TY - JOUR
T1 - Neuropilin 1 is expressed on thymus-derived natural regulatory T cells, but not mucosagenerated induced Foxp3+ T reg cells
AU - Weiss, Jonathan M.
AU - Bilate, Angelina M.
AU - Gobert, Michael
AU - Ding, Yi
AU - de Lafaille, Maria A.Curotto
AU - Parkhurst, Christopher N.
AU - Xiong, Huizhong
AU - Dolpady, Jayashree
AU - Frey, Alan B.
AU - Ruocco, Maria Grazia
AU - Yang, Yi
AU - Floess, Stefan
AU - Huehn, Jochen
AU - Oh, Soyoung
AU - Li, Ming O.
AU - Niec, Rachel E.
AU - Rudensky, Alexander Y.
AU - Dustin, Michael L.
AU - Littman, Dan R.
AU - Lafaille, Juan J.
PY - 2012/9
Y1 - 2012/9
N2 - Foxp3 activity is essential for the normal function of the immune system. Two types of regulatory T (T reg) cells express Foxp3, thymus-generated natural T reg (nT reg) cells, and peripherally generated adaptive T reg (iT reg) cells. These cell types have complementary functions. Until now, it has not been possible to distinguish iT reg from nT reg cells in vivo based solely on surface markers. We report here that Neuropilin 1 (Nrp1) is expressed at high levels by most nT reg cells; in contrast, mucosa-generated iT reg and other noninflammatory iT reg cells express low levels of Nrp1. We found that Nrp1 expression is under the control of TGF-β. By tracing nT reg and iT reg cells, we could establish that some tumors have a very large proportion of infiltrating iT reg cells. iT reg cells obtained from highly inflammatory environments, such as the spinal cords of mice with spontaneous autoimmune encephalomyelitis (EAE) and the lungs of mice with chronic asthma, express Nrp1. In the same animals, iT reg cells in secondary lymphoid organs remain Nrp1low. We also determined that, in spontaneous EAE, iT reg cells help to establish a chronic phase of the disease.
AB - Foxp3 activity is essential for the normal function of the immune system. Two types of regulatory T (T reg) cells express Foxp3, thymus-generated natural T reg (nT reg) cells, and peripherally generated adaptive T reg (iT reg) cells. These cell types have complementary functions. Until now, it has not been possible to distinguish iT reg from nT reg cells in vivo based solely on surface markers. We report here that Neuropilin 1 (Nrp1) is expressed at high levels by most nT reg cells; in contrast, mucosa-generated iT reg and other noninflammatory iT reg cells express low levels of Nrp1. We found that Nrp1 expression is under the control of TGF-β. By tracing nT reg and iT reg cells, we could establish that some tumors have a very large proportion of infiltrating iT reg cells. iT reg cells obtained from highly inflammatory environments, such as the spinal cords of mice with spontaneous autoimmune encephalomyelitis (EAE) and the lungs of mice with chronic asthma, express Nrp1. In the same animals, iT reg cells in secondary lymphoid organs remain Nrp1low. We also determined that, in spontaneous EAE, iT reg cells help to establish a chronic phase of the disease.
UR - http://www.scopus.com/inward/record.url?scp=84867899425&partnerID=8YFLogxK
U2 - 10.1084/jem.20120914
DO - 10.1084/jem.20120914
M3 - Article
C2 - 22966001
AN - SCOPUS:84867899425
SN - 0022-1007
VL - 209
SP - 1723
EP - 1742
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 10
ER -