Fibronectin regulates the activation of THP-1 cells by TGF-β1

被引:19
作者
Wang, ACC [1 ]
Fu, L [1 ]
机构
[1] VA Healthcare Syst, Div Pulm & Crit Care, San Diego, CA 92161 USA
关键词
monocytes/macrophages; inflammation; adhesion molecules; inflammatory mediators; growth factors;
D O I
10.1007/s000110050738
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective and Design: To determine how fibronectin regulates the immunomodulatory effects of transforming growth factor (TGF)-beta on THP-1 cells. Material or Subjects: THP-1 monocytic cell line. Treatment: THP-I cells were primed for 48 h in the presence or absence of 250 pM TGF-beta1. Methods: Assays or assessments carried out, together with statistical test applied. Results: We found that adherence to fibronectin dramatically modulates the effects of TGF-beta1 on the human monocytic cell line THP-1. TGF-beta1 did not significantly affect constitutive interleukin (IL)-8 secretion or IL-1 beta -induced IL-8 secretion from suspended cells. In contrast, TGF-beta1 stimulated IL-8 secretion as well as augmented IL-1 beta -induced IL-8 secretion from adherent cells. The differential effects of TGF-beta1 on IL-8 secretion from suspended and adherent cells could not be explained by differences in IL-1 receptor antagonist production. The effects of fibronectin on TGF-beta1 induced IL-8 secretion from THP-1 cells were mimicked by adhesion to immobilized anti-alpha4 beta1 integrin antibody and to a fibronectin fragment containing the CS-1 domain. Conclusions: These results indicate that alpha4 beta1-mediated adhesion to fibronectin may play a key role during inflammation by profoundly influencing the effects of TGF-beta1 on monocytes.
引用
收藏
页码:142 / 148
页数:7
相关论文
共 31 条
[1]   RAPID ONSET SYNOVIAL INFLAMMATION AND HYPERPLASIA INDUCED BY TRANSFORMING GROWTH FACTOR-BETA [J].
ALLEN, JB ;
MANTHEY, CL ;
HAND, AR ;
OHURA, K ;
ELLINGSWORTH, L ;
WAHL, SM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (01) :231-247
[2]   TRANSFORMING GROWTH FACTOR-BETA INCREASES CELL-SURFACE BINDING AND ASSEMBLY OF EXOGENOUS (PLASMA) FIBRONECTIN BY NORMAL HUMAN-FIBROBLASTS [J].
ALLENHOFFMANN, BL ;
CRANKSHAW, CL ;
MOSHER, DF .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (10) :4234-4242
[3]   TGF-beta 1-stimulated adhesion of human mononuclear phagocytes to fibronectin and laminin is abolished by IFN-gamma: Dependence on alpha 5 beta 1 and beta 2 integrins [J].
Bauvois, B ;
VanWeyenbergh, J ;
Rouillard, D ;
Wietzerbin, J .
EXPERIMENTAL CELL RESEARCH, 1996, 222 (01) :209-217
[4]   TRANSFORMING GROWTH-FACTOR BETA-1 SUPPRESSES ACUTE AND CHRONIC ARTHRITIS IN EXPERIMENTAL-ANIMALS [J].
BRANDES, ME ;
ALLEN, JB ;
OGAWA, Y ;
WAHL, SM .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (03) :1108-1113
[5]  
CARLOS TM, 1994, BLOOD, V84, P2068
[6]  
CHANTRY D, 1989, J IMMUNOL, V142, P4295
[7]   Melanoma chondroitin sulphate proteoglycan regulates cell spreading through Cdc42, Ack-1 and p130cas [J].
Eisenmann, KM ;
McCarthy, JB ;
Simpson, MA ;
Keely, PJ ;
Guan, JL ;
Tachibana, K ;
Lim, L ;
Manser, E ;
Furcht, LT ;
Iida, J .
NATURE CELL BIOLOGY, 1999, 1 (08) :507-513
[8]   Blockade of CD49d (α4 integrin) on intrapulmonary but not circulating leukocytes inhibits airway inflammation and hyperresponsiveness in a mouse model of asthma [J].
Henderson, WR ;
Chi, EY ;
Albert, RK ;
Chu, SJ ;
Lamm, WJE ;
Rochon, Y ;
Jonas, M ;
Christie, PE ;
Harlan, JM .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (12) :3083-3092
[9]   Integrin α2β1 mediates isoform-specific activation of p38 and upregulation of collagen gene transcription by a mechanism involving the α2 cytoplasmic tail [J].
Ivaska, J ;
Reunanen, H ;
Westermarck, J ;
Koivisto, L ;
Kähäri, VM ;
Heino, J .
JOURNAL OF CELL BIOLOGY, 1999, 147 (02) :401-415
[10]   TRANSFORMING GROWTH FACTOR-BETA-1 NULL MUTATION IN MICE CAUSES EXCESSIVE INFLAMMATORY RESPONSE AND EARLY DEATH [J].
KULKARNI, AB ;
HUH, CG ;
BECKER, D ;
GEISER, A ;
LYGHT, M ;
FLANDERS, KC ;
ROBERTS, AB ;
SPORN, MB ;
WARD, JM ;
KARLSSON, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (02) :770-774