Publications by authors named "T Goncharov"

Receptor-interacting protein 1 (RIP1, RIPK1) is a critical mediator of multiple signaling pathways that promote inflammatory responses and cell death. The kinase activity of RIP1 contributes to the pathogenesis of a number of inflammatory and neurodegenerative diseases. However, the role of RIP1 in retinopathies remains unclear.

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Ubiquitination is a posttranslational modification that is crucial for the dynamic regulation of diverse signaling pathways. To enhance our understanding of ubiquitination-mediated signaling, we generated a new class of bispecific antibodies that combine recognition of ubiquitination substrates and specific polyubiquitin linkages. RIP1-K63 and RIP1-linear (Lin) linkage polyubiquitin bispecific antibodies detected linkage-specific ubiquitination of the proinflammatory kinase RIP1 in cells and in tissues and revealed RIP1 ubiquitination by immunofluorescence.

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Article Synopsis
  • Graft-versus-host disease (GVHD) is a major complication after hematopoietic cell transplantation, causing significant morbidity and mortality, often mediated by inflammatory cytokines affecting crucial cells like intestinal stem cells.
  • The study explored the role of receptor interacting protein kinase 1 (RIP1) in acute GVHD, finding that high levels of phospho-RIP1 in patient biopsies indicated tissue damage and increased nonrelapse mortality, while blocking RIP1 helped protect stem cells and reduced inflammation in GVHD target organs.
  • Inhibiting RIP1, either genetically or with the compound GNE684, improved long-term survival in mouse models without compromising the beneficial graft-versus-leukemia effect, suggesting that RIP1
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XIAP is a caspase-inhibitory protein that blocks several cell death pathways, and mediates proper activation of inflammatory NOD2-RIP2 signaling. XIAP deficiency in patients with inflammatory diseases such as Crohn's disease, or those needing allogeneic hematopoietic cell transplantation, is associated with a worse prognosis. In this study, we show that XIAP absence sensitizes cells and mice to LPS- and TNF-mediated cell death without affecting LPS- or TNF-induced NF-κB and MAPK signaling.

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This paper presents a comparative analysis of HS sensor properties of nanocrystalline SnO modified with Ag nanoparticles (AgNPs) as reference sample or Ag organic complexes (AgL1 and AgL2). New hybrid materials based on SnO and Ag(I) organometallic complexes were obtained. The microstructure, compositional characteristics and thermal stability of the composites were thoroughly studied by X-ray diffraction (XRD), X-ray fluorescent spectroscopy (XRF), Raman spectroscopy, Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS) and Thermogravimetric analysis (TGA).

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