| Literature DB >> 14764670 |
Luqiu Chen1, Kristy A Grabowski, Jun-Ping Xin, John Coleman, Zan Huang, Baltazar Espiritu, Serhan Alkan, H Bill Xie, Yuechun Zhu, Fletcher A White, John Clancy, Hua Huang.
Abstract
Innate effector cells that produce Th2-type cytokines are critical in Th2 cell-mediated immune responses. However, it is not known how these cells acquire the ability to produce Th2 cytokines. IL-4 is a potent inducer that directs differentiation of naive CD4(+) T cells into CD4(+) Th2 effector cells. To determine whether IL-4 can induce differentiation and expansion of Th2 cytokine-producing innate cells, we used mice whose il-4 gene was replaced by a knock-in green fluorescence protein (gfp) gene. We found that, directly ex vivo, IL-4 increased the number of GFP(+) cells in the airway and the lung tissue in an Ag-specific manner. The majority of GFP(+) cells were eosinophils, suggesting that IL-4 plays a pivotal role in expanding IL-4-producing eosinophils in vivo. IL-4-producing eosinophils showed some unique features compared with IL-4-producing CD4(+) T cells. They exhibited biallelic expression of the il-4 gene when stimulated and were more dominant IL-4- and IL-5-producing cells. Furthermore, we show that IL-4 drove bone marrow progenitor cells to differentiate into Th2 cytokine-producing eosinophils in vitro. These results strongly suggest IL-4 is a potent factor in directing bone marrow progenitor cells to differentiate into Th2 cytokine-producing eosinophils.Entities:
Mesh:
Substances:
Year: 2004 PMID: 14764670 DOI: 10.4049/jimmunol.172.4.2059
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422