ENHANCED EXPRESSION OF ALPHA(V) INTEGRIN SUBUNIT AND OSTEOPONTIN DURING DIFFERENTIATION OF HL-60 CELLS ALONG THE MONOCYTIC PATHWAY

被引:19
作者
SOMERMAN, MJ
BERRY, JE
KHALKHALIELLIS, Z
OSDOBY, P
SIMPSON, RU
机构
[1] UNIV MICHIGAN, DEPT PREVENT, ANN ARBOR, MI 48109 USA
[2] UNIV MICHIGAN, DEPT GERIATR, ANN ARBOR, MI 48109 USA
[3] UNIV MICHIGAN, DEPT PHARMACOL, ANN ARBOR, MI 48109 USA
[4] WASHINGTON UNIV, DEPT BIOL, ST LOUIS, MO 63130 USA
[5] WASHINGTON UNIV, DIV BONE & MINERAL DIS, ST LOUIS, MO 63130 USA
关键词
D O I
10.1006/excr.1995.1042
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
HL-60 cells, a promyelocytic leukemic cell line, provide a good model for studying the role of adhesion molecules and associated receptors involved in cell differentiation. When exposed to factors such as phorbol esters, these cells grown in suspension differentiate into monocytes and adhere to tissue culture dishes. In this study we showed that HL-60 cells exposed to phorbol esters express osteopontin (OPN), a cell adhesion molecule linked with osteoclast function. Moreover, the timed expression of OPN, in phorbol ester treated cells, was linked to increased cell adhesion. Subsequent to the expression of OPN, an increase in mRNA levels for alpha(V) integrin subunit was observed. The alpha(V) beta(3) integrin, a cell surface receptor found in high concentrations in osteoclasts, is considered to be a receptor for OPN. Furthermore, during differentiation we detected an increase in two cell surface markers specific for osteoclasts, 75B and 121F. This is the first report to demonstrate expression of OPN during differentiation of HL-60 cells, indicating that HL-60 cells can be used as a tool to enhance our understanding as to the role of OPN in cell differentiation. (C) 1995 Academic Press, Inc.
引用
收藏
页码:335 / 341
页数:7
相关论文
共 66 条
  • [51] INHIBITION OF CALCIUM-OXALATE CRYSTAL-GROWTH INVITRO BY UROPONTIN - ANOTHER MEMBER OF THE ASPARTIC ACID-RICH PROTEIN SUPERFAMILY
    SHIRAGA, H
    MIN, W
    VANDUSEN, WJ
    CLAYMAN, MD
    MINER, D
    TERRELL, CH
    SHERBOTIE, JR
    FOREMAN, JW
    PRZYSIECKI, C
    NEILSON, EG
    HOYER, JR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (01) : 426 - 430
  • [52] SINGH K, 1990, J BIOL CHEM, V265, P18696
  • [53] SLAVKIN H C, 1990, Critical Reviews in Oral Biology and Medicine, V1, P1
  • [54] SODEK J, 1992, INT CONGR SER, V1002, P297
  • [55] SOMERMAN MJ, 1987, J BONE MINER RES, V2, P259
  • [56] CELL ATTACHMENT ACTIVITY OF THE 44-KILODALTON BONE PHOSPHOPROTEIN IS NOT RESTRICTED TO BONE-CELLS
    SOMERMAN, MJ
    PRINCE, CW
    BUTLER, WT
    FOSTER, RA
    MOEHRING, JM
    SAUK, JJ
    [J]. MATRIX, 1989, 9 (01): : 49 - 54
  • [57] SUZUKI S, 1987, J BIOL CHEM, V262, P14080
  • [58] DISTRIBUTION OF EXPRESSION OF 2AR (OSTEOPONTIN) IN THE EMBRYONIC MOUSE INNER-EAR REVEALED BY INSITU HYBRIDIZATION
    SWANSON, GJ
    NOMURA, S
    HOGAN, BLM
    [J]. HEARING RESEARCH, 1989, 41 (2-3) : 169 - 177
  • [59] TANAKA H, 1982, BIOCHEM J, V204, P713, DOI 10.1042/bj2040713
  • [60] IDENTIFICATION OF OSTEOPONTIN IN ISOLATED RABBIT OSTEOCLASTS
    TEZUKA, K
    SATO, T
    KAMIOKA, H
    NIJWEIDE, PJ
    TANAKA, K
    MATSUO, T
    OHTA, M
    KURIHARA, N
    HAKEDA, Y
    KUMEGAWA, M
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 186 (02) : 911 - 917