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Biology subjects

Kummer, S.

Publications and source records attributed to Kummer, S..

10 recordsLinked to original sources

Domain-adversarial learning predicts clinically actionable drug combination synergy in leukemia patients using bulk transcriptomics data

Deep learning has gained popularity in drug combination synergy prediction; however, DL models require large training datasets from cell line pharmacogenomic screens that poorly capture the heterogeneity in transcriptomic features and phenotypic responses seen in patients. To that end, we developed a domain-adversarial neural network (DANN) for personalized drug synergy prediction that accounts for systematic differences between cell line and patient domains. In applications to AML and CLL patient samples, we demonstrate how DANN boosts prediction accuracy under realistic data constraints. The model predictions demonstrated elevated synergy among clinically used combinations, such as venetoclax-based regimens, supporting its ability to identify both pharmaceutically and clinically meaningful combinations. DANN estimates prediction uncertainty and prioritizes high-confidence combination predictions to aid clinical translation. Together, DANN provides a systematic approach to improving accuracy and reliability in cross-domain drug synergy prediction, advancing the development of methods that are aligned with the translational requirements of precision hematology.

cancer biology↗

Cancer pathway connectivity resolved by drug perturbation and RNA sequencing

Pathway inhibitors are a backbone of cancer treatment. The configuration of pathway dependencies varies from tumour to tumour. Better treatment for individual patients could be designed if the pathway wiring were readily measurable. Here, we characterise the transcriptional responses of 116 lymphoma patient samples exposed to ten drug perturbations. We used factor analysis to decompose individual and shared drug effects, thereby generating a pathway connectivity map of chronic lymphocytic leukemia (CLL). The expression profiles of the major disease subgroups, defined by IGHV mutation status, became more similar to each other after BTK inhibition, consistent with B-cell receptor (BCR) signalling as a driver of their phenotypic difference. An even stronger convergence was observed with combined IRAK4 and BTK inhibition, indicating cooperation of BCR and toll-like receptor (TLR) signalling in CLL. We identified genetic aberrations (BRAF, TP53, deletion 17p, deletion 15q, trisomy 12) that modulated drug effects in CLL and constituted specific interaction patterns. IRAK4 inhibition effects depended on the presence of trisomy 12, a finding that suggests that the trisomy 12 driver event in CLL acts by gene dosage-dependent IRAK4 upregulation and amplification of the BCR/TLR cooperation. Our results highlight the potential of systematic drug perturbation assays with transcriptome readout to map pathway interconnectivity and functionally annotate tumour drivers.

systems biology↗

Detection of vasculogenic mimicry in equine ocular, oronasal, and genital squamous cell carcinoma

Squamous cell carcinoma (SCC) is the most common malignant tumor disease in horses. It predominantly affects the ocular, oronasal, and anogenital region. Equine SCC is difficult to treat, also because important aspects of SCC development and metastasis are still unclear. We previously provided evidence that equine SCC cells can adopt a stem cell-like phenotype as a hallmark of malignant progression. Here, we investigated whether equine SCCs harbor endothelial-like tumor cells that form an alternative network of pseudo-vessels better known as vasculogenic mimicry (VM). Following histopathological diagnosis, 43 equine SCCs or precursor lesions (15 ocular, 14 genital, 14 oronasal tumors) were PCR-screened for equine papillomavirus (EcPV) infection. Subsequently, formalin-fixed paraffin-embedded-sections of all tumors were analyzed by Periodic Acid-Schiff (PAS) reaction and immunohistochemical (IHC) staining for endothelial cell marker CD31. Obtained micrographs were evaluated by a scientific board to unanimously identify sections of intact tumor tissue displaying PAS-positive, CD31-negative lumens harboring erythrocytes. Thirteen lesions exhibiting these features were subjected to triple immunofluorescence (IF) staining for CD31, pan-cytokeratin (KRT) and type 4 collagen (Col4) or alpha smooth muscle actin (SMA) to confirm the presence of VM, and to determine whether pericytes have a role in this phenomenon. All genital and 50% of oronasal lesions scored positive for EcPV type 2, whilst ocular lesions tested negative. One mandibular SCC harbored EcPV type 5. Six genital, three oronasal, and four ocular tumors unambiguously exhibited VM as revealed by CD31-/PAS+ vessel-like structures containing erythrocytes, the detection of CD31-negative cells lining their lumens, and the presence of Col4 and SMA in this lining. Detection of these two proteins in the context of VM suggests that VM-forming cancer cells recruit pericytes to enhance channel formation and stability. To our knowledge, this is the first report providing evidence of VM in equine cancer, and more generally, SCC in animals.

