AUTHOR=Zhang Ping , Nguyen Julia , Abdulla Fuad , Nelson Alexander T. , Beckman Joan D. , Vercellotti Gregory M. , Belcher John D. 

TITLE=Soluble MD-2 and Heme in Sickle Cell Disease Plasma Promote Pro-Inflammatory Signaling in Endothelial Cells

JOURNAL=Frontiers in Immunology

VOLUME=Volume 12 - 2021

YEAR=2021

URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2021.632709

DOI=10.3389/fimmu.2021.632709

ISSN=1664-3224

ABSTRACT=Recent evidence indicates that hemolysis in sickle cell disease (SCD) promotes inflammation via innate immune signaling through toll-like receptor 4 (TLR4).  Free heme released by hemolyzed red blood cells can bind to myeloid differentiation factor-2 (MD-2) and activate TLR4 pro-inflammatory signaling on endothelium to promote vaso-occlusion and acute chest syndrome in murine models of SCD. MD-2 is co-expressed with TLR4 on cell membranes, but in inflammatory conditions, soluble MD-2 (sMD-2) is elevated in plasma.  We examined sMD-2 in sickle (SS) plasma and its contribution to pro-inflammatory IL-8 production by endothelial cells. sMD-2 levels were significantly increased in human and murine SS plasma as compared to normal (AA) plasma. Human umbilical vein endothelial cells (HUVEC) exposed to human SS plasma had a 2-fold increase in TLR4-dependent IL-8 secretion as compared to HUEVC exposed to AA plasma. The increase in IL-8 in response to SS plasma was blocked by depletion of sMD-2 from SS plasma, addition of a TLR4 signaling inhibitor TAK-242, or addition of the high-affinity heme-binding protein hemopexin. Similarly, addition of recombinant sMD-2 to AA plasma increased IL-8 secretion. These data suggest that sMD-2 bound to heme might play an important role in pro-inflammatory signaling by endothelium in SCD.