Efectos del diálogo socrático sobre el pensamiento crítico en estudiantes universitarios

In this study –based on Richard Paul’s perspective- the general objective was to prove the effectiveness of the Socratic dialogue in relation to critical thinking in university students. To do this, a quasi-experimental design was selected, and techniques such as observation and discussion were used. Protocols, diaries, video recorder, TV, VHS, and a training handbook for Socratic dialogue were used as instruments. Results show that a total of 706 questions were asked. From them, the critical thinking subcategories “clarity” (68%) and “precision” (19%) are highlighted as a trend. The rest of the subcategories are: “accuracy” (0%), “relevance” (1%), “depth” (9%), “breadth” (0%) and “logic” (3%). It can be stated that the proposed objective was achieved because the findings show –based on the statistical process carried out through “Z”, “U” and “W” tests – that the students of the experimental group surpassed in a significant way to those of the control group in the subcategories “clarity” and “precision”, taking into account intra and inter group analyses: a) Total and specific frequencies of the Socratic questions asked by teachers, considered as “pre” and “post” conditions of the groups, and b) “Low”, “medium” and “high” scores in students’ critical thinking answers to teachers’ questions in such groups and conditions.En este estudio --siguiendo las perspectivas de Richard Paul-- se planteó como objetivo general probar la efectividad del diálogo socrático con relación al pensamiento crítico en un grupo de estudiantes universitarios. Para tal efecto se recurrió a un diseño cuasiexperimental, utilizando como técnicas la “observación” y la “discusión”. Como instrumento se aplicaron protocolos, cuadernos para registros en el aula, grabadora de vídeo, televisor, V.H.S. y un manual de entrenamiento en diálogo socrático. Los resultados indican que se formularon un total de 706 preguntas de las cuales se destacan las subcategorías de pensamiento crítico “claridad” (68%) y “precisión” (19%) como tendencia. El resto son: “exactitud” (0%), “pertinencia” (1%), “profundidad” (9%), “amplitud” (0%) y lógica (3%). Se puede afirmar que se cumplió con el objetivo propuesto, ya que los hallazgos en este estudio muestran —basados en el proceso estadístico llevado a cabo a través de las pruebas “Z”, “U” y “W”— que los estudiantes del grupo experimental superaron en forma significativa a los del grupo de control en las subcategorías “claridad” y “precisión”, considerando un análisis intra e intergrupales: a) Las frecuencias totales y específicas de las preguntas socráticas formuladas por los profesores, consideradas las condiciones “antes” y “después” de los grupos en mención y, b) las valoraciones “bajas”, “medias” y “altas” en las respuestas de pensamiento crítico de los alumnos en dichos grupos y condiciones

Identification of a highly polymorphic tetranucleotide repeat locus (DXpS) at Xp and development of a DXpS/HUMARA biplex methylation-based PCR assay that enhances detection of X-chromosome inactivation

The methylation-based PCR assay at the polymorphic (CAG)n repeat in exon 1 of the human androgen receptor _AR_ gene (HUMARA) is a standard method for determination of the methylation state of alleles in active X (Xa) and inactive X (Xi) chromosomes. HUMARA assay is endowed with heterozygosity rates ~85% worldwide. This means that in a proportion of females it is uninformative. The HUMARA genotype is not neutral, being linked to Kennedy´s disease. Moreover, allele designation and quantification from trinucleotide repeats demand normalizing for minor (stutter) products differing from the original template by multiples of the repeat unit. Here, we report on the identification of a highly polymorphic tetranucleotide repeat (named DXpS) mapping to within a CpG island on Xp. This island is 191 bp downstream from the start of the repeat element, and contains sites for the HhaI, HpaII and BstUI methyl-sensitive restriction enzymes. We developed the DXpS and the HUMARA markers into a biplex methylation-based quantitative fluorescent PCR assay. For DXpS we observed twelve alleles with negligible stuttering. DXpS exhibited a heterozygosity rate of 87% (n = 60), matching that of HUMARA. The combined informativeness of the biplex assay was 98%. Random and nonrandom X-inactivation patterns inferred with DXpS in phenotypically normal females and haemophiliac females carrying a defective F8 gene were highly concordant (r^2^ = 0.96) with HUMARA patterns. DXpS represents a notable advancement in detecting X-chromosome inactivation due to the observed high rate of heterozygosity, negligible stuttering, concordance with HUMARA, and the apparent neutrality of allelic variants. Financial support: FAPESP (09/10615-7), FAPERJ, CNPq

Cytoplasmic innate immune sensing by the caspase-4 non-canonical inflammasome promotes cellular senescence

