A unique lymphotoxin α,β-dependent pathway regulates thymic emigration of Vα14 invariant natural killer T cells

被引:31
作者
Franki, Ann Sophie
Van Beneden, Katrien
Dewint, Pieter
Hammond, Kirsten J. L.
Lambrecht, Stijn
Leclercq, Georges
Kronenberg, Mitchell
Deforce, Dieter
Elewaut, Dirk
机构
[1] Ghent Univ Hosp, Dept Rheumatol, Lab Mol Immunol & Inflammat, B-9000 Ghent, Belgium
[2] Ghent Univ Hosp, Dept Clin Chem Microbiol & Immunol, B-9000 Ghent, Belgium
[3] Univ Ghent, Fac Pharmaceut Sci, Lab Pharmaceut Biotechnol, B-9000 Ghent, Belgium
[4] La Jolla Inst Allergy & Immunol, Div Dev Immunol, San Diego, CA 92121 USA
关键词
innate immunity; TNF cytokines; development; LT beta R;
D O I
10.1073/pnas.0508892103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Natural killer (NK) T cells using an invariant V alpha 14 (V alpha 14i) T cell receptor rearrangement form a distinct immunoregulatory T cell lineage. Several studies indicated that a NK1.1(-) V alpha 14i NKT precursor cell differentiates and expands within the thymus before export to the peripheral tissues occurs. However, little is known about the signals that cause the emigration of V alpha 14i NKT cells from the thymus to the periphery. Here we show that signaling of lymphotoxin (LT) alpha beta through the LT beta receptor (LT beta R) is indispensable for regulating peripheral but not thymic V alpha 14i NKT cell numbers. Homing to and homeostatic proliferation of thymic V alpha 14i NKT cells in peripheral organs, however, was not dependent on LT beta R. Instead, our data indicate that a LT beta R-expressing thymic stromal cell regulates the thymic emigration of V alpha 14i NKT cells but not conventional T cell receptor alpha beta cells.
引用
收藏
页码:9160 / 9165
页数:6
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