CD40 expression in HCV-associated chronic liver diseases
CD40 is expressed primarily on B cells and plays an important role in antigen presentation, B cell proliferation, and T cell activation. It has been reported that the CD40 signal modulates apoptosis and has an anti-viral effect in certain cells. Therefore, we investigated the expression and the func...
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Veröffentlicht in: | International journal of molecular medicine 2006-10, Vol.18 (4), p.559-563 |
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Sprache: | eng |
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Zusammenfassung: | CD40 is expressed primarily on B cells and plays an important role in antigen
presentation, B cell proliferation, and T cell activation. It has been reported
that the CD40 signal modulates apoptosis and has an anti-viral effect in certain
cells. Therefore, we investigated the expression and the function of CD40 in HCV-associated
chronic liver disease. The expression of CD40 on liver tissues was determined
through immunohistochemistry on 50 liver specimens obtained from HCV-positive
patients. The effect of CD40 signaling on apoptosis of HepG2 cells was assessed
using the MTT assay. The effect of CD40 stimulation on NF-κB activation was determined
in NF-κB reporter gene-transfected HepG2 cells with the Luciferase assay. CD40
positive hepatocytes were observed in both periportal and lobular areas, accompanied
by inflammation. In both areas, CD40 staining intensity became significantly stronger,
correlating with the histological grading. Similarly, it became stronger with
the progression of the histological staging in F1, F2 and F3 cases; however, the
expression level decreased in F4 cases. CD40 ligation induced apoptosis in HepG2
cells in the presence of 500 ng/ml of actinomycin D, while CD40 ligation alone
could not. Anti-CD40 monoclonal antibody caused NF-κB activation in HepG2 cells
in a dose-dependent manner. These results suggest that hepatocyte over-expression
of CD40 might play an important role in regulating hepatocyte survival and death
in HCV-associated chronic liver diseases. |
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ISSN: | 1107-3756 1791-244X |
DOI: | 10.3892/ijmm.18.4.559 |