Cytoplasmic recognition of microbial lipopolysaccharides (LPS) in human cells is elicited by the caspase-4 and caspase-5 noncanonical inflammasomes, which induce a form of inflammatory cell death termed pyroptosis. Here we show that LPS-mediated activation of caspase-4 also induces a stress response promoting cellular senescence, which is dependent on the caspase-4 substrate gasdermin-D and the tumor suppressor p53. Furthermore, we found that the caspase-4 noncanonical inflammasome is induced and assembled in response to oncogenic RAS signaling during oncogene-induced senescence (OIS). Moreover, targeting caspase-4 expression in OIS showed its critical role in the senescence-associated secretory phenotype and the cell cycle arrest induced in cellular senescence. Finally, we observed that caspase-4 induction occurs in vivo in mouse models of tumor suppression and ageing. Altogether, we are showing that cellular senescence is induced by cytoplasmic LPS recognition by the noncanonical inflammasome and that this pathway is conserved in the cellular response to oncogenic stress.This work was funded by Cancer Research UK (CRUK) (C47559/A16243 Training & Career Development Board - Career Development Fellowship), the University of Edinburgh Chancellor’s Fellowship R42576 MRC, and the Ministry of Science and Innovation of the Government of Spain (Proyecto PID2020-117860GB-I00 financiado por MCIN/ AEI /10.13039/501100011033). J.C.A. was supported by CRUK, the University of Edinburgh and is supported by the Spanish National Research Council (CSIC). P.H., I.F.D and N.T. were funded by the University of Edinburgh. A.Q. was funded by CRUK. J.F.P and A.B.L. are funded by NIH grants: 1R01AG068048-01; P01 AG062413; 1UG3 CA268103-01. J.B. was funded by BBSRC (BB/K017314/1). V.S-B is supported by funding from the University of Edinburgh and Medical Research Council (MC_UU_00009/2). F.R.M is funded by a Wellcome Trust Clinical Research Fellowship through the Edinburgh Clinical Academic Track (ECAT) (203913/Z/16/Z). M.M. was supported by CRUK Edinburgh Centre Award (C157/A25140). V.G.B. is funded by CRUK (C157/A24837) and the University of Edinburgh

Can luteal regression be reversed?

The corpus luteum is an endocrine gland whose limited lifespan is hormonally programmed. This debate article summarizes findings of our research group that challenge the principle that the end of function of the corpus luteum or luteal regression, once triggered, cannot be reversed. Overturning luteal regression by pharmacological manipulations may be of critical significance in designing strategies to improve fertility efficacy

Sialic Acid Glycobiology Unveils Trypanosoma cruzi Trypomastigote Membrane Physiology.

Trypanosoma cruzi, the flagellate protozoan agent of Chagas disease or American trypanosomiasis, is unable to synthesize sialic acids de novo. Mucins and trans-sialidase (TS) are substrate and enzyme, respectively, of the glycobiological system that scavenges sialic acid from the host in a crucial interplay for T. cruzi life cycle. The acquisition of the sialyl residue allows the parasite to avoid lysis by serum factors and to interact with the host cell. A major drawback to studying the sialylation kinetics and turnover of the trypomastigote glycoconjugates is the difficulty to identify and follow the recently acquired sialyl residues. To tackle this issue, we followed an unnatural sugar approach as bioorthogonal chemical reporters, where the use of azidosialyl residues allowed identifying the acquired sugar. Advanced microscopy techniques, together with biochemical methods, were used to study the trypomastigote membrane from its glycobiological perspective. Main sialyl acceptors were identified as mucins by biochemical procedures and protein markers. Together with determining their shedding and turnover rates, we also report that several membrane proteins, including TS and its substrates, both glycosylphosphatidylinositol-anchored proteins, are separately distributed on parasite surface and contained in different and highly stable membrane microdomains. Notably, labeling for α(1,3)Galactosyl residues only partially colocalize with sialylated mucins, indicating that two species of glycosylated mucins do exist, which are segregated at the parasite surface. Moreover, sialylated mucins were included in lipid-raft-domains, whereas TS molecules are not. The location of the surface-anchored TS resulted too far off as to be capable to sialylate mucins, a role played by the shed TS instead. Phosphatidylinositol-phospholipase-C activity is actually not present in trypomastigotes. Therefore, shedding of TS occurs via microvesicles instead of as a fully soluble form

Acute myelogenous leukemia switch lineage upon relapse to acute lymphoblastic leukemia: a case report

Acute leukemia, the most common form of cancer in children, accounts for approximately 30% of all childhood malignancies, with acute lymphoblastic leukemia being five times more frequent than acute myeloid leukemia. Lineage switch is the term that has been used to describe the phenomenon of acute leukemias that meet the standard French-American-British system criteria for a particular lineage (either lymphoid or myeloid) upon initial diagnosis, but meet the criteria for the opposite lineage at relapse. Many reports have documented conversions of acute lymphoblastic leukemia to acute myeloid leukemia

Depredación por Podisus maculiventris (Say) sobre larvas de Choristoneura rosaceana (Harris)

