A human cell-surface glycoprotein that carries Cromer-related blood group antigens on erythrocytes and is also expressed on leucocytes and platelets
- PMID: 3679286
- PMCID: PMC1453983
A human cell-surface glycoprotein that carries Cromer-related blood group antigens on erythrocytes and is also expressed on leucocytes and platelets
Abstract
A new human erythrocyte glycoprotein has been identified by immunoblotting with murine monoclonal antibodies under non-reducing conditions. The glycoprotein has a MW of 70,000 and carries Cromer-related blood group antigens. The monoclonal antibodies also react with normal peripheral blood leucocytes and platelets and several haemopoietic cell lines. The glycoprotein has a reduced MW after sialidase treatment. The MW is markedly reduced in Tn erythrocyte membranes and slightly increased in Cad erythrocyte membranes. These results suggest that the glycoprotein has a substantial content of O-glycans. The glycoprotein appears to be absent from, or grossly altered in, the erythrocytes of two individuals with the rare Inab phenotype.
Similar articles
-
The Ina and Inb blood group antigens are located on a glycoprotein of 80,000 MW (the CDw44 glycoprotein) whose expression is influenced by the In(Lu) gene.Immunology. 1988 May;64(1):37-43. Immunology. 1988. PMID: 2454887 Free PMC article.
-
Studies on the distribution of the antigens detected by some newly prepared monoclonal antibodies in normal hemopoietic and leukemic cells.Neoplasma. 1985;32(6):657-62. Neoplasma. 1985. PMID: 4088385
-
Erythrocyte antigens on human platelets.Prog Clin Biol Res. 1983;133:53-7. Prog Clin Biol Res. 1983. PMID: 6622497 No abstract available.
-
Blood group MNSs-active sialoglycoproteins of the human erythrocyte membrane.Prog Clin Biol Res. 1980;43:67-98. Prog Clin Biol Res. 1980. PMID: 6999510 Review.
-
[The use of surface antigens of erythroid cells in the study of hemoblastoses].Eksp Onkol. 1987;9(3):9-16. Eksp Onkol. 1987. PMID: 3301313 Review. Russian.
Cited by
-
Presence of the Dr receptor in normal human tissues and its possible role in the pathogenesis of ascending urinary tract infection.Am J Pathol. 1988 Oct;133(1):1-4. Am J Pathol. 1988. PMID: 3052090 Free PMC article.
-
Studies on the defect which causes absence of decay accelerating factor (DAF) from the peripheral blood cells of an individual with the Inab phenotype.Biochem J. 1989 Jul 15;261(2):489-93. doi: 10.1042/bj2610489. Biochem J. 1989. PMID: 2476116 Free PMC article.
-
CD55 is over-expressed in the tumour environment.Br J Cancer. 2001 Jan 5;84(1):80-6. doi: 10.1054/bjoc.2000.1570. Br J Cancer. 2001. PMID: 11139317 Free PMC article.
-
Complement regulatory proteins in early human fetal life: CD59, membrane co-factor protein (MCP) and decay-accelerating factor (DAF) are differentially expressed in the developing liver.Immunology. 1993 Oct;80(2):183-90. Immunology. 1993. PMID: 7505254 Free PMC article.
-
New monoclonal antibodies in CD59: use for the analysis of peripheral blood cells from paroxysmal nocturnal haemoglobinuria (PNH) patients and for the quantitation of CD59 on normal and decay accelerating factor (DAF)-deficient erythrocytes.Immunology. 1992 Mar;75(3):507-12. Immunology. 1992. PMID: 1374058 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous