. Overall, these findings support the existence, in -mutant fibroblasts, of an abnormal Ca and cAMP homeostasis in mitochondria. In our previous studies resveratrol treatment of -mutant fibroblasts induced a partial rescue of mitochondrial functions associated with stimulation of the AMPK/SIRT1/PGC-1α pathway. In this study we provide additional evidence of the potential beneficial effects of resveratrol inducing an increase in the pre-existing high Ca level and remodulation of the cAMP homeostasis in -mutant fibroblasts. Consistently, we report in these fibroblasts higher expression of proteins implicated in the tethering of ER and mitochondrial contact sites along with their renormalization after resveratrol treatment. On this basis we hypothesize that resveratrol-mediated enhancement of the Ca level, fine-tuned by the ER-mitochondria Ca crosstalk, might modulate the pAMPK/AMPK pathway in -mutant fibroblasts.
ISSN:2218-273X
2218-273X
DOI:10.3390/biom11101511