AbstractS100A8, S100A9 and S100A12 proteins are associated with inflammation and tissue remodelling, both processes known to be associated with high protease activity. Here, we report that homo-oligomeric forms of S100A8 and S100A9 are readily degraded by proteases, but that the preferred hetero-oligomeric S100A8/A9 complex displays a high resistance even against proteinase K degradation. S100A12 is not as protease resistant as the S100A8/A9 complex. Since specific functions have been assigned to the homo- and heterooligomeric forms of the S100A8 and A9 proteins, this finding may point to a post-translational level of regulation of the various functions of these proteins in inflammation and tissue remodelling
S100A8, S100A9 and S100A12 are generally considered pro-inflammatory proteins because their expressi...
<div><p>(A) Control and S100A14 over-expressing CaLH3 cells were treated with protein synthesis inhi...
Autoimmune diseases, such as psoriasis and arthritis, show a patchy distribution of inflammation des...
AbstractS100A8, S100A9 and S100A12 proteins are associated with inflammation and tissue remodelling,...
<div><p>S100A8 and S100A9 are Ca<sup>2+</sup>-binding proteins that are associated with acute and ch...
S100A8 and S100A9 are Ca2+-binding proteins that are associated with acute and chronic inflammation ...
S100A8 and S100A9 are Ca(2+)-binding proteins that are associated with acute and chronic inflammatio...
S100A8 and S100A9 are Ca(2+)-binding proteins that are associated with acute and chronic inflammatio...
Several S100 Ca²⁺-binding proteins undergo various post-translational modifications that may alter t...
We show here that increased S100A8 and S100A9 protein expression is induced in spleen of animals wit...
Upon tissue injury and infection both stressed and dying cells can release proteins that normally re...
The functional importance of members of the S100 Ca-binding protein family is recently emerging. A v...
Several S100 Ca2-binding proteins undergo various post-translational modifications that may alter th...
S100A8 and S100A9 (also known as MRP8 and MRP14, respectively) are Ca2+ binding proteins belonging t...
Inflammation, insoluble protein deposition and neuronal cell loss are important features of the Alzh...
S100A8, S100A9 and S100A12 are generally considered pro-inflammatory proteins because their expressi...
<div><p>(A) Control and S100A14 over-expressing CaLH3 cells were treated with protein synthesis inhi...
Autoimmune diseases, such as psoriasis and arthritis, show a patchy distribution of inflammation des...
AbstractS100A8, S100A9 and S100A12 proteins are associated with inflammation and tissue remodelling,...
<div><p>S100A8 and S100A9 are Ca<sup>2+</sup>-binding proteins that are associated with acute and ch...
S100A8 and S100A9 are Ca2+-binding proteins that are associated with acute and chronic inflammation ...
S100A8 and S100A9 are Ca(2+)-binding proteins that are associated with acute and chronic inflammatio...
S100A8 and S100A9 are Ca(2+)-binding proteins that are associated with acute and chronic inflammatio...
Several S100 Ca²⁺-binding proteins undergo various post-translational modifications that may alter t...
We show here that increased S100A8 and S100A9 protein expression is induced in spleen of animals wit...
Upon tissue injury and infection both stressed and dying cells can release proteins that normally re...
The functional importance of members of the S100 Ca-binding protein family is recently emerging. A v...
Several S100 Ca2-binding proteins undergo various post-translational modifications that may alter th...
S100A8 and S100A9 (also known as MRP8 and MRP14, respectively) are Ca2+ binding proteins belonging t...
Inflammation, insoluble protein deposition and neuronal cell loss are important features of the Alzh...
S100A8, S100A9 and S100A12 are generally considered pro-inflammatory proteins because their expressi...
<div><p>(A) Control and S100A14 over-expressing CaLH3 cells were treated with protein synthesis inhi...
Autoimmune diseases, such as psoriasis and arthritis, show a patchy distribution of inflammation des...