IDENTIFICATION OF CELL-SURFACE RECEPTORS FOR THE ACT-2 CYTOKINE

被引:23
作者
NAPOLITANO, M
SEAMON, KB
LEONARD, WJ
机构
[1] NICHHD, CELL BIOL & METAB BRANCH, BLDG 18T, ROOM 101, BETHESDA, MD 20892 USA
[2] US FDA, DIV BIOCHEM & BIOPHYS, BETHESDA, MD 20892 USA
关键词
D O I
10.1084/jem.172.1.285
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have identified cell surface receptors for Act-2, a secreted protein expressed upon activation of T cells, B cells, and monocytes. Although 125I-Act-2 showed little, if any, specific binding to resting peripheral blood lymphocytes (PBL) receptors were readily detected on PHA/PMAactivated PBL and a variety of cell lines including MT2, HL60, DMSO differentiated HL60, HeLa, and K562 cells. The equilibrium dissociation constant (Kd) is 3-12 nM for MT2, K562, and PBL activated with PHA/PMA for 40-80 h. We have also identified a rabbit polyclonal antiserum that can block Act-2 binding to its receptors. The ability to detect specific Act-2 receptors and the development of a blocking antiserum should prove valuable in efforts to molecularly clone the Act-2 receptor and to dissect the biological actions of Act-2. © 1990, Rockefeller University Press., All rights reserved.
引用
收藏
页码:285 / 289
页数:5
相关论文
共 13 条
[1]  
BROWN KD, 1989, J IMMUNOL, V142, P679
[2]   MYELOPOIETIC ENHANCING EFFECTS OF MURINE MACROPHAGE INFLAMMATORY PROTEIN-1 AND PROTEIN-2 ON COLONY FORMATION INVITRO BY MURINE AND HUMAN-BONE MARROW GRANULOCYTE MACROPHAGE PROGENITOR CELLS [J].
BROXMEYER, HE ;
SHERRY, B ;
LU, L ;
COOPER, S ;
CAROW, C ;
WOLPE, SD ;
CERAMI, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (05) :1583-1594
[3]   IDENTIFICATION OF A COMMON NUCLEOTIDE-SEQUENCE IN THE 3'-UNTRANSLATED REGION OF MESSENGER-RNA MOLECULES SPECIFYING INFLAMMATORY MEDIATORS [J].
CAPUT, D ;
BEUTLER, B ;
HARTOG, K ;
THAYER, R ;
BROWNSHIMER, S ;
CERAMI, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (06) :1670-1674
[4]   IDENTIFICATION AND CHARACTERIZATION OF AN INHIBITOR OF HEMATOPOIETIC STEM-CELL PROLIFERATION [J].
GRAHAM, GJ ;
WRIGHT, EG ;
HEWICK, R ;
WOLPE, SD ;
WILKIE, NM ;
DONALDSON, D ;
LORIMORE, S ;
PRAGNELL, IB .
NATURE, 1990, 344 (6265) :442-444
[5]  
LINDNER W, 1987, INT J PEPT PROT RES, V30, P794
[6]  
LIPESMA, 1988, P NATL ACAD SCI USA, V85, P9704
[7]  
MILLER MD, 1989, J IMMUNOL, V143, P2907
[8]   LIGAND - A VERSATILE COMPUTERIZED APPROACH FOR CHARACTERIZATION OF LIGAND-BINDING SYSTEMS [J].
MUNSON, PJ ;
RODBARD, D .
ANALYTICAL BIOCHEMISTRY, 1980, 107 (01) :220-239
[9]   A CDNA CLONE USED TO STUDY MESSENGER-RNA INDUCIBLE IN HUMAN TONSILLAR LYMPHOCYTES BY A TUMOR PROMOTER [J].
OBARU, K ;
FUKUDA, M ;
MAEDA, S ;
SHIMADA, K .
JOURNAL OF BIOCHEMISTRY, 1986, 99 (03) :885-894
[10]   A CONSERVED AU SEQUENCE FROM THE 3' UNTRANSLATED REGION OF GM-CSF MESSENGER-RNA MEDIATES SELECTIVE MESSENGER-RNA DEGRADATION [J].
SHAW, G ;
KAMEN, R .
CELL, 1986, 46 (05) :659-667