Membrane proteins of human fetal primitive nucleated red blood cells

Journal of Proteomics

Volumn 75, Issue 18, 2012, Pages 5762-5773

  Ponnusamy, Sukumar ^a   Zhang, Huoming ^a   Kadam, Priya ^a   Lin, Qingsong ^b   Lim, Teck Kwang ^b   Sandhu, Jaspal Singh ^a   Kothandaraman, Narasimhan ^a,d   Mahyuddin, Aniza Puteri ^a   Biswas, Arijit ^c   Venkat, Annapoorna ^c   Hew, Choy Leong ^b   Joshi, Shashikant B ^b   Chung, Maxey Ching Ming ^a,b   Choolani, Mahesh ^a  

^a NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

^b NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

^c NATIONAL UNIVERSITY HOSPITAL   (Singapore)

^d KING ABDULAZIZ UNIVERSITY   (Saudi Arabia)

Author keywords

2D LC MALDITOF TOF MS; Erythrocytes; Human fetal nucleated red blood cells; Membrane protein profiling; Noninvasive prenatal diagnosis; RBC

Indexed keywords

MEMBRANE ANTIGEN; MEMBRANE PROTEIN; PROTEOME;

ARTICLE; BIOINFORMATICS; CELL MEMBRANE; ERYTHROCYTE; FEMALE; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOCYTOCHEMISTRY; LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; MATERNAL BLOOD; PRENATAL DIAGNOSIS; PRIMITIVE FETAL NUCLEATED RED BLOOD CELL; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN LOCALIZATION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ERYTHROBLASTS; FEMALE; FETAL BLOOD; FETUS; HUMANS; MEMBRANE PROTEINS; PREGNANCY; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION;

EID: 84866164341     PISSN: 18743919     EISSN: 18767737     Source Type: Journal    
DOI: 10.1016/j.jprot.2012.07.020     Document Type: Article

References (46)

