scholarly journals Type 2 Interleukin-4 Receptor Signaling in Neutrophils Antagonizes Their Expansion and Migration during Infection and Inflammation

Immunity ◽  
2016 ◽  
Vol 45 (1) ◽  
pp. 172-184 ◽  
Author(s):  
Janine Woytschak ◽  
Nadia Keller ◽  
Carsten Krieg ◽  
Daniela Impellizzieri ◽  
Robert W. Thompson ◽  
...  
2008 ◽  
Vol 9 (11) ◽  
pp. 1288-1296 ◽  
Author(s):  
Wei Liao ◽  
Dustin E Schones ◽  
Jangsuk Oh ◽  
Yongzhi Cui ◽  
Kairong Cui ◽  
...  

2000 ◽  
Vol 191 (11) ◽  
pp. 1869-1880 ◽  
Author(s):  
Masakatsu Yamashita ◽  
Makoto Katsumata ◽  
Makio Iwashima ◽  
Motoko Kimura ◽  
Chiori Shimizu ◽  
...  

The activation of downstream signaling pathways of both T cell receptor (TCR) and interleukin 4 receptor (IL-4R) is essential for T helper type 2 (Th2) cell development, which is central to understanding immune responses against helminthic parasites and in allergic and autoimmune diseases. However, little is known about how these two distinct signaling pathways cooperate with each other to induce Th2 cells. Here, we show that successful Th2 cell development depends on the effectiveness of TCR-induced activation of calcineurin. An inhibitor of calcineurin activation, FK506, inhibited the in vitro anti-TCR–induced Th2 cell generation in a dose-dependent manner. Furthermore, the development of Th2 cells was significantly impaired in naive T cells from dominant-negative calcineurin Aα transgenic mice, whereas that of Th1 cells was less affected. Efficient calcineurin activation in naive T cells upregulated Janus kinase (Jak)3 transcription and the amount of protein. The generation of Th2 cells induced in vitro by anti-TCR stimulation was inhibited significantly by the presence of Jak3 antisense oligonucleotides, suggesting that the Jak3 upregulation is an important event for the Th2 cell development. Interestingly, signal transducer and activator of transcription (STAT)5 became physically and functionally associated with the IL-4R in the anti-TCR–activated developing Th2 cells that received efficient calcineurin activation, and also in established cloned Th2 cells. In either cell population, the inhibition of STAT5 activation resulted in a diminished IL-4–induced proliferation. Moreover, our results suggest that IL-4–induced STAT5 activation is required for the expansion process of developing Th2 cells. Thus, Th2 cell development is controlled by TCR-mediated activation of the Ca2+/calcineurin pathway, at least in part, by modifying the functional structure of the IL-4R signaling complex.


2018 ◽  
Vol 93 (6) ◽  
pp. 1344-1355 ◽  
Author(s):  
Jonatan Barrera-Chimal ◽  
Gabriel R. Estrela ◽  
Sebastian M. Lechner ◽  
Sébastien Giraud ◽  
Soumaya El Moghrabi ◽  
...  

2007 ◽  
Vol 8 (10) ◽  
pp. 1067-1075 ◽  
Author(s):  
Yoshihiko Tanaka ◽  
Shinjiro Hamano ◽  
Kazuhito Gotoh ◽  
Yuzo Murata ◽  
Yuya Kunisaki ◽  
...  

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