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dc.contributor.authorMerzaban, Jasmeen
dc.contributor.authorBurdick, Monica M.
dc.contributor.authorGadhoum, Samah
dc.contributor.authorDagia, Nilesh M.
dc.contributor.authorChu, Julia T.
dc.contributor.authorFuhlbrigge, Robert C.
dc.contributor.authorSackstein, Robert D.
dc.date.accessioned2015-08-12T08:56:37Z
dc.date.available2015-08-12T08:56:37Z
dc.date.issued2011-06-09
dc.identifier.issn00064971
dc.identifier.pmid21659548
dc.identifier.doi10.1182/blood-2010-11-320705
dc.identifier.urihttp://hdl.handle.net/10754/565953
dc.description.abstractAlthough well recognized that expression of E-selectin on marrow microvessels mediates osteotropism of hematopoietic stem/progenitor cells (HSPCs), our knowledge regarding the cognate E-selectin ligand(s) on HSPCs is incomplete. Flow cytometry using E-selectin-Ig chimera (E-Ig) shows that human marrow cells enriched for HSPCs (CD34+ cells) display greater E-selectin binding than those obtained from mouse (lin-/Sca-1+/c-kit+ [LSK] cells). To define the relevant glycoprotein E-selectin ligands, lysates from human CD34+ and KG1a cells and from mouse LSK cells were immunoprecipitated using E-Ig and resolved byWestern blot using E-Ig. In both human and mouse cells, E-selectin ligand reactivity was observed at ∼ 120- to 130-kDa region, which contained two E-selectin ligands, the P-selectin glycoprotein ligand- 1 glycoform "CLA," and CD43. Human, but not mouse, cells displayed a prominent ∼ 100-kDa band, exclusively comprising the CD44 glycoform "HCELL."E-Ig reactivity was most prominent on CLA in mouse cells and on HCELL in human cells. To further assess HCELL's contribution to E-selectin adherence, complementary studies were performed to silence (via CD44 siRNA) or enforce its expression (via exoglycosylation). Under physiologic shear conditions, CD44/HCELL-silenced human cells showed striking decreases (> 50%) in E-selectin binding. Conversely, enforced HCELL expression of LSK cells profoundly increased E-selectin adherence, yielding > 3-fold more marrow homing in vivo. These data define the key glycoprotein E-selectin ligands of human and mouse HSPCs, unveiling critical species-intrinsic differences in both the identity and activity of these structures. © 2011 by The American Society of Hematology.
dc.publisherAmerican Society of Hematology
dc.titleAnalysis of glycoprotein E-selectin ligANDs on human and mouse marrow cells enriched for hematopoietic stem/progenitor cells
dc.typeArticle
dc.contributor.departmentBiological and Environmental Sciences and Engineering (BESE) Division
dc.contributor.departmentBioscience Program
dc.identifier.journalBlood
dc.identifier.pmcidPMC3158712
kaust.personMerzaban, Jasmeen S.
kaust.personGadhoum, Samah
dc.date.published-online2011-06-09
dc.date.published-print2011-08-18


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