Intracellular action of the cytokine MIF to modulate AP-1 activity and the cell cycle through Jab1
By R. Kleemann, A. Hausser, Georg Geiger, R. Mischke, A. Burger-Kentischer, O. Flieger, F. Johannes, T. Roger, Thierry Calandra, A. Kapurniotu and 4 more. Nature, 2000
595 citations recorded by the source corpus.
Subfields: Cellular and Molecular Neuroscience, Immunology
View Paper: https://www.semanticscholar.org/paper/d359db8f27e964c372208efc0b83a79478f87e34
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In Cellular and Molecular Neuroscience
In Immunology
Citations in the corpus
- Macrophage migration inhibitory factor: a regulator of innate immunity (2003, unknown): “Second, the article by Kleemann et al.53 assigns growth-inhibitory and anti-inflammatory functions to MIF that go against what were thought to be two well-established properties of MIF — that is, its capacity to sustain cell growth and to induce proinflammatory responses.”
- The ubiquitin-proteasome proteolytic pathway: destruction for the sake of construction. (2002, background): “causes a reversal in CSN5/JAB1 activity, leading to CSN5/ JAB1-dependent increase in p27 (235).”
- MIF is a noncognate ligand of CXC chemokine receptors in inflammatory and atherogenic cell recruitment (2007, background): “and intracellularly interacts with c-Jun activation domain binding protein-1 (JAB1) (ref”
- MIF regulates innate immune responses through modulation of Toll-like receptor 4 (2001, background): “Given that MIF has been shown to exert intracellular activit”
- MIF Signal Transduction Initiated by Binding to CD74 (2003, methodology): “Whether the binding of MIF to CD74 accounts for all of MIF’s cellular actions is unknown, and perhaps unlikely in light of experiments suggesting a pathway for MIF internalization and binding to Jab1 (30), and continued interest in the biological function of MIF’s NH2-terminal, catalytic domain (28)”
- Investigations on DNA intercalation and surface binding by SYBR Green I, its structure determination and methodological implications. (2004, methodology): “Human embryonal kidney 293 T cells (25) were grown overnight in serum-derived medium RPMI-1640 from Invitrogen Life Technologies (Karlsruhe, Germany) and used as a source for total RNA.”
- CD44 is the signaling component of the macrophage migration inhibitory factor-CD74 receptor complex. (2006, background): “, 2001), controls Jab1 transcriptional effects (Kleemann et al., 2000), and suppresses activation-induced, p53-dependent apoptosis (Hudson et al.”