1. Palis J. Ontogeny of erythropoiesis. Curr Opin Hematol 2008, 15:155-161.
2. Choolani M., O'Donoghue K., Talbert D., Kumar S., Roberts I., Letsky E., et al. Characterization of first trimester fetal erythroblasts for non-invasive prenatal diagnosis. Mol Hum Reprod 2003, 9:227-235.
3. Van Handel B., Prashad S.L., Hassanzadeh-Kiabi N., Huang A., Magnusson M., Atanassova B., et al. The first trimester human placenta is a site for terminal maturation of primitive erythroid cells. Blood 2010, 116:3321-3330.
4. Peschle C., Mavilio F., Care A., Migliaccio G., Migliaccio A.R., Salvo G., et al. Haemoglobin switching in human embryos: asynchrony of zeta - alpha and epsilon - gamma-globin switches in primitive and definite erythropoietic lineage. Nature 1985, 313:235-238.
5. Qiu C., Olivier E.N., Velho M., Bouhassira E.E. Globin switches in yolk sac-like primitive and fetal-like definitive red blood cells produced from human embryonic stem cells. Blood 2008, 111:2400-2408.
6. Kakhniashvili D.G., Bulla L.A., Goodman S.R. The human erythrocyte proteome: analysis by ion trap mass spectrometry. Mol Cell Proteomics 2004, 3:501-509.
7. Low T.Y., Seow T.K., Chung M.C. Separation of human erythrocyte membrane associated proteins with one-dimensional and two-dimensional gel electrophoresis followed by identification with matrix-assisted laser desorption/ionization-time of flight mass spectrometry. Proteomics 2002, 2:1229-1239.
8. Bruschi M., Seppi C., Arena S., Musante L., Santucci L., Balduini C., et al. Proteomic analysis of erythrocyte membranes by soft Immobiline gels combined with differential protein extraction. J Proteome Res 2005, 4:1304-1309.
9. Tyan Y.C., Jong S.B., Liao J.D., Liao P.C., Yang M.H., Liu C.Y., et al. Proteomic profiling of erythrocyte proteins by proteolytic digestion chip and identification using two-dimensional electrospray ionization tandem mass spectrometry. J Proteome Res 2005, 4:748-757.
10. Pasini E.M., Kirkegaard M., Mortensen P., Lutz H.U., Thomas A.W., Mann M. In-depth analysis of the membrane and cytosolic proteome of red blood cells. Blood 2006, 108:791-801.
11. Zhang H., Lin Q., Ponnusamy S., Kothandaraman N., Lim T.K., Zhao C., et al. Differential recovery of membrane proteins after extraction by aqueous methanol and trifluoroethanol. Proteomics 2007, 7:1654-1663.
12. Roux-Dalvai F., Gonzalez de Peredo A., Simo C., Guerrier L., Bouyssie D., Zanella A., et al. Extensive analysis of the cytoplasmic proteome of human erythrocytes using the peptide ligand library technology and advanced mass spectrometry. Mol Cell Proteomics 2008, 7:2254-2269.
13. Pasini E.M., Kirkegaard M., Salerno D., Mortensen P., Mann M., Thomas A.W. Deep coverage mouse red blood cell proteome: a first comparison with the human red blood cell. Mol Cell Proteomics 2008, 7:1317-1330.
14. Eber S., Lux S.E. Hereditary spherocytosis-defects in proteins that connect the membrane skeleton to the lipid bilayer. Semin Hematol 2004, 41:118-141.
15. Kakhniashvili D.G., Griko N.B., Bulla L.A., Goodman S.R. The proteomics of sickle cell disease: profiling of erythrocyte membrane proteins by 2D-DIGE and tandem mass spectrometry. Exp Biol Med (Maywood) 2005, 230:787-792.
16. Lane P.A., Shew R.L., Iarocci T.A., Mohandas N., Hays T., Mentzer W.C. Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis. J Clin Invest 1987, 79:989-996.
17. Stewart G.W., Corrall R.J., Fyffe J.A., Stockdill G., Strong J.A. Familial pseudohyperkalaemia. A new syndrome. Lancet 1979, 2:175-177.
18. Delaunay J. The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations. Semin Hematol 2004, 41:165-172.
19. 2+-induced vesiculation in stomatin-deficient overhydrated hereditary stomatocytosis. Biochim Biophys Acta 2008, 1778:125-132.
20. Schrier S.L., Rachmilewitz E., Mohandas N. Cellular and membrane properties of alpha and beta thalassemic erythrocytes are different: implication for differences in clinical manifestations. Blood 1989, 74:2194-2202.
21. Roggwiller E., Betoulle M.E., Blisnick T., Braun Breton C. A role for erythrocyte band 3 degradation by the parasite gp76 serine protease in the formation of the parasitophorous vacuole during invasion of erythrocytes by Plasmodium falciparum. Mol Biochem Parasitol 1996, 82:13-24.
22. Cooper R.A., Carucci D.J. Proteomic approaches to studying drug targets and resistance in Plasmodium. Curr Drug Targets Infect Disord 2004, 4:41-51.
23. Pasini E.M., Lutz H.U., Mann M., Thomas A.W. Red blood cell (RBC) membrane proteomics-Part I: proteomics and RBC physiology. J Proteomics 2010, 73:403-420.