Choristoneura rosaceana (Harris) es una plaga del manzano Malus domestica Borkh. de reciente aparición en México. Su control depende básicamente del uso de insecticidas químicos; sin embargo, existen registros de enemigos naturales de esta plaga que ejercen un control considerable. El objetivo del estudio fue evaluar la capacidad de depredación de Podisus maculiventris (Say) sobre C. rosaceana. Para lo anterior, en agosto y septiembre de 2014, se recolectaron 1200 larvas de C. rosaceana en huertos de manzano. Asimismo, se recolectaron 87 especímenes del depredador P. maculiventris, de diferentes estadios ninfales, de los cuales 75 se recolectaron en huertos de manzano y 17 en parcelas de maíz, además se recolectaron 22 grupos de huevos (17 en maíz y cinco en manzano). Se realizaron ensayos de consumo de P. maculiventris sobre larvas de C. rosaceana, donde el promedio fue de 0.72 larvas consumidas por día, siendo el primer estadio ninfal el que mostró un mayor promedio de consumo (1.9 larvas/día), en las primeras 24 h y el segundo estadio mostró el mayor promedio a los 7 días (1.2 larvas consumidas/día).Choristoneura rosaceana (Harris) es una plaga del manzano Malus domestica Borkh. de reciente aparición en México. Su control depende básicamente del uso de insecticidas químicos; sin embargo, existen registros de enemigos naturales de esta plaga que ejercen un control considerable. El objetivo del estudio fue evaluar la capacidad de depredación de Podisus maculiventris (Say) sobre C. rosaceana. Para lo anterior, en agosto y septiembre de 2014, se recolectaron 1200 larvas de C. rosaceana en huertos de manzano. Asimismo, se recolectaron 87 especímenes del depredador P. maculiventris, de diferentes estadios ninfales, de los cuales 75 se recolectaron en huertos de manzano y 17 en parcelas de maíz, además se recolectaron 22 grupos de huevos (17 en maíz y cinco en manzano). Se realizaron ensayos de consumo de P. maculiventris sobre larvas de C. rosaceana, donde el promedio fue de 0.72 larvas consumidas por día, siendo el primer estadio ninfal el que mostró un mayor promedio de consumo (1.9 larvas/día), en las primeras 24 h y el segundo estadio mostró el mayor promedio a los 7 días (1.2 larvas consumidas/día)

Depredación por Podisus maculiventris (Say) sobre larvas de Choristoneura rosaceana (Harris)

Choristoneura rosaceana (Harris) es una plaga del manzano Malus domestica Borkh. de reciente aparición en México. Su control depende básicamente del uso de insecticidas químicos; sin embargo, existen registros de enemigos naturales de esta plaga que ejercen un control considerable. El objetivo del estudio fue evaluar la capacidad de depredación de Podisus maculiventris (Say) sobre C. rosaceana. Para lo anterior, en agosto y septiembre de 2014, se recolectaron 1200 larvas de C. rosaceana en huertos de manzano. Asimismo, se recolectaron 87 especímenes del depredador P. maculiventris, de diferentes estadios ninfales, de los cuales 75 se recolectaron en huertos de manzano y 17 en parcelas de maíz, además se recolectaron 22 grupos de huevos (17 en maíz y cinco en manzano). Se realizaron ensayos de consumo de P. maculiventris sobre larvas de C. rosaceana, donde el promedio fue de 0.72 larvas consumidas por día, siendo el primer estadio ninfal el que mostró un mayor promedio de consumo (1.9 larvas/día), en las primeras 24 h y el segundo estadio mostró el mayor promedio a los 7 días (1.2 larvas consumidas/día).Choristoneura rosaceana (Harris) es una plaga del manzano Malus domestica Borkh. de reciente aparición en México. Su control depende básicamente del uso de insecticidas químicos; sin embargo, existen registros de enemigos naturales de esta plaga que ejercen un control considerable. El objetivo del estudio fue evaluar la capacidad de depredación de Podisus maculiventris (Say) sobre C. rosaceana. Para lo anterior, en agosto y septiembre de 2014, se recolectaron 1200 larvas de C. rosaceana en huertos de manzano. Asimismo, se recolectaron 87 especímenes del depredador P. maculiventris, de diferentes estadios ninfales, de los cuales 75 se recolectaron en huertos de manzano y 17 en parcelas de maíz, además se recolectaron 22 grupos de huevos (17 en maíz y cinco en manzano). Se realizaron ensayos de consumo de P. maculiventris sobre larvas de C. rosaceana, donde el promedio fue de 0.72 larvas consumidas por día, siendo el primer estadio ninfal el que mostró un mayor promedio de consumo (1.9 larvas/día), en las primeras 24 h y el segundo estadio mostró el mayor promedio a los 7 días (1.2 larvas consumidas/día)