Neurorosettes: a novel computational modelling framework to investigate the Homer-Wright rosette formation in neuroblastoma

Cancer deregulates the interactions between cells and their microenvironment, leading to disrupted architectures. Homer-Wright rosettes, observed in neuroblastoma, comprise radial arrangements of neurons surrounding a meshwork of fibres. Currently, scientists believe that the presence of Homer-Wright rosettes reflects aberrant neuronal differentiation. Nonetheless, additional understanding of how these structures develop is required since neither experimental nor computational research has characterised this mechanism properly. In this work, we propose a mechanics-based computational framework to investigate Homer-Wright rosette formation. Our model depicts neurons as a combination of spherical (cell bodies) and cylindrical (neurites) agents, and it includes proliferation, neuronal differentiation, and adhesion/repulsion dynamics between neurons. We implemented our framework as an open-source user-friendly Python package called neurorosettes that provides real-time rendering of simulation results, making it adequate for general researchers to test and visualize hypotheses of Homer-Wright rosette formation. Furthermore, we present three example use-cases to replicate the emergence of this rosette subtype and investigate how mechanical interactions between neurons and neuronal differentiation may regulate its architecture. Due to the spare amount of experimental data on the formation of these histological patterns, our applications serve primarily as preliminary examples of how our tool can be used and extended. Although our preliminary results show the relevance of mechanical interactions and poor neuronal differentiation to Homer-Wright rosette formation, these factors appear to only predict the initial stages of rosette formation. Overall, our tool can improve the theoretical knowledge on this process and drive the design of new experimental studies to validate model results

Collagen Density Regulates Tumour Spheroid Growth Through Cell Motility: A Computational Study

We aim to define the role of matrix density on tumour growth through a discrete computational framework. We integrate experimental data to characterize the dynamics of individual cellular movement, accounting for the mechanical properties of the ECM, and we evaluate how the emerging trends modulate the growth of multicellular structures

Collagen Density Regulates Tumour Spheroid Growth Through Cell Motility: A Computational Study

We aim to define the role of matrix density on tumour growth through a discrete computational framework. We integrate experimental data to characterize the dynamics of individual cellular movement, accounting for the mechanical properties of the ECM, and we evaluate how the emerging trends modulate the growth of multicellular structures

Impact of interstitial lung disease on the survival of systemic sclerosis with pulmonary arterial hypertension

To assess severity markers and outcomes of patients with systemic sclerosis (SSc) with or without pulmonary arterial hypertension (PAH-SSc/non-PAH-SSc), and the impact of interstitial lung disease (ILD) on PAH-SSc. Non-PAH-SSc patients from the Spanish SSc registry and PAH-SSc patients from the Spanish PAH registry were included. A total of 364 PAH-SSc and 1589 non-PAH-SSc patients were included. PAH-SSc patients had worse NYHA-functional class (NYHA-FC), worse forced vital capacity (FVC) (81.2 ± 20.6% vs 93.6 ± 20.6%, P < 0.001), worse tricuspid annular plane systolic excursion (TAPSE) (17.4 ± 5.2 mm vs 19.9 ± 6.7 mm, P < 0.001), higher incidence of pericardial effusion (30% vs 5.2%, P < 0.001) and similar prevalence of ILD (41.8% vs. 44.9%). In individuals with PAH-SSc, ILD was associated with worse hemodynamics and pulmonary function tests (PFT). Up-front combination therapy was used in 59.8% and 61.7% of patients with and without ILD, respectively. Five-year transplant-free survival rate was 41.1% in PAH-SSc patients and 93.9% in non-PAH-SSc patients (P < 0.001). Global survival of PAH-SSc patients was not affected by ILD regardless its severity. The multivariate survival analysis in PAH-SSc patients confirmed age at diagnosis, worse NYHA-FC, increased PVR, reduced DLCO, and lower management with up-front combination therapy as major risk factors. In conclusion, in PAH-SSc cohort risk of death was greatly increased by clinical, PFT, and hemodynamic factors, whereas it was decreased by up-front combination therapy. Concomitant ILD worsened hemodynamics and PFT in PAH-SSc but not survival regardless of FVC impairment

Impact of interstitial lung disease on the survival of systemic sclerosis with pulmonary arterial hypertension

