Publications by authors named "J N Eble"

Rapid progress has been made in the exciting field of secretome research in health and disease. The tumor secretome, which is a significant proportion of the tumor proteome, is secreted into the extracellular space to promote intercellular communication and thus tumor progression. Among the many molecules of the secretome, integrins and matrix metalloproteinase 14 (MMP14) stand out as the interplay of adhesion and proteolysis drives invasion.

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Renowned for their role in haemostasis and thrombosis, platelets are also increasingly recognized for their contribution in innate immunity, immunothrombosis and inflammatory diseases. Platelets express a wide range of receptors, which allows them to reach a variety of activation endpoints and grants them immunomodulatory functions. Activated platelets release extracellular vesicles (PEVs), whose formation and molecular cargo has been shown to depend on receptor-mediated activation and environmental cues.

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Introduction: Osteoclasts determine bone tissue turnover. Their increased activity causes osteoporosis, their dysfunction osteopetrosis.

Methods And Results: Murine monocytic ER-Hoxb8 cells differentiate into OCs upon treatment with M-CSF and RANKL and upregulate the collagen-binding integrin α2β1 distinctly earlier than other OC markers, such as the OC-associated receptor, OSCAR.

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Article Synopsis
  • Aberrant gene expression in acute myeloid leukemia (AML) with translocations is linked to the dysregulation of epigenetic modifiers, specifically involving the AML1/ETO fusion protein.
  • The study aimed to pinpoint critical epigenetic modifiers essential for the survival and growth of AML1/ETO-positive AML cells through shRNA library screens and transcriptomics.
  • Researchers identified and validated 41 essential genes, including DNMT1 and ATR, which can be inhibited by specific drugs, showing potential for effective treatment strategies in AML1/ETO-positive patients.
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