Frontiers in Aging Neuroscience (Jan 2023)

The expression pattern of GDF15 in human brain changes during aging and in Alzheimer’s disease

  • Antonio Chiariello,
  • Sabrina Valente,
  • Gianandrea Pasquinelli,
  • Alessandra Baracca,
  • Gianluca Sgarbi,
  • Giancarlo Solaini,
  • Valentina Medici,
  • Valentina Fantini,
  • Tino Emanuele Poloni,
  • Monica Tognocchi,
  • Marina Arcaro,
  • Daniela Galimberti,
  • Claudio Franceschi,
  • Miriam Capri,
  • Miriam Capri,
  • Stefano Salvioli,
  • Stefano Salvioli,
  • Maria Conte,
  • Maria Conte

DOI
https://doi.org/10.3389/fnagi.2022.1058665
Journal volume & issue
Vol. 14

Abstract

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IntroductionGrowth Differentiation Factor 15 (GDF15) is a mitochondrial-stress-responsive molecule whose expression strongly increases with aging and age-related diseases. However, its role in neurodegenerative diseases, including Alzheimer’s disease (AD), is still debated.MethodsWe have characterized the expression of GDF15 in brain samples from AD patients and non-demented subjects (controls) of different ages.ResultsAlthough no difference in CSF levels of GDF15 was found between AD patients and controls, GDF15 was expressed in different brain areas and seems to be predominantly localized in neurons. The ratio between its mature and precursor form was higher in the frontal cortex of AD patients compared to age-matched controls (p < 0.05). Moreover, this ratio was even higher for centenarians (p < 0.01), indicating that aging also affects GDF15 expression and maturation. A lower expression of OXPHOS complexes I, III, and V in AD patients compared to controls was also noticed, and a positive correlation between GDF15 and IL-6 mRNA levels was observed. Finally, when GDF15 was silenced in vitro in dermal fibroblasts, a decrease in OXPHOS complexes transcript levels and an increase in IL-6 levels were observed.DiscussionAlthough GDF15 seems not to be a reliable CSF marker for AD, it is highly expressed in aging and AD brains, likely as a part of stress response aimed at counteracting mitochondrial dysfunction and neuroinflammation.

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