cancer biology↗

Human airway organoids as a versatile model to study BSL-4 virus replication and pathogenesis

Research with BSL-4 viruses such as Ebola, Marburg, and Nipah presents significant challenges due to their high virulence and the stringent containment measures required. A major limitation in studying viral pathogenesis and developing therapeutic strategies is the absence of suitable animal models that accurately replicate human disease. In this context, 3D cell culture systems offer significant advantages over traditional 2D monolayer cultures, mimicking native physiological conditions including cell polarization and composition. Human airway organoids, derived from pluripotent or adult stem cells, closely replicate the structure and function of the human respiratory system, providing a relevant and accessible environment for studying viral replication and pathogenesis. In contrast to conventional cell lines, airway organoids enable investigation of virus-host interactions within a human tissue context, providing insights that are more directly translatable to human disease. In our study, we generated airway organoids from both clinical donor tissues and commercially available nasal epithelial cells and showed in comparative analyses with whole lung tissue that these organoids are comparable in terms of cell composition. Despite donor-specific variations due to genetic factors, airway organoids derived from different sources and donors exhibit a remarkably similar cellular make-up. We further demonstrated that organoids derived from nasal swabs can effectively replicate BSL-4 viruses, establishing them as a standardized 3D model for broader research applications and advancing our understanding of these pathogens, especially in the absence of reliable animal models. Author SummaryThis study establishes human airway organoids as a robust model for investigating BSL-4 pathogens, such as Ebola, Marburg, and Nipah virus. Airway organoids represent reliable systems due to their ability to replicate the complexity of human respiratory epithelia and support viral infection. These organoids exhibit high susceptibility to these viruses, allowing for subsequent analysis of infection kinetics, immune evasion, and tissue-specific tropism within a controlled environment. This platform provides a powerful tool for antiviral testing and studying virus-host interactions, thus helping bridge critical gaps in high-containment virus research.

cell biology↗

The phenuivirus Toscana virus makes an atypical use of vacuolar acidity to enter host cells

Toscana virus is a major cause of arboviral disease in humans in the Mediterranean basin during summer. However, early virus-host cell interactions and entry mechanisms remain poorly characterized. Investigating iPSC-derived human neurons and cell lines, we found that virus binding to the cell surface was specific but inefficient, and 50% of bound virions were endocytosed within 10 min. Virions entered Rab5a+ early endosomes and, subsequently, Rab7a+ and LAMP-1+ late endosomal compartments. Penetration required intact late endosomes and occurred within 30 min following internalization. Virus entry relied on vacuolar acidification, with an optimal pH for viral membrane fusion at pH 5.5. The pH threshold increased to 5.8 with longer pre-exposure of virions to the slightly acidic pH in early endosomes. Strikingly, the particles remained infectious after entering late endosomes with a pH below the fusion threshold. Overall, our study establishes Toscana virus as a late-penetrating virus and reveals an atypical use of vacuolar acidity by this virus to enter host cells.

microbiology↗

Prefrontal accumbens neural dynamics abnormalities in mice vulnerable to develop food addiction

Food addiction is characterized by a loss of behavioral control over food intake and is closely associated with several eating disorders, including obesity and binge eating. Despite its high prevalence, the underlying neural mechanisms of food addiction are still unresolved. We trained mice in an operant paradigm for 110 days to promote the development of food addiction. Then, we classified mice as addicted and extreme non-addicted based on three addiction criteria and recorded neural activities in the prelimbic medial prefrontal cortex (mPFC) and nucleus accumbens (NAc) core through electrophysiology in vivo. Addicted mice presented disrupted mPFC-to-NAc signaling at high frequencies (hfo 150-200 Hz) during decision-making to obtain food. Moreover, addicted mice exhibited reduced low gamma oscillations and theta-gamma coupling in the NAc during reward expectancy. Disrupted mPFC-to-NAc connectivity and gamma synchrony in the NAc correlated with increased reinforcement levels, unraveling the functional relevance of these alterations. The cannabinoid type-1 (CB1) receptor antagonist rimonabant rescued neural alterations observed in the addicted mice.Reinforcement levels were reduced after rimonabant administration and the directionality of signals and oscillatory activity in the NAc were reversed in addicted mice during decision-making and reward expectation, respectively. These findings suggest that disrupted mPFC-NAc neural dynamics are candidate mechanisms underlying specific behavioral alterations associated with food addiction. The elucidation of these novel communication mechanisms between the mPFC and the NAc will provide advances towards future development of new therapeutic interventions for food addiction and related disorders.

