Publications by authors named "Jan Rozman"

Tissue homeostasis, the biological process of maintaining a steady state in tissue via control of cell proliferation and death, is essential for the development, growth, maintenance, and proper function of living organisms. Disruptions to this process can lead to serious diseases and even death. In this study, we use the vertex model for the cell-level description of tissue mechanics to investigate the impact of the tissue environment and local mechanical properties of cells on homeostasis in confined epithelial tissues.

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Complex tissue flows in epithelia are driven by intra- and inter-cellular processes that generate, maintain, and coordinate mechanical forces. There has been growing evidence that cell shape anisotropy, manifested as nematic order, plays an important role in this process. Here we extend an active nematic vertex model by replacing substrate friction with internal viscous dissipation, dominant in epithelia not supported by a substrate or the extracellular matrix, which are found in many early-stage embryos.

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We study a mixture of extensile and contractile cells using a vertex model extended to include active nematic stresses. The two cell populations phase separate over time. While phase separation strengthens monotonically with an increasing magnitude of contractile activity, the dependence on extensile activity is nonmonotonic, so that sufficiently high values reduce the extent of sorting.

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The mechanics of epithelial tissues, which is governed by forces generated in various cell regions, is often investigated using two-dimensional models that account for the apically positioned actomyosin structures but neglect basolateral mechanics. We employ a more detailed three-dimensional model to study how lateral surface tensions affect the structure and rigidity of such tissues. We find that cells are apicobasally asymmetric, with one side appearing more ordered than the other depending on target cell apical perimeter.

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Thyroid hormone (TH) effects are mediated through TH receptors (TRs), TRα1, TRβ1, and TRβ2. The TRs bind to the DNA and regulate expression of TH target genes (canonical signaling). In addition, they mediate activation of signaling pathways (noncanonical signaling).

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Restless legs syndrome (RLS) is a neurological disorder characterized by uncomfortable or unpleasant sensations in the legs during rest periods. To relieve these sensations, patients move their legs, causing sleep disruption. While the pathogenesis of RLS has yet to be resolved, there is a strong genetic association with the MEIS1 gene.

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Vertebrate neural tube closure is associated with complex changes in cell shape and behavior, however, the relative contribution of these processes to tissue folding is not well understood. At the onset of Xenopus neural tube folding, we observed alternation of apically constricted and apically expanded cells. This apical domain heterogeneity was accompanied by biased cell orientation along the anteroposterior axis, especially at neural plate hinges, and required planar cell polarity signaling.

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We study the vertex model for epithelial tissue mechanics extended to include coupling between the cell shapes and tensions in cell-cell junctions. This coupling represents an active force which drives the system out of equilibrium and leads to the formation of nematic order interspersed with prominent, long-lived +1 defects. The defects in the nematic ordering are coupled to the shape of the cell tiling, affecting cell areas and coordinations.

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Article Synopsis
  • Delta-like homolog 1 (Dlk1) inhibits fat cell formation and influences the fate of adipocyte progenitors through two key regulatory mechanisms: transcriptional and translational.* -
  • Mice lacking both Dlk1 and its orthologue SKMc15 (dKO) showed drastically reduced fat tissue and resistance to obesity from a high-fat diet, with increased Wnt signaling, which suppresses fat cell differentiation.* -
  • The study highlights how Dlk1 controls Wnt signaling for transcriptional regulation, while Ifrd2 acts as a translational inhibitor affecting Dlk1 protein levels, revealing new insights into adipocyte differentiation.*
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Inherited disorders of mitochondrial metabolism, including isolated methylmalonic aciduria, present unique challenges to energetic homeostasis by disrupting energy-producing pathways. To better understand global responses to energy shortage, we investigated a hemizygous mouse model of methylmalonyl-CoA mutase (Mmut)-type methylmalonic aciduria. We found Mmut mutant mice to have reduced appetite, energy expenditure and body mass compared with littermate controls, along with a relative reduction in lean mass but increase in fat mass.

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  • Cardiovascular diseases are a major health problem that cause many deaths worldwide, and scientists use mice to study these diseases more easily.
  • The International Mouse Phenotyping Consortium (IMPC) is working to understand how different genes affect the heart by creating special mice that are missing specific genes and testing them using advanced methods.
  • This research is helping to link genes that affect metabolism with heart health, offering new chances to discover what causes heart diseases.
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  • - The study presents the first specific reference ranges for electrocardiography (ECG) in laboratory mice, derived from a large dataset of over 26,000 C57BL/6N mice grouped by age and sex.
  • - It finds that factors like sex and age have minimal impact on key ECG metrics, while anesthesia significantly reduces heart rate.
  • - The reference ranges established for C57BL/6N mice appear applicable to various other mouse strains, providing a crucial resource for research involving cardiac function in experimental settings.
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In this study we use comparative genomics to uncover a gene with uncharacterized function (1700011H14Rik/C14orf105/CCDC198), which we hereby name FAME (Factor Associated with Metabolism and Energy). We observe that FAME shows an unusually high evolutionary divergence in birds and mammals. Through the comparison of single nucleotide polymorphisms, we identify gene flow of FAME from Neandertals into modern humans.

