Journal Article

Enteric Bacterial Metabolites Propionic and Butyric Acid Modulate Gene Expression, Including CREB-Dependent Catecholaminergic Neurotransmission, in PC12 Cells - Possible Relevance to Autism Spectrum Disorders

MacFabe, Derrick F., La Gamma, Edmund F., Nankova, Bistra B., Agarwal, Raj

2014

Overview

Alterations in gut microbiome composition have an emerging role in health and disease including brain function and behavior. Short chain fatty acids (SCFA) like propionic (PPA), and butyric acid (BA), which are present in diet and are fermentation products of many gastrointestinal bacteria, are showing increasing importance in host health, but also may be environmental contributors in neurodevelopmental disorders including autism spectrum disorders (ASD). Further to this we have shown SCFA administration to rodents over a variety of routes (intracerebroventricular, subcutaneous, intraperitoneal) or developmental time periods can elicit behavioral, electrophysiological, neuropathological and biochemical effects consistent with findings in ASD patients. SCFA are capable of altering host gene expression, partly due to their histone deacetylase inhibitor activity. We have previously shown BA can regulate tyrosine hydroxylase (TH) mRNA levels in a PC12 cell model. Since monoamine concentration is known to be elevated in the brain and blood of ASD patients and in many ASD animal models, we hypothesized that SCFA may directly influence brain monoaminergic pathways. When PC12 cells were transiently transfected with plasmids having a luciferase reporter gene under the control of the TH promoter, PPA was found to induce reporter gene activity over a wide concentration range. CREB transcription factor(s) was necessary for the transcriptional activation of TH gene by PPA. At lower concentrations PPA also caused accumulation of TH mRNA and protein, indicative of increased cell capacity to produce catecholamines. PPA and BA induced broad alterations in gene expression including neurotransmitter systems, neuronal cell adhesion molecules, inflammation, oxidative stress, lipid metabolism and mitochondrial function, all of which have been implicated in ASD. In conclusion, our data are consistent with a molecular mechanism through which gut related environmental signals such as increased levels of SCFA's can epigenetically modulate cell function further supporting their role as environmental contributors to ASD.

• Publisher: Public Library of Science,Public Library of Science (PLoS)
• Subject: Animal models / Animals / Antibiotics / Autism / Biology and Life Sciences / Biomarkers / Brain / Brain research / Butyric acid / Butyric Acid - metabolism / Catecholamines / Cell adhesion / Cell adhesion molecules / Child Development Disorders, Pervasive - microbiology / Children & youth / Cyclic AMP response element-binding protein / Cyclic AMP Response Element-Binding Protein - metabolism / Digestive system / Digestive tract / Disorders / Enterobacteriaceae - physiology / Fatty acids / Fermentation / Gastrointestinal tract / Gene expression / Gene Expression Regulation / Gene Regulatory Networks / Histone deacetylase / Host-Pathogen Interactions / Hydroxylase / Intestinal microflora / Lipid metabolism / Metabolism / Metabolites / Microbiomes / Microbiota / Microorganisms / Mitochondria / Nervous system / Neurodevelopmental disorders / Neurosciences / Neurotransmission / Oxidative metabolism / Oxidative stress / Patients / PC12 Cells - metabolism / PC12 Cells - microbiology / Pediatrics / Pheochromocytoma cells / Physiology / Plasmids / Propionates - metabolism / Psychiatry / Rats / Reporter gene / Rodents / Synaptic Transmission / Systematic review / Transcription activation / Transcriptional Activation / Tyrosine / Tyrosine 3-Monooxygenase - genetics