animal behavior and cognition↗

TRIM 25 nuclear translocation is hampered by localization to influenza A virus non-structural protein 1 cytosolic aggregates

Non-structural protein 1 (NS1) of influenza A virus (IAV) is involved in multiple blocking processes of cellular antiviral action. One of these includes the binding of cytosolic tripartite motif-containing protein 25 (TRIM25) to impede nuclear translocation and, thus, counteracting the block of viral RNA elongation taking place inside the nucleus. In addition, TRIM25 is part of the RIG-I signaling pathway and is an important component regarding the activation of interferon-induced genes and triggering cellular antiviral responses. In this study, we focus on the spatial localization of TRIM25 with respect to cytosolic NS1 aggregates found in IAV infected cells. Besides strain specific characteristics, we confirmed co-localization of TRIM25 to NS1 cytosolic aggregates at 16 hours post infection for all investigated IAV strains based on image analysis on single cell level. Immunoprecipitation further confirmed the interaction between NS1 and TRIM25 when comparing wt IAV and recombinant IAV devoid of NS1 expression. Of note, we combined fluorescence in situ hybridization targeting viral RNA with immunolabeling of TRIM25 suitable for nanoscopy and the diffraction limited detection of NS1 in one imaging approach. Our study reveals strain dependent differences in the block of IRF3 activation in respect to the accumulation of TRIM25 in cytosolic NS1 aggregates.

microbiology↗

The native structure of the full-length, assembled influenza A virus matrix protein, M1.

Influenza A virus causes millions of severe illnesses during annual epidemics. The most abundant protein in influenza virions is the matrix protein M1 that mediates virus assembly by forming an endoskeleton beneath the virus membrane. The structure of full-length M1, and how it oligomerizes to mediate assembly of virions, is unknown. Here we have determined the complete structure of assembled M1 within intact virus particles, as well as the structure of M1 oligomers reconstituted in vitro. We found that the C-terminal domain of M1 is disordered in solution, but can fold and bind in trans to the N-terminal domain of another M1 monomer, thus polymerising M1 into linear strands which coat the interior surface of the assembling virion membrane. In the M1 polymer, five histidine residues, contributed by three different M1 monomers, form a cluster that can serve as the pH-sensitive disassembly switch after entry into a target cell. These structures therefore provide mechanisms for influenza virus assembly and disassembly.

biochemistry↗

Protective role of neuronal and lymphoid cannabinoid CB2 receptors in neuropathic pain

Cannabinoid CB2 receptor (CB2r) agonists are potential painkillers void of psychotropic effects. Peripheral immune cells, neurons and glia express CB2r, however the involvement of CB2r from these cells in neuropathic pain remains unresolved. We explored spontaneous neuropathic pain through on-demand self-administration of the selective CB2r agonist JWH133 in wild-type and knockout mice lacking CB2r in neurons, monocytes or constitutively. Operant self-administration reflected drug-taking to alleviate spontaneous pain, nociceptive and affective manifestations. While constitutive deletion of CB2r disrupted JWH133-taking behavior, this behavior was not modified in monocyte-specific CB2r knockouts and was increased in mice defective in neuronal CB2r knockouts suggestive of increased spontaneous pain. Interestingly, CB2r-positive lymphocytes infiltrated the injured nerve and possible CB2r transfer from immune cells to neurons was found. Lymphocyte CB2r depletion also exacerbated JWH133 self-administration and inhibited antinociception. This work identifies a simultaneous activity of neuronal and lymphoid CB2r that protects against spontaneous and evoked neuropathic pain.

physiology↗

Flat-to-curved transition during clathrin-mediated endocytosis correlates with a change in clathrin-adaptor ratio and is regulated by membrane tension

Although essential for many cellular processes, the sequence of structural and molecular events during clathrin-mediated endocytosis remains elusive. While it was believed that clathrin-coated pits grow with a constant curvature, it was recently suggested that clathrin first assembles to form a flat structure and then bends while maintaining a constant surface area. Here, we combine correlative electron and light microscopy and mathematical modelling to quantify the sequence of ultrastructural rearrangements of the clathrin coat during endocytosis in mammalian cells. We confirm that clathrin-coated structures can initially grow flat and that lattice curvature does not show a direct correlation with clathrin coat assembly. We demonstrate that curvature begins when 70% of the final clathrin content is acquired. We find that this transition is marked by a change in the clathrin to clathrin-adaptor protein AP2 ratio and that membrane tension suppresses this transition. Our results support the model that mammalian cells dynamically regulate the flat-to-curved transition in clathrin-mediated endocytosis by both biochemical and mechanical factors.

cell biology↗