Intensive generation of NK1.1(-) extrathymic T cells in the liver by injection of bone marrow cells isolated from mice with a mutation of polymorphicmajor histocompatibility complex antigens
Rc. Halder et al., Intensive generation of NK1.1(-) extrathymic T cells in the liver by injection of bone marrow cells isolated from mice with a mutation of polymorphicmajor histocompatibility complex antigens, IMMUNOLOGY, 102(4), 2001, pp. 450-459
Whether intermediate TCR (TCRint) cells and natural killer T (NKT or NK1.1(
+)TCR(int)) cells are extrathymically generated remains controversial. This
arises from the fact that there are few of these T cells in the athymic nu
de mice and neonatally thymectomized mice. However, when athymic mice were
provided with appropriate microenvironments or stimulation, many TCRint cel
ls (mainly NK1.1(-)) were found to arise in the liver. NKT cells are known
to be positively selected by monomorphic major histocompatibility complex (
MHD)-like antigens (e.g. CD1d). This is true even if they are CD4(+). In ot
her words, a MHC class 1-like antigen is restricted to CD4 antigen. This ru
le is somewhat different from that seen in conventional T cells (i.e., the
restriction of class II with CD4 and that of class I and CD8). In the case
of NK1.1(-)TCR(int) cells, they were selected by polymorphic MHC antigens,
but their MHC restriction to CD4 or CD8 antigen was incomplete. This was re
vealed by experiments of bone marrow transfer with class I (bm 1) or II (bm
12) disparity. Depending on the disparity, a unique cytokine profile in se
ra was detected. These results suggest that the development of T lineage ly
mphocytes and MHC restriction to CD4 and CD8 might have occurred in paralle
l as a phylogenic event, and that NK1.1(-) extrathymic T cells (i.e., NK1.1
(-)TCR(int)) are at an intermediate position between NKT cells and conventi
onal T cells in phylogeny.