24. Pasini E.M., Lutz H.U., Mann M., Thomas A.W. Red blood cell (RBC) membrane proteomics-Part II: comparative proteomics and RBC patho-physiology. J Proteomics 2010, 73:421-435.
25. Mathew A., Bell A., Johnstone R.M. Hsp-70 is closely associated with the transferrin receptor in exosomes from maturing reticulocytes. Biochem J 1995, 308(Pt 3):823-830.
26. Voullaire L., Ioannou P., Nouri S., Williamson R. Fetal nucleated red blood cells from CVS washings: an aid to development of first trimester non-invasive prenatal diagnosis. Prenat Diagn 2001, 21:827-834.
27. Christensen B., Kolvraa S., Lykke-Hansen L., Lorch T., Gohel D., Smidt-Jensen S., et al. Studies on the isolation and identification of fetal nucleated red blood cells in the circulation of pregnant women before and after chorion villus sampling. Fetal Diagn Ther 2003, 18:376-384.
28. Nagy G.R., Ban Z., Sipos F., Beke A., Papp C., Papp Z. Isolation of epsilon-haemoglobin-chain positive fetal cells with micromanipulation for prenatal diagnosis. Prenat Diagn 2005, 25:398-402.
29. Choolani M., O'Donnell H., Campagnoli C., Kumar S., Roberts I., Bennett P.R., et al. Simultaneous fetal cell identification and diagnosis by epsilon-globin chain immunophenotyping and chromosomal fluorescence in situ hybridization. Blood 2001, 98:554-557.
30. Ponnusamy S., Mohammed N., Ho S.S., Zhang H.M., Chan Y.H., Ng Y.W., et al. In vivo model to determine fetal-cell enrichment efficiency of novel noninvasive prenatal diagnosis methods. Prenat Diagn 2008, 28:494-502.
31. Blonder J., Goshe M.B., Moore R.J., Pasa-Tolic L., Masselon C.D., Lipton M.S., et al. Enrichment of integral membrane proteins for proteomic analysis using liquid chromatography-tandem mass spectrometry. J Proteome Res 2002, 1:351-360.
32. Kersey P.J., Duarte J., Williams A., Karavidopoulou Y., Birney E., Apweiler R. The International Protein Index: an integrated database for proteomics experiments. Proteomics 2004, 4:1985-1988.
33. Lehr H.A., Mankoff D.A., Corwin D., Santeusanio G., Gown A.M. Application of photoshop-based image analysis to quantification of hormone receptor expression in breast cancer. J Histochem Cytochem 1997, 45:1559-1565.
34. Santoni V., Molloy M., Rabilloud T. Membrane proteins and proteomics: un amour impossible?. Electrophoresis 2000, 21:1054-1070.
35. Tan S., Tan H.T., Chung M.C. Membrane proteins and membrane proteomics. Proteomics 2008, 8:3924-3932.
36. Feingold E.A., Penny L.A., Nienhuis A.W., Forget B.G. An olfactory receptor gene is located in the extended human beta-globin gene cluster and is expressed in erythroid cells. Genomics 1999, 61:15-23.
37. Richardson B.M., Heesom K.J., Parsons S.F., Anstee D.J., Frayne J. Analysis of the differential proteome of human erythroblasts during in vitro erythropoiesis by 2-D DIGE. Proteomics Clin Appl 2009, 3:1123-1134.
38. Chhabra A., Lechner A.J., Ueno M., Acharya A., Van Handel B., Wang Y., et al. Trophoblasts regulate the placental hematopoietic niche through PDGF-B signaling. Dev Cell 2012, 22:651-659.
39. Leecharoenkiat A., Wannatung T., Lithanatudom P., Svasti S., Fucharoen S., Chokchaichamnankit D., et al. Increased oxidative metabolism is associated with erythroid precursor expansion in beta0-thalassaemia/Hb E disease. Blood Cells Mol Dis 2011, 47:143-157.
40. Sriiam S., Leecharoenkiat A., Lithanatudom P., Wannatung T., Svasti S., Fucharoen S., et al. Proteomic analysis of hemoglobin H-constant spring (Hb H-CS) erythroblasts. Blood Cells Mol Dis 2012, 48:77-85.
41. Pollack S., Campana T. Immature red cells have ferritin receptors. Biochem Biophys Res Commun 1981, 100:1667-1672.
42. Rider D.A., Young S.P. Measuring the specific activity of the CD45 protein tyrosine phosphatase. J Immunol Methods 2003, 277:127-134.
43. Hanspal M., Hanspal J.S. The association of erythroblasts with macrophages promotes erythroid proliferation and maturation: a 30-kD heparin-binding protein is involved in this contact. Blood 1994, 84:3494-3504.
44. Fabriek B.O., Polfliet M.M., Vloet R.P., van der Schors R.C., Ligtenberg A.J., Weaver L.K., et al. The macrophage CD163 surface glycoprotein is an erythroblast adhesion receptor. Blood 2007, 109:5223-5229.
45. Celis J.E., Celis P., Palsdottir H., Ostergaard M., Gromov P., Primdahl H., et al. Proteomic strategies to reveal tumor heterogeneity among urothelial papillomas. Mol Cell Proteomics 2002, 1:269-279.
46. Ohlsson G., Moreira J.M., Gromov P., Sauter G., Celis J.E. Loss of expression of the adipocyte-type fatty acid-binding protein (A-FABP) is associated with progression of human urothelial carcinomas. Mol Cell Proteomics 2005, 4:570-581.