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Carlos Gomez

Publications and source records attributed to Carlos Gomez.

4 recordsLinked to original sources
PubMed2004

Perilipin A mediates the reversible binding of CGI-58 to lipid droplets in 3T3-L1 adipocytes.

Perilipins, the major structural proteins coating the surfaces of mature lipid droplets of adipocytes, play an important role in the regulation of triacylglycerol storage and hydrolysis. We have used proteomic analysis to identify CGI-58, a member of the alpha/beta-hydrolase fold family of enzymes, as a component of lipid droplets of 3T3-L1 adipocytes. CGI-58 mRNA is highly expressed in adipose tissue and testes, tissues that also express perilipins, and at lower levels in liver, skin, kidney, and heart. Both endogenous CGI-58 and an ectopic CGI-58-GFP chimera show diffuse cytoplasmic localization in 3T3-L1 preadipocytes, but localize almost exclusively to the surfaces of lipid droplets in differentiated 3T3-L1 adipocytes. The localization of endogenous CGI-58 was investigated in 3T3-L1 cells stably expressing mutated forms of perilipin using microscopy. CGI-58 binds to lipid droplets coated with perilipin A or mutated forms of perilipin with an intact C-terminal sequence from amino acid 382 to 429, but not to lipid droplets coated with perilipin B or mutated perilipin A lacking this sequence. Immunoprecipitation studies confirmed these findings, but also showed co-precipitation of perilipin B and CGI-58. Remarkably, activation of cAMP-dependent protein kinase by the incubation of 3T3-L1 adipocytes with isoproterenol and isobutylmethylxanthine disperses CGI-58 from the surfaces of lipid droplets to a cytoplasmic distribution. This shift in subcellular localization can be reversed by the addition of propanolol to the culture medium. Thus, CGI-58 binds to perilipin A-coated lipid droplets in a manner that is dependent upon the metabolic status of the adipocyte and the activity of cAMP-dependent protein kinase.

1-Acylglycerol-3-Phosphate O-Acyltransferase↗
PubMed2004

Tubby proteins: the plot thickens.

The tubby mouse, which shows late-onset obesity and neurosensory deficits, arises from a mutation in the Tub gene. Tub shares homology with the genes for tubby-like proteins Tulp1, Tulp2 and Tulp3. Ablation of Tub, Tulp1 or Tulp3 causes disease phenotypes that are indicative of their importance in nervous-system function and development. Despite this importance, the biochemical functions of tubby-like proteins are only now beginning to be understood. At present, data indicate that tubby-like proteins might function as heterotrimeric-G-protein-responsive intracellular signalling factors, although an array of data also implicates them in other processes.

Adaptor Proteins, Signal Transducing↗
PubMed2003

Effects of temporal encoding on auditory object formation: a mismatch negativity study.

Analysis of auditory scene relies on the appropriate division of the sensory input into meaningful events. The auditory system uses a sequential grouping strategy to segregate different acoustic events in the time domain. As a result of grouping, the organization of sound is expected to include acoustic events spanning different scales of time. It is unclear, however, at which moment the central auditory system begins to introduce changes in the neural representation of the auditory scene as a result of grouping different information units into a larger acoustic event. The present set of experiments examines this issue by using the mismatch negativity (MMN) component of event-related potentials. The MMN is elicited in response to changes in the previously registered auditory regularity whether or not the subject's attention is focused on the auditory stimuli. By presenting three consecutive pairs of alternating tones in serial stimulus trains, we found that across-train repetitions of the tone elicited the MMN with inter-train intervals up to 240 ms. Beyond this interval, only within-train repetitions of the tone elicited the MMN, suggesting that pairs of tones were bound together into a single acoustic event (i.e., train of six tones) within a temporal window not much longer than 240 ms. Furthermore, a different pattern of responses was seen depending on the position of the deviant event within the train and the frequency distance between the alternating tones. These results suggest that grouping discrete auditory inputs may introduce changes in the neural representation of the auditory scene by applying rules to sounds spanning larger temporal scales.

Acoustic Stimulation↗