Identification of embryonic precursor cells that differentiate into thymic epithelial cells expressing autoimmune regulator

鉴定分化为表达自身免疫调节因子的胸腺上皮细胞的胚胎前体细胞

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作者:Nobuko Akiyama,Nobukazu Takizawa,Maki Miyauchi,Hiromi Yanai,Ryosuke Tateishi,Miho Shinzawa,Riko Yoshinaga,Masaaki Kurihara,Yosuke Demizu,Hisataka Yasuda,Shintaro Yagi,Guoying Wu,Mitsuru Matsumoto,Reiko Sakamoto,Nobuaki Yoshida,Josef M Penninger,Yasuhiro Kobayashi,Jun-Ichiro Inoue,Taishin Akiyama

Abstract

Medullary thymic epithelial cells (mTECs) expressing autoimmune regulator (Aire) are critical for preventing the onset of autoimmunity. However, the differentiation program of Aire-expressing mTECs (Aire(+) mTECs) is unclear. Here, we describe novel embryonic precursors of Aire(+) mTECs. We found the candidate precursors of Aire(+) mTECs (pMECs) by monitoring the expression of receptor activator of nuclear factor-κB (RANK), which is required for Aire(+) mTEC differentiation. pMECs unexpectedly expressed cortical TEC molecules in addition to the mTEC markers UEA-1 ligand and RANK and differentiated into mTECs in reaggregation thymic organ culture. Introduction of pMECs in the embryonic thymus permitted long-term maintenance of Aire(+) mTECs and efficiently suppressed the onset of autoimmunity induced by Aire(+) mTEC deficiency. Mechanistically, pMECs differentiated into Aire(+) mTECs by tumor necrosis factor receptor-associated factor 6-dependent RANK signaling. Moreover, nonclassical nuclear factor-κB activation triggered by RANK and lymphotoxin-β receptor signaling promoted pMEC induction from progenitors exhibiting lower RANK expression and higher CD24 expression. Thus, our findings identified two novel stages in the differentiation program of Aire(+) mTECs.

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