To assess severity markers and outcomes of patients with systemic sclerosis (SSc) with or without pulmonary arterial hypertension (PAH-SSc/non-PAH-SSc), and the impact of interstitial lung disease (ILD) on PAH-SSc. Non-PAH-SSc patients from the Spanish SSc registry and PAH-SSc patients from the Spanish PAH registry were included. A total of 364 PAH-SSc and 1589 non-PAH-SSc patients were included. PAH-SSc patients had worse NYHA-functional class (NYHA-FC), worse forced vital capacity (FVC) (81.2 +/- 20.6% vs 93.6 +/- 20.6%, P < 0.001), worse tricuspid annular plane systolic excursion (TAPSE) (17.4 +/- 5.2 mm vs 19.9 +/- 6.7 mm, P < 0.001), higher incidence of pericardial effusion (30% vs 5.2%, P < 0.001) and similar prevalence of ILD (41.8% vs. 44.9%). In individuals with PAH-SSc, ILD was associated with worse hemodynamics and pulmonary function tests (PFT). Up-front combination therapy was used in 59.8% and 61.7% of patients with and without ILD, respectively. Five-year transplant-free survival rate was 41.1% in PAH-SSc patients and 93.9% in non-PAH-SSc patients (P < 0.001). Global survival of PAH-SSc patients was not affected by ILD regardless its severity. The multivariate survival analysis in PAH-SSc patients confirmed age at diagnosis, worse NYHA-FC, increased PVR, reduced DLCO, and lower management with up-front combination therapy as major risk factors. In conclusion, in PAH-SSc cohort risk of death was greatly increased by clinical, PFT, and hemodynamic factors, whereas it was decreased by up-front combination therapy. Concomitant ILD worsened hemodynamics and PFT in PAH-SSc but not survival regardless of FVC impairment

Clustering COVID-19 ARDS patients through the first days of ICU admission. An analysis of the CIBERESUCICOVID Cohort

Background Acute respiratory distress syndrome (ARDS) can be classified into sub-phenotypes according to different inflammatory/clinical status. Prognostic enrichment was achieved by grouping patients into hypoinflammatory or hyperinflammatory sub-phenotypes, even though the time of analysis may change the classification according to treatment response or disease evolution. We aimed to evaluate when patients can be clustered in more than 1 group, and how they may change the clustering of patients using data of baseline or day 3, and the prognosis of patients according to their evolution by changing or not the cluster.Methods Multicenter, observational prospective, and retrospective study of patients admitted due to ARDS related to COVID-19 infection in Spain. Patients were grouped according to a clustering mixed-type data algorithm (k-prototypes) using continuous and categorical readily available variables at baseline and day 3.Results Of 6205 patients, 3743 (60%) were included in the study. According to silhouette analysis, patients were grouped in two clusters. At baseline, 1402 (37%) patients were included in cluster 1 and 2341(63%) in cluster 2. On day 3, 1557(42%) patients were included in cluster 1 and 2086 (57%) in cluster 2. The patients included in cluster 2 were older and more frequently hypertensive and had a higher prevalence of shock, organ dysfunction, inflammatory biomarkers, and worst respiratory indexes at both time points. The 90-day mortality was higher in cluster 2 at both clustering processes (43.8% [n = 1025] versus 27.3% [n = 383] at baseline, and 49% [n = 1023] versus 20.6% [n = 321] on day 3). Four hundred and fifty-eight (33%) patients clustered in the first group were clustered in the second group on day 3. In contrast, 638 (27%) patients clustered in the second group were clustered in the first group on day 3.Conclusions During the first days, patients can be clustered into two groups and the process of clustering patients may change as they continue to evolve. This means that despite a vast majority of patients remaining in the same cluster, a minority reaching 33% of patients analyzed may be re-categorized into different clusters based on their progress. Such changes can significantly impact their prognosis

Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis

Altres ajuts: Fondo Europeo de Desarrollo Regional (FEDER), "A way of making Europe".Copy number (CN) polymorphisms of complement C4 play distinct roles in many conditions, including immune-mediated diseases. We investigated the association of C4 CN with systemic sclerosis (SSc) risk. Imputed total C4, C4A, C4B, and HERV-K CN were analyzed in 26,633 individuals and validated in an independent cohort. Our results showed that higher C4 CN confers protection to SSc, and deviations from CN parity of C4A and C4B augmented risk. The protection contributed per copy of C4A and C4B differed by sex. Stronger protection was afforded by C4A in men and by C4B in women. C4 CN correlated well with its gene expression and serum protein levels, and less C4 was detected for both in SSc patients. Conditioned analysis suggests that C4 genetics strongly contributes to the SSc association within the major histocompatibility complex locus and highlights classical alleles and amino acid variants of HLA-DRB1 and HLA-DPB1 as C4-independent signals

Encuentro Invesderm. Estableciendo Redes de Investigación en Deontología

Datos técnicos: 388 minutos, color, español. Ficha técnica: Gabinete de Presidencia CSIC y Departamento de Comunicación. Emitido en directo el 5 junio 2024INVESDERM es la primera acción conjunta entre la Academia Española de Dermatología y Venereología (AEDV) y el Consejo Superior de Investigaciones Científicas (CSIC) para establecer puentes entre investigadores básicos y clínicos en el área de la Dermatología y la Venereología. Esta reunión pretende ser una puesta en común de algunos investigadores del CSIC y de la AEDV, contando lo que hacen, lo que cada uno puede ofrecer, las carencias detectadas y las posibilidades de interacción en un contexto de investigación traslacional. El programa de INVESDERM2024 se estructura en 4 mesas redondas dinámicas, en las que los moderadores y ponentes intentarán conectar con los asistentes y motivar la interacción entre todos en los espacios. El objetivo es establecer lazos y gérmenes de colaboración entre investigadores básicos y clínicos.N

Binary systems and their nuclear explosions

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