TY - JOUR
T1 - The outsiders
T2 - Emerging roles of ectonucleotidases in inflammation
AU - Szabo, Csaba
AU - Pacher, Pal
PY - 2012/8/8
Y1 - 2012/8/8
N2 - Research on the biological roles of ectonucleoidases has revealed that CD73, an ecto-5′ nucleotidase, plays a special role in the extracellular conversion of adenosine monophosphate to adenosine - specifically, as a checkpoint that determines whether the extracellular environment is proinflammatory (characterized by adenosine 5′-triphosphate-mediated responses) or anti-inflammatory (adenosine-mediated responses). Inactivating or inhibiting CD73 attenuates the extracellular formation of adenosine, exacerbating the severity of various inflammatory diseases. In this issue of Science Translational Medicine, Flögel and colleagues showed that CD73 can be pharmacologically exploited to convert an inactive adenosine precursor to an active, anti-inflammatory adenosine analog. In addition to attenuating inflammation associated with collagen-induced arthritis in a mouse model, this prodrug approach was site-selective, because the metabolic conversion relies on CD73, which is up-regulated in the inflammatory locus (the joint).
AB - Research on the biological roles of ectonucleoidases has revealed that CD73, an ecto-5′ nucleotidase, plays a special role in the extracellular conversion of adenosine monophosphate to adenosine - specifically, as a checkpoint that determines whether the extracellular environment is proinflammatory (characterized by adenosine 5′-triphosphate-mediated responses) or anti-inflammatory (adenosine-mediated responses). Inactivating or inhibiting CD73 attenuates the extracellular formation of adenosine, exacerbating the severity of various inflammatory diseases. In this issue of Science Translational Medicine, Flögel and colleagues showed that CD73 can be pharmacologically exploited to convert an inactive adenosine precursor to an active, anti-inflammatory adenosine analog. In addition to attenuating inflammation associated with collagen-induced arthritis in a mouse model, this prodrug approach was site-selective, because the metabolic conversion relies on CD73, which is up-regulated in the inflammatory locus (the joint).
UR - http://www.scopus.com/inward/record.url?scp=84864880288&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84864880288&partnerID=8YFLogxK
U2 - 10.1126/scitranslmed.3004378
DO - 10.1126/scitranslmed.3004378
M3 - Review article
C2 - 22875826
AN - SCOPUS:84864880288
SN - 1946-6234
VL - 4
JO - Science Translational Medicine
JF - Science Translational Medicine
IS - 146
M1 - 146ps14
ER -