TY - JOUR
T1 - Mouse thymic epithelial cell lines expressing "Aire" and peripheral tissue-specific antigens reproduce in vitro negative selection of T cells
AU - Yamaguchi, Yoshitaka
AU - Takayanagi, Atsushi
AU - Chen, Jiabing
AU - Sakai, Kosuke
AU - Kudoh, Jun
AU - Shimizu, Nobuyoshi
N1 - Funding Information:
We thank Drs Setsuko Noda, Shinsei Minoshima and Kenji Tani for valuable technical advice and helpful discussion. This work was supported in part by a Fund for “Research for the Future” Program from the Japan Society for the Promotion of Science (JSPS) to N. S., Grant-in-Aid for Young Scientists B from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) to Y. Y., the 21st Century COE Program and Global COE Program at Keio University to J. K. The authors thank a generous support from Toagosei Co., Ltd, Japan.
PY - 2011/8/15
Y1 - 2011/8/15
N2 - In the human thymus, AIRE (autoimmune regulator) gene is expressed in a very limited type of medullary thymic epithelial cells (mTECs) and no cognate cell lines are available, hence the molecular analysis of AIRE gene function has been difficult. To improve this situation, we attempted to isolate Aire-expressing cells and established three cell lines (Aire+TEC1, Aire+TEC2, Aire+DC) from the abnormally enlarged thymus, which was developed in the transgenic mice expressing SV40 T-antigen driven by the mouse Aire gene promoter. When these Aire+ cell lines were co-cultured with fresh thymocytes, they adhered to the majority of thymocytes and induced apoptosis as if negative selection of T-cells in the thymus is occurring in vitro. Further analysis revealed that these Aire+ cell lines are derived from mTECs and exhibit characteristic natures of "antigen presenting cells" including several distinct abilities: to express a variety of peripheral tissue-specific antigens, to produce immunoproteasome and immunological synapse, and to express some of TNFSFs (tumor necrosis factor super families). Thus, the newly established Aire+ cell lines will be invaluable for the further detailed analysis of AIRE gene function in the central tolerance of immunity and autoimmune disease.
AB - In the human thymus, AIRE (autoimmune regulator) gene is expressed in a very limited type of medullary thymic epithelial cells (mTECs) and no cognate cell lines are available, hence the molecular analysis of AIRE gene function has been difficult. To improve this situation, we attempted to isolate Aire-expressing cells and established three cell lines (Aire+TEC1, Aire+TEC2, Aire+DC) from the abnormally enlarged thymus, which was developed in the transgenic mice expressing SV40 T-antigen driven by the mouse Aire gene promoter. When these Aire+ cell lines were co-cultured with fresh thymocytes, they adhered to the majority of thymocytes and induced apoptosis as if negative selection of T-cells in the thymus is occurring in vitro. Further analysis revealed that these Aire+ cell lines are derived from mTECs and exhibit characteristic natures of "antigen presenting cells" including several distinct abilities: to express a variety of peripheral tissue-specific antigens, to produce immunoproteasome and immunological synapse, and to express some of TNFSFs (tumor necrosis factor super families). Thus, the newly established Aire+ cell lines will be invaluable for the further detailed analysis of AIRE gene function in the central tolerance of immunity and autoimmune disease.
KW - AIRE
KW - Negative selection
KW - Thymocytes and apoptosis
KW - Tolerance
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U2 - 10.1016/j.yexcr.2011.05.002
DO - 10.1016/j.yexcr.2011.05.002
M3 - Article
C2 - 21683072
AN - SCOPUS:79960085650
SN - 0014-4827
VL - 317
SP - 2019
EP - 2030
JO - Experimental Cell Research
JF - Experimental Cell Research
IS - 14
ER -