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The novel role of Yin Yang 1 in the acute rejection of liver allografts by activating dendritic cells
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Acute rejection that causes liver transplant dysfunction is the most
common cause of mortality following liver transplantation. The potential
role of Yin Yang 1 (YY1), a widely expressed zinc finger DNA-binding
transcription factor, in acute rejection of liver allografts remains
unknown. Here, we evaluated the effects and mechanisms of YY1 in an
acute rejection using major histocompatibility complex (MHC) class
II-mismatched rat liver transplantation model. On days 5 and 10 after
liver transplantation, allografts showed elevated expression of YY1 in
infiltrating inflammatory cells around the central vein of recipient
livers accompanied by elevated levels of serum transaminase and
proinflammatory cytokines. In vitro analysis showed that
YY1-overexpressing DCs had higher expression of CD80, CD86, and MHC
class II compared with the control group. Additionally,
YY1-overexpressing DCs triggered naïve CD4+ T cells to produce high
levels of intracellular cytokines IL-17 and TNF-γ. These results suggest
that YY1 activates DCs and participates in the pathogenesis of acute
rejection by polarizing naïve T cells to the inflammatory phenotype,
making YY1 a candidate therapeutic target to avoid acute rejection after
liver transplantation.
Title: The novel role of Yin Yang 1 in the acute rejection of liver allografts by activating dendritic cells
Description:
Acute rejection that causes liver transplant dysfunction is the most
common cause of mortality following liver transplantation.
The potential
role of Yin Yang 1 (YY1), a widely expressed zinc finger DNA-binding
transcription factor, in acute rejection of liver allografts remains
unknown.
Here, we evaluated the effects and mechanisms of YY1 in an
acute rejection using major histocompatibility complex (MHC) class
II-mismatched rat liver transplantation model.
On days 5 and 10 after
liver transplantation, allografts showed elevated expression of YY1 in
infiltrating inflammatory cells around the central vein of recipient
livers accompanied by elevated levels of serum transaminase and
proinflammatory cytokines.
In vitro analysis showed that
YY1-overexpressing DCs had higher expression of CD80, CD86, and MHC
class II compared with the control group.
Additionally,
YY1-overexpressing DCs triggered naïve CD4+ T cells to produce high
levels of intracellular cytokines IL-17 and TNF-γ.
These results suggest
that YY1 activates DCs and participates in the pathogenesis of acute
rejection by polarizing naïve T cells to the inflammatory phenotype,
making YY1 a candidate therapeutic target to avoid acute rejection after
liver transplantation.
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