Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/234956
Title: CD163 and IgG Codefend against Cytotoxic Hemoglobin via Autocrine and Paracrine Mechanisms
Authors: Subramanian, Karthik
Du, Ruijuan 
Tan, Nguan Soon 
Ho, Bow 
Ding, Jeak Ling 
Keywords: Science & Technology
Life Sciences & Biomedicine
Immunology
SCAVENGER RECEPTOR
IN-VIVO
ACTIVATION
MONOCYTES
CELLS
INFLAMMATION
EXPRESSION
INDUCTION
MEMBER
LIVER
Issue Date: 15-May-2013
Publisher: AMER ASSOC IMMUNOLOGISTS
Citation: Subramanian, Karthik, Du, Ruijuan, Tan, Nguan Soon, Ho, Bow, Ding, Jeak Ling (2013-05-15). CD163 and IgG Codefend against Cytotoxic Hemoglobin via Autocrine and Paracrine Mechanisms. JOURNAL OF IMMUNOLOGY 190 (10) : 5267-5278. ScholarBank@NUS Repository.
Abstract: Lysis of RBCs during numerous clinical settings such as severe hemolytic anemia, infection, tissue injury, or blood transfusion releases the endogenous damage-associated molecular pattern, hemoglobin (Hb), into the plasma. The redox-reactive Hb generates cytotoxic reactive oxygen species, disrupting the redox balance and impairing the immune-responsive blood cells. Therefore, it is crucial to understand how the immune system defends against the cytotoxic Hb. We identified a shortcut 'capture and quench' mechanism of detoxification of Hb by the monocyte scavenger receptor CD163, independent of the well-known dominant antioxidant, haptoglobin. Our findings support a highly efficient two-pass mechanism of detoxification and clearance of Hb: 1) a direct suppression of Hb-pseudoperoxidase activity by CD163, involving an autocrine loop of CD163 shedding, sequestration of Hb, recycling, and homeostasis of CD163 in human monocytes and 2) paracrine transactivation of endothelial cells by the shedded soluble CD163 (sCD163), which further detoxifies and clears residual Hb. We showed that sCD163 and IgG interact with free Hb in the plasma and subsequently the sCD163-Hb-IgG complex is endocytosed into monocytes via FcgR. The endocytosed sCD163 is recycled to restore the homeostasis of CD163 on the monocyte membrane in an autocrine cycle, whereas the internalized Hb is catabolized. Using ex vivo coculture experiments, we demonstrated that the monocyte-derived sCD163 and IgG shuttle residual plasma Hb into the proximal endothelial cells. These findings suggest that CD163 and IgG collaborate to engage monocytes and endothelial cells in a two-pass detoxification mechanism to mount a systemic defense against Hb-induced oxidative stress. © 2013 by The American Association of Immunologists, Inc.
Source Title: JOURNAL OF IMMUNOLOGY
URI: https://scholarbank.nus.edu.sg/handle/10635/234956
ISSN: 0022-1767
1550-6606
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