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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Methylmalonic Acid Compromises Respiration and Reduces the Expression of Differentiation Markers of SH-SY5Y Human Neuroblastoma Cells

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Author(s):
da Costa, Renata T. [1] ; dos Santos, Marcella B. [1] ; Silva, Izabel C. S. [1] ; de Almeida, Raquel P. [1] ; Teruel, Marcela S. [1] ; Carrettiero, Daniel C. [1] ; Ribeiro, Cesar A. J. [1]
Total Authors: 7
Affiliation:
[1] Univ Fed ABC UFABC, Ctr Ciencias Nat & Humanas CCNH, BR-09606070 Sao Bernardo Do Campo, SP - Brazil
Total Affiliations: 1
Document type: Journal article
Source: ACS Chemical Neuroscience; v. 12, n. 14, p. 2608-2618, JUL 21 2021.
Web of Science Citations: 0
Abstract

Methylmalonic acidemia is a rare metabolic disorder caused by the deficient activity of L-methylmalonyl-CoA mutase or its cofactor 5-deoxyadenosylcobalamin and is characterized by accumulation of methylmalonic acid (MMA) and alternative metabolites. The brain is one of the most affected tissues and neurologic symptoms, characterized by seizures, mental retardation, psychomotor abnormalities, and coma, commonly appear in newborns. The molecular mechanisms of neuropathogenesis in methylmalonic acidemia are still poorly understood, specifically regarding the impairments in neuronal development, maturation, and differentiation. In this study, we investigated the effects of MMA in both undifferentiated and differentiated phenotypes of SH-SY5Y human neuroblastoma cells. We observed an increase in glucose consumption and reduction in respiratory parameters of both undifferentiated and differentiated cells after exposition to MMA, suggesting that differentiated cells are slightly more prone to perturbations in respiratory parameters by MMA than undifferentiated cells. Next, we performed qPCR of mature neuronal-specific gene markers and measured mitochondrial functioning to evaluate the role of MMA during differentiation. Our results showed that MMA impairs the respiratory parameters only at the late stage of differentiation and downregulates the transcriptional gene profile of mature neuronal markers neuron-specific enolase (ENO2) and synaptophysin (SYP). Altogether, our findings point out important changes observed during neuronal maturation and energetic stress vulnerability that can play a role in the neurological clinical symptoms at the newborn period and reveal important molecular mechanisms that could help the screening of targets to new approaches in the therapies of this disease. (AU)

FAPESP's process: 15/23426-9 - Beta-amyloid in Alzheimer's Disease: death or survival? Involvement of NF-kappaB and BAG2
Grantee:Daniel Carneiro Carrettiero
Support Opportunities: Regular Research Grants
FAPESP's process: 15/25541-0 - Investigation of the mechanisms of toxicity in methylmalonic academia - evaluation of cell bioenergetics, oxidative stress, signaling pathways and potential strategies of protection
Grantee:César Augusto João Ribeiro
Support Opportunities: Regular Research Grants