Hassall's corpuscles with cellular-senescence features maintain IFNα production through neutrophils and pDC activation in the thymus.
Hassall's corpuscles with cellular-senescence features maintain IFNα production through neutrophils and pDC activation in the thymus.
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DOI:
10.1093/intimm/dxy073
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发表时间:
2019-03-05
影响因子:
4.4
通讯作者:
Hamazaki, Yoko
中科院分区:
文献类型:
--
作者:
Wang, Jianwei;Sekai, Miho;Matsui, Takeshi;Fujii, Yosuke;Matsumoto, Mitsuru;Takeuchi, Osamu;Minato, Nagahiro;Hamazaki, Yoko
Hassall’s corpuscles activate neutrophils to stimulate pDCs in the thymus Hassall’s corpuscles (HCs) are composed of cornifying, terminally differentiated medullary thymic epithelial cells (mTECs) that are developed under the control of Aire. Here, we demonstrated that HC-mTECs show features of cellular senescence and produce inflammatory cytokines and chemokines including CXCL5, thereby recruiting and activating neutrophils to produce IL-23 in the thymic medulla. We further indicated that thymic plasmacytoid dendritic cells (pDCs) expressing IL-23 receptors constitutively produced Ifna, which plays a role in single positive (SP) cell maturation, in an Il23a-dependent manner. Neutrophil depletion with anti-Ly6G antibody injection resulted in a significant decrease of Ifna expression in the thymic pDCs, suggesting that thymic neutrophil activation underlies the Ifna expression in thymic pDCs in steady state conditions. A New Zealand White mouse strain showing HC hyperplasia exhibited greater numbers and activation of thymic neutrophils and pDCs than B6 mice, whereas Aire-deficient B6 mice with defective HC development and SP thymocyte maturation showed significantly compromised numbers and activation of these cells. These results collectively suggested that HC-mTECs with cell-senescence features initiate a unique cell activation cascade including neutrophils and pDCs leading to the constitutive IFNα expression required for SP T-cell maturation in the thymic medulla.
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DOI:
10.1126/science.1218004
发表时间:
2012-04-06
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Dudakov JA;Hanash AM;Jenq RR;Young LF;Ghosh A;Singer NV;West ML;Smith OM;Holland AM;Tsai JJ;Boyd RL;van den Brink MR
通讯作者:
van den Brink MR
DOI:
10.4049/jimmunol.0804133
发表时间:
2009-12-15
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Laan M;Kisand K;Kont V;Möll K;Tserel L;Scott HS;Peterson P
通讯作者:
Peterson P
DOI:
10.1111/nyas.12960
发表时间:
2015-01-01
期刊:
YEAR IN IMMUNOLOGY
影响因子:
--
作者:
Chan, Alice Y.;Anderson, Mark S.
通讯作者:
Anderson, Mark S.
影响因子:
10.5
作者:
Chien, Yuchen;Scuoppo, Claudio;Lowe, Scott W.
通讯作者:
Lowe, Scott W.
影响因子:
29.4
作者:
Dobes, Jan;Neuwirth, Ales;Filipp, Dominik
通讯作者:
Filipp, Dominik