Dipeptidyl-Peptidase IV Activity Is Correlated with Colorectal Cancer Prognosis

Background Dipeptidyl-peptidase IV (EC 3.4.14.5) (DPPIV) is a serine peptidase involved in cell differentiation, adhesion, immune modulation and apoptosis, functions that control neoplastic transformation. Previous studies have demonstrated altered expression and activity of tissue and circulating DPPIV in several cancers and proposed its potential usefulness for early diagnosis in colorectal cancer (CRC). Methods and principal findings The activity and mRNA and protein expression of DPPIV was prospectively analyzed in adenocarcinomas, adenomas, uninvolved colorectal mucosa and plasma from 116 CRC patients by fluorimetric, quantitative RT-PCR and immunohistochemical methods. Results were correlated with the most important classic pathological data related to aggressiveness and with 5-year survival rates. Results showed that: 1) mRNA levels and activity of DPPIV increased in colorectal neoplasms (Kruskal-Wallis test, p<0.01); 2) Both adenomas and CRCs displayed positive cytoplasmic immunostaining with luminal membrane reinforcement; 3) Plasmatic DPPIV activity was lower in CRC patients than in healthy subjects (Mann-U test, p<0.01); 4) Plasmatic DPPIV activity was associated with worse overall and disease-free survivals (log-rank p<0.01, Cox analysis p<0.01). Conclusion/significance 1) Up-regulation of DPPIV in colorectal tumors suggests a role for this enzyme in the neoplastic transformation of colorectal tissues. This finding opens the possibility for new therapeutic targets in these patients. 2) Plasmatic DPPIV is an independent prognostic factor in survival of CRC patients. The determination of DPPIV activity levels in the plasma may be a safe, minimally invasive and inexpensive way to define the aggressiveness of CRC in daily practice.

Pharmacological Blockade of Cannabinoid CB1 Receptors in Diet-Induced Obesity Regulates Mitochondrial Dihydrolipoamide Dehydrogenase in Muscle

Cannabinoid CB1 receptors peripherally modulate energy metabolism. Here, we investigated the role of CB1 receptors in the expression of glucose/pyruvate/tricarboxylic acid (TCA) metabolism in rat abdominal muscle. Dihydrolipoamide dehydrogenase (DLD), a flavoprotein component (E3) of alpha-ketoacid dehydrogenase complexes with diaphorase activity in mitochondria, was specifically analyzed. After assessing the effectiveness of the CB1 receptor antagonist AM251 (3 mg kg(-1), 14 days) on food intake and body weight, we could identified seven key enzymes from either glycolytic pathway or TCA cycle-regulated by both diet and CB1 receptor activity-through comprehensive proteomic approaches involving two-dimensional electrophoresis and MALDI-TOF/LC-ESI trap mass spectrometry. These enzymes were glucose 6-phosphate isomerase (GPI), triosephosphate isomerase (TPI), enolase (Eno3), lactate dehydrogenase (LDHa), glyoxalase-1 (Glo1) and the mitochondrial DLD, whose expressions were modified by AM251 in hypercaloric diet-induced obesity. Specifically, AM251 blocked high-carbohydrate diet (HCD)-induced expression of GPI, TPI, Eno3 and LDHa, suggesting a down-regulation of glucose/pyruvate/lactate pathways under glucose availability. AM251 reversed the HCD-inhibited expression of Glo1 and DLD in the muscle, and the DLD and CB1 receptor expression in the mitochondrial fraction. Interestingly, we identified the presence of CB1 receptors at the membrane of striate muscle mitochondria. DLD over-expression was confirmed in muscle of CB1-/- mice. AM251 increased the pyruvate dehydrogenase and glutathione reductase activity in C2C12 myotubes, and the diaphorase/oxidative activity in the mitochondria fraction. These results indicated an up-regulation of methylglyoxal and TCA cycle activity. Findings suggest that CB1 receptors in muscle modulate glucose/pyruvate/lactate pathways and mitochondrial oxidative activity by targeting DLD.

