Dataset Information

TrkB Isoforms Differentially Affect AICD Production through Their Intracellular Functional Domains.

ABSTRACT: We report that NTRK2, the gene encoding for the TrkB receptor, can regulate APP metabolism, specifically AICD levels. Using the human neuroblastoma cell line SH-SY5Y, we characterized the effect of three TrkB isoforms (FL, SHC, T) on APP metabolism by knockdown and overexpression. We found that TrkB FL increases AICD-mediated transcription and APP levels while it decreases sAPP levels. These effects were mainly mediated by the tyrosine kinase activity of the receptor and partially by the PLC-?- and SHC-binding sites. The TrkB T truncated isoform did not have significant effects on APP metabolism when transfected by itself, while the TrkB SHC decreased AICD-mediated transcription. TrkB T abolished TrkB FL effects on APP metabolism when cotransfected with it while TrkB SHC cotransfected with TrkB FL still showed increased APP levels. In conclusion, we demonstrated that TrkB isoforms have differential effects on APP metabolism.

SUBMITTER: Ansaloni S

PROVIDER: S-EPMC3056454 | biostudies-literature | 2011 Feb

REPOSITORIES: biostudies-literature

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TrkB Isoforms Differentially Affect AICD Production through Their Intracellular Functional Domains.

Ansaloni Sara S Leung Brian P BP Sebastian Neeraj P NP Samudralwar Rohini R Gadaleta Mariana M Saunders Aleister J AJ

International journal of Alzheimer's disease 20110224

We report that NTRK2, the gene encoding for the TrkB receptor, can regulate APP metabolism, specifically AICD levels. Using the human neuroblastoma cell line SH-SY5Y, we characterized the effect of three TrkB isoforms (FL, SHC, T) on APP metabolism by knockdown and overexpression. We found that TrkB FL increases AICD-mediated transcription and APP levels while it decreases sAPP levels. These effects were mainly mediated by the tyrosine kinase activity of the receptor and partially by the PLC-γ- ...[more]

PMID: 21423675

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Project description:Gut-derived short-chain fatty acids (SCFA), formed by microbial fermentation of dietary fibers, are believed to be involved in the etiology of obesity and diabetes. Previous data from our group showed that colonic infusions of physiologically relevant SCFA mixtures attenuated whole-body lipolysis in overweight men. To further study potential mechanisms involved in the antilipolytic properties of SCFA, we aimed to investigate the in vitro effects of SCFA incubations on intracellular lipolysis and signaling using a human white adipocyte model, the human multipotent adipose tissue-derived stem (hMADS) cells.hMADS adipocytes were incubated with mixtures of acetate, propionate, and butyrate or single SCFA (acetate, propionate and butyrate) in concentrations ranging between 1?µmol/L and 1?mmol/L. Glycerol release and lipase activation was investigated during basal conditions and following ?-adrenergic stimulation.SCFA mixtures high in acetate and propionate decreased basal glycerol release, when compared to control (P?<?0.05), while mixtures high in butyrate had no effect. Also, ?-adrenergic receptor mediated glycerol release was not significantly altered following incubation with SCFA mixtures. Incubation with only acetate decreased basal (1?µmol/L) and ?-adrenergically (1?µmol/L and 1?mmol/L) mediated glycerol release when compared with control (P?<?0.05). In contrast, butyrate (1?µmol/L) slightly increased basal and ?-adrenergically mediated glycerol release compared with control (P?<?0.05), while propionate had no effect on lipolysis. The antilipolytic effect of acetate was accompanied by a reduced phosphorylation of hormone-sensitive lipase (HSL) at serine residue 650. In addition, inhibition of Gi G proteins following pertussis toxin treatment prevented the antilipolytic effect of acetate.The present data demonstrated that acetate was mainly responsible for the antilipolytic effects of SCFA and acts via attenuation of HSL phosphorylation in a Gi-coupled manner in hMADS adipocytes. Therefore, the modulation of colonic and circulating acetate may be an important target to modulate human adipose tissue lipid metabolism.

Dataset Information

TrkB Isoforms Differentially Affect AICD Production through Their Intracellular Functional Domains.

Publications

TrkB Isoforms Differentially Affect AICD Production through Their Intracellular Functional Domains.

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