Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-18008
Buehler, P W; Abraham, B; Vallelian, F; Linnemayr, C; Pereira, C P; Cipollo, J F; Jia, Y; Mikolajczyk, M; Boretti, F S; Schoedon, G; Alayash, A I; Schaer, D J (2009). Haptoglobin preserves the CD163 hemoglobin scavenger pathway by shielding hemoglobin from peroxidative modification. Blood, 113(11):2578-2586.
Detoxification and clearance of extracellular hemoglobin (Hb) have been attributed to its removal by the CD163 scavenger receptor pathway. However, even low-level hydrogen peroxide (H(2)O(2)) exposure irreversibly modifies Hb and severely impairs Hb endocytosis by CD163. We show here that when Hb is bound to the high-affinity Hb scavenger protein haptoglobin (Hp), the complex protects Hb from structural modification by preventing alpha-globin cross-links and oxidations of amino acids in critical regions of the beta-globin chain (eg, Trp15, Cys93, and Cys112). As a result of this structural stabilization, H(2)O(2)-exposed Hb-Hp binds to CD163 with the same affinity as nonoxidized complex. Endocytosis and lysosomal translocation of oxidized Hb-Hp by CD163-expressing cells were found to be as efficient as with nonoxidized complex. Hp complex formation did not alter Hb's ability to consume added H(2)O(2) by redox cycling, suggesting that within the complex the oxidative radical burden is shifted to Hp. We provide structural and functional evidence that Hp protects Hb when oxidatively challenged with H(2)O(2) preserving CD163-mediated Hb clearance under oxidative stress conditions. In addition, our data provide in vivo evidence that unbound Hb is oxidatively modified within extravascular compartments consistent with our in vitro findings.
|Item Type:||Journal Article, refereed, original work|
|Communities & Collections:||04 Faculty of Medicine > University Hospital Zurich > Clinic and Policlinic for Internal Medicine|
05 Vetsuisse Faculty > Veterinary Clinic > Department of Small Animals > Clinic for Small Animal Internal Medicine
|DDC:||570 Life sciences; biology|
610 Medicine & health
|Date:||12 March 2009|
|Deposited On:||16 Sep 2009 16:42|
|Last Modified:||27 Nov 2013 22:27|
|Publisher:||American Society of Hematology|
|Additional Information:||This research was originally published in Blood. BLOOD, 12 MARCH 2009 VOLUME 113, NUMBER 11. Copyright by the American Society of Hematology|
|Citations:||Web of Science®. Times cited: 58|
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