P.2.d.029 Serum matrix metalloproteinase-9 (MMP-9) and interferon gamma (IFN-γ) in bipolar mood disorder

2013 ◽  
Vol 23 ◽  
pp. S380-S381
Author(s):  
A. Remlinger-Molenda ◽  
A. Czech-Kucharska ◽  
M. Wojcicka ◽  
M. Michalak ◽  
J. Losy ◽  
...  
2009 ◽  
Vol 11 (2) ◽  
pp. 128-132 ◽  
Author(s):  
Janusz K. Rybakowski ◽  
Maria Skibinska ◽  
Anna Leszczynska-Rodziewicz ◽  
Leszek Kaczmarek ◽  
Joanna Hauser

2018 ◽  
Vol In Press (In Press) ◽  
Author(s):  
Elham Sadat Mousavi ◽  
Mohammad Reza Asad ◽  
Ali Barzegari ◽  
Mahbobeh Gholizadeh Ahangari

Cytokine ◽  
2011 ◽  
Vol 56 (1) ◽  
pp. 23
Author(s):  
Sujata Balasubramanian ◽  
Meiyun Fan ◽  
Angela F. Messmer-Blust ◽  
Chuan H. Yang ◽  
Lawrence M. Pfeffer ◽  
...  

2011 ◽  
Vol 286 (22) ◽  
pp. 20054-20064 ◽  
Author(s):  
Sujata Balasubramanian ◽  
Meiyun Fan ◽  
Angela F. Messmer-Blust ◽  
Chuan H. Yang ◽  
Jill A. Trendel ◽  
...  

Matrix metalloproteinase-9 (MMP-9) is important in numerous normal and pathological processes, including the angiogenic switch during tumor development and tumor metastasis. Whereas TNF-α and other cytokines up-regulate MMP-9 expression, interferons (IFNs) inhibit MMP-9 expression. We found that IFN-γ treatment or forced expression of the IFN-induced GTPase, mGBP-2, inhibit TNF-α-induced MMP-9 expression in NIH 3T3 fibroblasts, by inhibiting MMP-9 transcription. The NF-κB transcription factor is required for full induction of MMP-9 by TNF-α. Both IFN-γ and mGBP-2 inhibit the transcription of a NF-κB-dependent reporter construct, suggesting that mGBP-2 inhibits MMP-9 induction via inhibition of NF-κB-mediated transcription. Interestingly, mGBP-2 does not inhibit TNF-α-induced degradation of IκBα or p65/RelA translocation into the nucleus. However, mGBP-2 inhibits p65 binding to a κB oligonucleotide probe in gel shift assays and to the MMP-9 promoter in chromatin immunoprecipitation assays. In addition, TNF-α activation of NF-κB in NIH 3T3 cells is dependent on Rac activation, as evidenced by the inhibition of TNF-α induction of NF-κB-mediated transcription by a dominant inhibitory form of Rac1. A role for Rac in the inhibitory action of mGBP-2 on NF-κB is further shown by the findings that mGBP-2 inhibits TNF-α activation of endogenous Rac and constitutively activate Rac can restore NF-κB transcription in the presence of mGBP-2. This is a novel mechanism by which IFNs can inhibit the cytokine induction of MMP-9 expression.


2009 ◽  
Vol 2009 ◽  
pp. 1-7 ◽  
Author(s):  
Janusz K. Rybakowski

Matrix metalloproteinase-9 (MMP9) has been implicated in numerous somatic illnesses, including cardiovascular disorders and cancer. Recently, MMP9 has been shown to be increasingly important in several aspects of central nervous system activity. Furthermore, a pathogenic role for this enzyme has been suggested in such neuropsychiatric disorders as schizophrenia, bipolar illness, and multiple sclerosis. In this paper, the results of biochemical and molecular-genetic studies on MMP9 that have been performed in these pathological conditions will be summarized. Furthermore, I hypothesize that the MMP9 gene, as shown by functional −1562 C/T polymorphism studies, may be mediating the relationship of neuropsychiatric illnesses (schizophrenia, bipolar mood disorder, multiple sclerosis) that are comorbid with cardiovascular disease and cancer.


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