1. Academic Validation
  2. Characterization of CD33 as a new member of the sialoadhesin family of cellular interaction molecules

Characterization of CD33 as a new member of the sialoadhesin family of cellular interaction molecules

  • Blood. 1995 Apr 15;85(8):2005-12.
S D Freeman 1 S Kelm E K Barber P R Crocker
Affiliations

Affiliation

  • 1 Molecular Haemopoiesis Laboratory, Imperial Cancer Research Fund (ICRF), University of Oxford, John Radcliffe Hospital, Headington, UK.
PMID: 7718872
Abstract

CD33 is a member of the Ig superfamily that is restricted to cells of the myelomonocytic lineage but whose functions and binding properties are unknown. It shares sequence similarity with sialoadhesin, CD22, and the myelin-associated glycoprotein, which constitute the Sialoadhesin family of sialic acid-dependent cell adhesion molecules. In the present study, we show that CD33 is a fourth member of this family. As a model for sialic acid-dependent binding, human erythrocytes were derivatized with N-acetylneuraminic acid (NeuAc) in different linkages. A recombinant soluble form of CD33, Fc-CD33, bound red blood cells with a specificity similar to that of sialoadhesin, preferring NeuAc alpha 2,3Gal in N- and O-glycans over NeuAc alpha 2,6Gal in N-glycans. Fc-CD33 also bound selectively to the myeloid cell lines HL-60 and U937. However, CD33 was unable to mediate cell binding after transient expression in COS cells, despite high levels of surface expression. Pretreatment of the CD33-transfected cells with sialidase rendered them capable of mediating sialic acid-dependent binding. These results show that CD33 can function as a sialic acid-dependent cell adhesion molecule and that binding can be modulated by endogenous sialoglycoconjugates when CD33 is expressed in a plasma membrane.

Figures