Diferenças intra e interespecíficas na atividade da fosfatase alcalina em microalgas marinhas costeiras selecionadas

A incorporação de fósforo (P) foi avaliada através da técnica de marcador enzimático fluorescente a fim de determinar a atividade da fosfatase alcalina (PA) em dois clones de Phaeodactylum tricornutum (Bohlin), Ub3 e Ub7, isolados de Ubatuba (SP), em Tetraselmis aff. chui (Butcher) e Prorocentrum minimum (Pavillard) J. Schiller, isoladas da Baía de Guanabara (RJ) e na Comunidade Natural da Baía de Guanabara (RJ). A fosfatase alcalina (PA) é uma enzima extracelular associada à membrana que catalisa a hidrólise de compostos orgânicos de fósforo em resposta à limitação de fosfato. Sua análise, a partir do marcador ELF-97, proporciona uma avaliação individual e, portanto, determina as condições nutricionais de fósforo inorgânico em células fitoplanctônicas. Os clones de P. tricornutum apresentaram diferenças no desenvolvimento quando incubados no tratamento P-repleto. O clone Ub7 de P. tricornutum apresentou a maior atividade enzimática quando comparado às demais espécies testadas, em condições P-repletas. Enquanto P. minimum apresentou a maior atividade da fosfatase alcalina em condições P-limitadas. Entre as espécies T. aff. chui e P. minimum, a maior atividade enzimática ocorreu durante a fase estacionária de desenvolvimento, entretanto diferenças foram observadas somente nas menores concentrações de fosfato. P. tricornutum, T. aff. chui e P. minimum, ao longo dos experimentos, utilizaram duas estratégias para incorporação de fosfato, aumentando a atividade da fosfatase alcalina, assim como alterando o biovolume ou a máxima dimensão linear para manter a relação S/V estável. Em P. tricornutum os sítios da atividade enzimática ocorreram na membrana celular, em T. aff. chui encontrados intracelularmente, enquanto em P. minimum observados tanto nas membranas, quanto no interior das células. No experimento realizado com a comunidade natural, houve predomínio das diatomáceas entre todos os grupos e tratamentos; as espécies foram agrupadas nas estratégias adaptativas C e R e classificadas principalmente como R-estrategistas. Os dinoflagelados da Ordem Prorocentrales utilizaram a incorporação do fósforo orgânico como estratégia para obtenção de fósforo em condições limitantes. Entretanto, as diatomáceas apresentaram tal estratégia de forma mais variável. Quanto às prasinofíceas, embora Tetraselmis sp. tenha apresentado baixa atividade enzimática nos experimentos unialgais, as concentrações de fosfato ao longo do experimento não resultaram na utilização de P orgânico para o grupo. Os resultados destacaram as diferenças intra e interespecíficas na atividade da fosfatase alcalina, e, consequentemente, na incorporação de fósforo orgânico, uma vez que as espécies testadas regularam a atividade enzimática de acordo com as diferentes concentrações externas de fosfato.

Synapses with short-term plasticity are optimal estimators of presynaptic membrane potentials.

The trajectory of the somatic membrane potential of a cortical neuron exactly reflects the computations performed on its afferent inputs. However, the spikes of such a neuron are a very low-dimensional and discrete projection of this continually evolving signal. We explored the possibility that the neuron's efferent synapses perform the critical computational step of estimating the membrane potential trajectory from the spikes. We found that short-term changes in synaptic efficacy can be interpreted as implementing an optimal estimator of this trajectory. Short-term depression arose when presynaptic spiking was sufficiently intense as to reduce the uncertainty associated with the estimate; short-term facilitation reflected structural features of the statistics of the presynaptic neuron such as up and down states. Our analysis provides a unifying account of a powerful, but puzzling, form of plasticity.