Publications by authors named "C Sprissler"

Metacaspases (MCAs) are cysteine peptidases expressed in plants, fungi and protozoa, with a caspase-like histidine-cysteine catalytic dyad, but differing from caspases, for example, in their substrate specificity. The role of MCAs is subject to debate: roles in cell cycle control, in cell death or even in cell survival have been suggested. In this study, using a Leishmania major MCA-deficient strain, we showed that L.

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The spleen tyrosine kinase (SYK) was identified as an oncogenic driver in a broad spectrum of hematologic malignancies. The in vivo comparison of three SYK containing oncogenes, SYK(wt), TEL-SYK and IL-2-inducible T-cell kinase (ITK)-SYK revealed a general myeloexpansion and the establishment of three different hematologic (pre)diseases. SYK(wt) enhanced the myeloid and T-cell compartment, without leukemia/lymphoma development.

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Article Synopsis
  • * Mice with T cell-specific ITK-Syk expression develop aggressive T cell lymphoproliferation and B cell expansion much earlier than previously observed in other models.
  • * The early aggressive phenotype is linked to low levels of Blimp-1 induction due to ITK-Syk expression, while high levels promote T cell differentiation that prevents malignancy, suggesting a delicate balance in oncogene expression is crucial for cancer development.
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Article Synopsis
  • Peripheral T-cell lymphomas (PTCL) are hard to treat and can be deadly because regular chemotherapy doesn't work well on them.
  • Scientists found a mutation called ITK-SYK in a lot of PTCL cases and discovered it causes T-cell diseases in mice, with symptoms popping up just weeks after infection.
  • They showed that blocking the SYK protein's activity can stop the disease, suggesting that targeting this mutation could be a good treatment option for people with similar cancer types.
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In lysine biosynthesis, dihydrodipicolinate reductase (DHDPR) catalyses the formation of tetrahydrodipicolinate. Unlike DHDPR enzymes from Escherichia coli and Mycobacterium tuberculosis, which have dual specificity for both NADH and NADPH as co-factors, the enzyme from Thermotoga maritima has a significantly greater affinity for NADPH. Despite low sequence identity with the E.

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