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

被引:16
作者
Chiariello, Antonio [1 ]
Valente, Sabrina [1 ]
Pasquinelli, Gianandrea [1 ]
Baracca, Alessandra [2 ]
Sgarbi, Gianluca [2 ]
Solaini, Giancarlo [2 ]
Medici, Valentina [3 ]
Fantini, Valentina [3 ]
Poloni, Tino Emanuele [3 ]
Tognocchi, Monica [4 ]
Arcaro, Marina [5 ]
Galimberti, Daniela [5 ]
Franceschi, Claudio [6 ]
Capri, Miriam [1 ,7 ]
Salvioli, Stefano [1 ,7 ]
Conte, Maria [1 ,7 ]
机构
[1] Univ Bologna, Dept Expt Diagnost & Specialty Med DIMES, Bologna, Italy
[2] Univ Bologna, Dept Biomed & Neuromotor Sci DIBINEM, Lab Biochem & Mitochondrial Pathophysiol, Bologna, Italy
[3] Golgi Cenci Fdn, Dept Neurol & Neuropathol, Milan, Italy
[4] Univ Pisa, Dept Agr Food & Environm, Pisa, Italy
[5] Fdn Ca Granda IRCCS Osped Maggiore Policlin, Milan, Italy
[6] Natl Res Lobachevsky State Univ Nizhny Novgorod, Dept Appl Math, Inst ITMM, Nizhnii Novgorod, Russia
[7] Univ Bologna, Interdept Ctr Alma Mater Res Inst Global Challenge, Bologna, Italy
关键词
GDF15; Alzheimer's disease; aging; inflammation; mitochondrial dysfunction; DIFFERENTIATION FACTOR 15; STRESS-RESPONSE; COGNITIVE IMPAIRMENT; RECEPTOR; MITOCHONDRIA; GDF-15; DEATH; BETA; P53; PATHOLOGY;
D O I
10.3389/fnagi.2022.1058665
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
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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页数:16
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