2004
DOI: 10.1074/jbc.m312757200
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Functional Expression of the Interleukin-11 Receptor α-Chain and Evidence of Antiapoptotic Effects in Human Colonic Epithelial Cells

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Cited by 62 publications
(34 citation statements)
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“…However, as the receptors of these cytokines and growth factors are present on both innate and acquired cells, activation of STAT3 is likely to occur in both cell types [5,14,[34][35][36]57,58] . Therefore, as the function of STAT3 is a double-edged sword, careful attention should be directed toward the cell population that is being targeted when one contemplates STAT3 inhibition or activation in human IBD [59] .…”
Section: Resultsmentioning
confidence: 99%
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“…However, as the receptors of these cytokines and growth factors are present on both innate and acquired cells, activation of STAT3 is likely to occur in both cell types [5,14,[34][35][36]57,58] . Therefore, as the function of STAT3 is a double-edged sword, careful attention should be directed toward the cell population that is being targeted when one contemplates STAT3 inhibition or activation in human IBD [59] .…”
Section: Resultsmentioning
confidence: 99%
“…In contrast, GH and IL-11, both of which activate STAT3 predominantly in CECs, contribute to the suppression of experimental colitis [33][34][35] . Of note, human trials utilizing GH, IL-11 and anti-IL-6R mAb have been conducted and have shown that the strategies using these products are beneficial to IBD patients [38][39][40] (Figure 1).…”
Section: The Role Of Stat3-activators On Ibdmentioning
confidence: 99%
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“…The underlying mechanism is considered to relate to the dampening effects of IL-11 on the inflammatory response by reducing macrophage cytokine and reactive oxygen species production (Redlich et al 1996;Trepicchio et al 1996;Waxman et al 1998Waxman et al , 2003Zheng et al 2001). Moreover, IL-11 was recently shown to mediate direct antiapoptotic effects on human colonic epithelial cells (Kiessling et al 2004). IL-11 also prevents cartilage matrix degradation in chronically inflamed joints by inducing the expression of tissue inhibitor of metalloproteinases (TIMP) (Maier et al 1993) and is an important regulator of bone remodeling (Elias et al 1995;Takeuchi et al 2002).…”
Section: Introductionmentioning
confidence: 99%
“…Binding of IL-11 to IL11RA triggers heterodimerization, tyrosine phosphorylation, and activation of gp130 (Fourcin et al, 1994). The activated IL11RA -gp130 receptor complex further activates Jak family of tyrosine kinases, JAK1, JAK2, and TYK2 (Bao et al, 2006;Kiessling et al, 2004;Berger et al, 1994). JAK2 catalyzes the phosphorylation and nuclear translocation of STAT3 and STAT1 (Idris et al, 2012;Tenney et al, 2005).…”
Section: Discussionmentioning
confidence: 99%