TY - JOUR
T1 - Curriculum vitae of intestinal intraepithelial T cells
T2 - Their developmental and behavioral characteristics
AU - Ishikawa, Hiromichi
AU - Naito, Tomoaki
AU - Iwanaga, Toshihiko
AU - Takahashi-Iwanaga, Hiromi
AU - Suematsu, Makoto
AU - Hibi, Toshifumi
AU - Nanno, Masanobu
PY - 2007/2
Y1 - 2007/2
N2 - The alimentary tract has an epithelial layer, consisting mainly of intestinal epithelial cells (IECs), that is exposed to the exterior world through the intestinal lumen. The IEC layer contains many intestinal intraepithelial T cells (IELs), and the total number of IELs constitutes the largest population in the peripheral T-cell pool. Virtually all γδ-IELs and many αβ-IELs in the mouse small intestine are known to express CD8αα homodimers. A wide range of evidence that supports extrathymic development of these CD8αα+ IELs has been collected. In addition, while several studies identified cells with precursor T-cell phenotypes within the gut epithelium, how these precursors, which are dispersed along the length of the intestine, develop into γδ-IELs and/or αβ-IELs has not been clarified. The identification of lymphoid cell aggregations named 'cryptopatches' (CPs) in the intestinal crypt lamina propria of mice as sites rich in T-cell precursors in 1996 by our research group, however, provided evidence for a central site, whereby precursor IELs could give rise to T-cell receptor-bearing IELs. In this review, we discuss the development of IELs in the intestinal mucosa and examine the possibility that CPs serve as a production site of extrathymic IELs.
AB - The alimentary tract has an epithelial layer, consisting mainly of intestinal epithelial cells (IECs), that is exposed to the exterior world through the intestinal lumen. The IEC layer contains many intestinal intraepithelial T cells (IELs), and the total number of IELs constitutes the largest population in the peripheral T-cell pool. Virtually all γδ-IELs and many αβ-IELs in the mouse small intestine are known to express CD8αα homodimers. A wide range of evidence that supports extrathymic development of these CD8αα+ IELs has been collected. In addition, while several studies identified cells with precursor T-cell phenotypes within the gut epithelium, how these precursors, which are dispersed along the length of the intestine, develop into γδ-IELs and/or αβ-IELs has not been clarified. The identification of lymphoid cell aggregations named 'cryptopatches' (CPs) in the intestinal crypt lamina propria of mice as sites rich in T-cell precursors in 1996 by our research group, however, provided evidence for a central site, whereby precursor IELs could give rise to T-cell receptor-bearing IELs. In this review, we discuss the development of IELs in the intestinal mucosa and examine the possibility that CPs serve as a production site of extrathymic IELs.
KW - CD8αα-IEL
KW - Cryptopatches
KW - Extrathymic development of IEL
KW - αβ-IEL
KW - γδ-IEL
UR - http://www.scopus.com/inward/record.url?scp=33846817326&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33846817326&partnerID=8YFLogxK
U2 - 10.1111/j.1600-065X.2006.00473.x
DO - 10.1111/j.1600-065X.2006.00473.x
M3 - Review article
C2 - 17291286
AN - SCOPUS:33846817326
SN - 0105-2896
VL - 215
SP - 154
EP - 165
JO - Immunological Reviews
JF - Immunological Reviews
IS - 1
ER -