[HTML][HTML] Osteopontin attenuates acute gastrointestinal graft-versus-host disease by preventing apoptosis of intestinal epithelial cells
K Kawakami, N Minami, M Matsuura, T Iida… - Biochemical and …, 2017 - Elsevier
K Kawakami, N Minami, M Matsuura, T Iida, T Toyonaga, K Nagaishi, Y Arimura, M Fujimiya…
Biochemical and biophysical research communications, 2017•ElsevierBackground and aims Acute graft-versus-host disease (GVHD) is a major complication after
allogeneic hematopoietic stem cell transplantation, which often targets gastrointestinal (GI)
tract. Osteopontin (OPN) plays an important physiological role in the efficient development of
Th1 immune responses and cell survival by inhibiting apoptosis. The role of OPN in acute GI-
GVHD is poorly understood. In the present study, we investigated the role of OPN in donor T
cells in the pathogenicity of acute GI-GVHD. Methods OPN knockout (KO) mice and C57BL/6 …
allogeneic hematopoietic stem cell transplantation, which often targets gastrointestinal (GI)
tract. Osteopontin (OPN) plays an important physiological role in the efficient development of
Th1 immune responses and cell survival by inhibiting apoptosis. The role of OPN in acute GI-
GVHD is poorly understood. In the present study, we investigated the role of OPN in donor T
cells in the pathogenicity of acute GI-GVHD. Methods OPN knockout (KO) mice and C57BL/6 …
Background and aims
Acute graft-versus-host disease (GVHD) is a major complication after allogeneic hematopoietic stem cell transplantation, which often targets gastrointestinal (GI) tract. Osteopontin (OPN) plays an important physiological role in the efficient development of Th1 immune responses and cell survival by inhibiting apoptosis. The role of OPN in acute GI-GVHD is poorly understood. In the present study, we investigated the role of OPN in donor T cells in the pathogenicity of acute GI-GVHD.
Methods
OPN knockout (KO) mice and C57BL/6 (B6) mice were used as donors, and (C57BL/6 × DBA/2) F1 (BDF1) mice were used as allograft recipients. Mice with acute GI-GVHD were divided into three groups: the control group (BDF1→BDF1), B6 group (B6→BDF1), and OPN-KO group (OPN-KO→BDF1). Bone marrow cells and spleen cells from donors were transplanted to lethally irradiated recipients. Clinical GVHD scores were assessed daily. Recipients were euthanized on day 7 after transplantation, and colons and small intestines were collected for various analyses.
Results
The clinical GVHD score in the OPN-KO group was significantly increased compared with the B6 and control groups. We observed a difference in the severity of colonic GVHD between the OPN-KO group and B6 group, but not small intestinal-GVHD between these groups. Interferon-γ, Tumor necrosis factor-α, Interleukin-17A, and Interleukin-18 gene expression in the OPN-KO group was differed between the colon and small intestine. Flow cytometric analysis revealed that the fluorescence intensity of splenic and colonic CD8 T cells expressing Fas Ligand was increased in the OPN-KO group compared with the B6 group.
Conclusion
We demonstrated that the importance of OPN in T cells in the onset of acute GI-GVHD involves regulating apoptosis of the intestinal cell via the Fas-Fas Ligand pathway.
Elsevier