KMID : 0578320120330030259
|
|
Molecules and Cells 2012 Volume.33 No. 3 p.259 ~ p.267
|
|
CD99-Dependent Expansion of Myeloid-Derived Suppressor Cells and Attenuation of Graft-Versus-Host Disease
|
|
Park Hyo-Jin
Byun Da-Hye Lee An-Hi Kim Ju-Hyun Ban Young-Larn Masatake Araki Kimi Araki Ken-ichi Yamamura Kim In-Ho Park Seong-Hoe Jung Kyeong-Cheon
|
|
Abstract
|
|
|
CD99 is involved in many cellular events, such as the generation of Hodgkin and Reed-Sternberg cells, T cell co-stimulation, and leukocyte transendothelial migration. However, these studies have been limited to in vitro or in vivo experiments using CD99-deficient cell lines or anti-CD99 antibodies. In the present study, using CD99-deficient mice established by the exchangeable gene trap method, we investigated the physiologic function of murine CD99. In a B6 splenocytes ? bm12 graft-versus-host disease model, wild-type cells were minimally lethal, whereas all mice that received CD99-deficient donor cells developed an early and more severe pathology. Graft-versus-host disease in these mice was associated with insufficient expansion of myeloid-derived suppressor cells. This was confirmed by experiments illustrating that the injection of wild-type donor cells depleted of Mac-1+ cells led to an almost identical disease course as the CD99-deficient donor system. Therefore, these results suggest that CD99 plays a crucial role in the attenuation of graft-versus-host disease by regulating the expansion of myeloid-derived suppressor cells.
|
|
KEYWORD
|
|
CD99, graft versus host disease, myeloid cells
|
|
FullTexts / Linksout information
|
|
|
|
Listed journal information
|
|
|