TY - JOUR
T1 - In vivo blockade of T cell development reveals alternative pathways for generation of intraepithelial lymphocytes in mice
AU - Mondoon, Surenchimeg
AU - Shibata, Kensuke
AU - Yoshikai, Yasunobu
N1 - Funding Information:
We thank Yumiko Kitada, Yoshiko Kurisaki and Akiko Yano for their secretarial assistance. This work was supported by Grant-in-Aid for Scientific Research on Innovative Areas JSPS KAKENHI Grant Number JP 16H06496 , Grant-in-Aid for Scientific Research B JSPS KAKENHI Grant Number JP 26293098 (Y.Y) and Grant-in-Aid for Scientific Research C JSPS KAKENHI Grant Number JP 16K08740 (K.S).
Publisher Copyright:
© 2017 European Federation of Immunological Societies
PY - 2017/11
Y1 - 2017/11
N2 - Intraepithelial lymphocytes (IELs) are resident cells localized within the intestinal epithelia and play an important role in regulating gut inflammations and host defense against pathogens. CD8α+ TCRαβ+ IELs are heterogeneous populations that are generated from T cell precursors including CD4− CD8α− double-negative (DN) cells and CD4+ CD8α+ double-positive (DP) cells. However, developmental pathways of TCRαβ+ IELs remained unclear. To gain insight into the mechanisms, we generated mice (Bcl11bΔDN2 mice) that lack thymic precursors (DN CD5+ TCRβ+ cells) for CD4− CD8αα+ TCRαβ+ IELs. Unexpectedly, we found that, in the absence of the precursors in thymi of Bcl11bΔDN2 mice, CD4− CD8αα+ TCRαβ+ IELs were still present in the intestine though the number was reduced. Adoptive transfer experiment showed that their precursors were highly enriched in CD8α+ TCRβ− thymocytes. The CD4− CD8αα+ TCRαβ+ IELs in Bcl11bΔDN2 mice are distinguished by Thy1.2 expression and are indeed present in WT mice. Taken together, our study reveal a novel developmental pathway for CD8αα+ TCRαβ+ IELs.
AB - Intraepithelial lymphocytes (IELs) are resident cells localized within the intestinal epithelia and play an important role in regulating gut inflammations and host defense against pathogens. CD8α+ TCRαβ+ IELs are heterogeneous populations that are generated from T cell precursors including CD4− CD8α− double-negative (DN) cells and CD4+ CD8α+ double-positive (DP) cells. However, developmental pathways of TCRαβ+ IELs remained unclear. To gain insight into the mechanisms, we generated mice (Bcl11bΔDN2 mice) that lack thymic precursors (DN CD5+ TCRβ+ cells) for CD4− CD8αα+ TCRαβ+ IELs. Unexpectedly, we found that, in the absence of the precursors in thymi of Bcl11bΔDN2 mice, CD4− CD8αα+ TCRαβ+ IELs were still present in the intestine though the number was reduced. Adoptive transfer experiment showed that their precursors were highly enriched in CD8α+ TCRβ− thymocytes. The CD4− CD8αα+ TCRαβ+ IELs in Bcl11bΔDN2 mice are distinguished by Thy1.2 expression and are indeed present in WT mice. Taken together, our study reveal a novel developmental pathway for CD8αα+ TCRαβ+ IELs.
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U2 - 10.1016/j.imlet.2017.09.008
DO - 10.1016/j.imlet.2017.09.008
M3 - Article
C2 - 28958836
AN - SCOPUS:85030316009
SN - 0165-2478
VL - 191
SP - 40
EP - 46
JO - Immunology Letters
JF - Immunology Letters
ER -