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Stress responses are activated by the hypothalamic-pituitary-adrenal axis (HPA axis), culminating in the release of glucocorticoids. During prolonged periods of secretion of glucocorticoids or inappropriate behavioral responses to a stressor, pathologic conditions may occur. Increased glucocorticoid concentration is linked to generalized anxiety, and there are knowledge gaps regarding its regulation.

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Vertebrate neural tube closure is associated with complex changes in cell shape and behavior, however, the relative contribution of these processes to tissue folding is not well understood. In this study, we evaluated morphology of the superficial cell layer in the neural plate. At the stages corresponding to the onset of tissue folding, we observed the alternation of cells with apically constricting and apically expanding apical domains.

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Background: Dietary carbohydrates and fats are intrinsically correlated within the habitual diet. We aimed to disentangle the associations of starch and sucrose from those of fat, in relation to allergic sensitization, asthma and rhinoconjuctivitis prevalence in humans, and to investigate underlying mechanisms using murine models.

Methods: Epidemiological data from participants of two German birth cohorts (age 15) were used in logistic regression analyses testing cross-sectional associations of starch and sucrose (and their main dietary sources) with aeroallergen sensitization, asthma and rhinoconjunctivitis, adjusting for correlated fats (saturated, monounsaturated, omega-6 and omega-3 polyunsaturated) and other covariates.

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Current concepts regarding the biology of aging are primarily based on studies aimed at identifying factors regulating lifespan. However, lifespan as a sole proxy measure for aging can be of limited value because it may be restricted by specific pathologies. Here, we employ large-scale phenotyping to analyze hundreds of markers in aging male C57BL/6J mice.

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Article Synopsis
  • Cardiometabolic diseases like type 2 diabetes and cardiovascular disease significantly impact public health, and understanding the genetic control of proteins linked to these diseases may reveal their underlying biology.
  • Researchers conducted a protein quantitative trait locus (pQTL) analysis on 248 serum proteins in nearly 3,000 individuals from two Greek cohorts, identifying 301 pQTL variants associated with 170 proteins, including 12 rare variants.
  • They found specific proteins tied to cardiometabolic traits, such as Mep1b linked to HDL levels, and created a Mep1b knockout mouse model, highlighting the value of studying isolated populations for genetic research.
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The forced oscillation technique (FOT) is a powerful and accurate method to quantify the mechanical properties of the airways and tissues of the respiratory system. Here we provide a detailed protocol for the measurement of mouse respiratory mechanical parameters. We present a procedure for mouse endotracheal intubation using a handcrafted intubation platform and confirmation module.

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Cold and nutrient-activated brown adipose tissue (BAT) is capable of increasing systemic energy expenditure via the uncoupled respiration and secretion of endocrine factors, thereby protecting mice against diet-induced obesity and improving insulin response and glucose tolerance in men. Long non-coding RNAs (lncRNAs) have recently been identified as fine-tuning regulators of cellular function. While certain lncRNAs have been functionally characterised in adipose tissue, their overall contribution in the activation of BAT remains elusive.

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Article Synopsis
  • Daily torpor is a way for animals like common swifts to save energy by resting and lowering their body temperature.
  • Scientists studied these birds in their nests over several years and found that their body temperature often dropped significantly when they were in torpor.
  • They used special equipment to measure how much energy the swifts used during torpor and discovered that their energy use could be reduced by over half, helping them conserve energy during colder nights.
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Clonal dominance arises when the descendants (clones) of one or a few founder cells contribute disproportionally to the final structure during collective growth [1-8]. In contexts such as bacterial growth, tumorigenesis, and stem cell reprogramming [2-4], this phenomenon is often attributed to pre-existing propensities for dominance, while in stem cell homeostasis, neutral drift dynamics are invoked [5,6]. The mechanistic origin of clonal dominance during development, where it is increasingly documented [1,6-8], is less understood.

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Article Synopsis
  • - The study investigates the genetic factors underlying congenital heart disease by screening nearly 3,900 mouse gene mutations for cardiac issues, finding 705 lines with conditions like arrhythmia and myocardial hypertrophy.
  • - Out of these, 486 genes are newly linked to heart dysfunction, including variants of unknown relevance (VUR), with specific mutations in five genes (Casz1, Dnajc18, Pde4dip, Rnf38, Tmem161b) leading to notable structural heart defects.
  • - Using data from the UK Biobank, the research further confirms the role of the DNAJC18 gene in heart function, highlighting its loss as linked to changes in cardiac performance, thus identifying new potential targets for understanding
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