Evidence map›Paper›PMID 37894823›Full record

ArticleInternational journal of molecular sciences2023

Mitochondrial sAC-cAMP-PKA Axis Modulates the ΔΨ

Rosella Scrima, Olga Cela, Michela Rosiello, Ari Qadir Nabi, Claudia Piccoli, Giuseppe Capitanio, Francesco Antonio Tucci, Aldo Leone, Giovanni Quarato, Nazzareno Capitanio

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Deciphering the language of mingling lipids and proteins.Current opinion in structural biology · 2025
    Review
  4. Article
  5. Special Issue "Mitochondrial Respiration in Physiology and Pathology".International journal of molecular sciences · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Rosella ScrimaDepartment of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.
Olga CelaDepartment of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.
Michela RosielloDepartment of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.
Ari Qadir NabiDepartment of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.ORCID 0000-0001-6844-1134
Claudia PiccoliDepartment of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.
Giuseppe CapitanioDepartment of Translational Biomedicine and Neuroscience, University of Bari "Aldo Moro", 70124 Bari, Italy.ORCID 0000-0002-9369-4608
Francesco Antonio TucciEuropean Institute of Oncology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 20141 Milan, Italy.ORCID 0000-0001-6247-5392
Aldo LeoneDepartment of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.
Giovanni QuaratoTreeline Biosciences, San Diego, CA 92121, USA.ORCID 0000-0003-1167-3422
Nazzareno CapitanioDepartment of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.ORCID 0000-0001-9285-051X

Funding

University of Foggia PRA-2022
6 · The paper itself

Abstract

The current view of the mitochondrial respiratory chain complexes I, III and IV foresees the occurrence of their assembly in supercomplexes, providing additional functional properties when compared with randomly colliding isolated complexes. According to the plasticity model, the two structural states of the respiratory chain may interconvert, influenced by the intracellular prevailing conditions. In previous studies, we suggested the mitochondrial membrane potential as a factor for controlling their dynamic balance. Here, we investigated if and how the cAMP/PKA-mediated signalling influences the aggregation state of the respiratory complexes. An analysis of the inhibitory titration profiles of the endogenous oxygen consumption rates in intact HepG2 cells with specific inhibitors of the respiratory complexes was performed to quantify, in the framework of the metabolic flux theory, the corresponding control coefficients. The attained results, pharmacologically inhibiting either PKA or sAC, indicated that the reversible phosphorylation of the respiratory chain complexes/supercomplexes influenced their assembly state in response to the membrane potential. This conclusion was supported by the scrutiny of the available structure of the CI/CIII

Indexed as

MitochondriaMitochondrial MembranesElectron TransportElectron Transport Complex IPhosphorylationElectron Transport Complex IcAMP/PKA signaling pathwaymetabolic flux theorymitochondrial membrane potentialmitochondrial respiratory chain complexessoluble adenylate cyclasesupercomplexes

Identifiers

PMID37894823
PMCPMC10607245

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.