Dermal fibroblasts represent a potent major source of human eotaxin: In vitro production and cytokine-mediated regulation

被引:40
作者
Miyamasu, M
Nakajima, T
Misaki, Y
Izumi, S
Tsuno, N
Kasahara, T
Yamamoto, K
Morita, Y
Hirai, K
机构
[1] Univ Tokyo, Sch Med, Dept Bioregulatory Funct, Bunkyo Ku, Tokyo 113, Japan
[2] Univ Tokyo, Sch Med, Dept Med & Phys Therapy, Bunkyo Ku, Tokyo 113, Japan
[3] Kyushu Univ, Med Inst Bioregulat, Dept Clin Immunol, Ohita, Japan
[4] Univ Tokyo, Sch Med, Dept Transfus & Med, Tokyo, Japan
[5] Kyoritsu Coll Pharm, Dept Biochem, Tokyo, Japan
关键词
ELISA; eotaxin; fibroblast; IL-4; TNF-alpha;
D O I
10.1006/cyto.1999.0487
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Accumulating evidence indicates that eotaxin plays an integral role in tissue recruitment of eosinophils in humans as well as in animals, To clarify which types of cells are actually important as sources of human eotaxin, we used a specific enzyme-linked immunosorbent assay (ELISA) to compare various types of hemopoietic and nonhemopoietic cells for the ability to produce eotaxin protein. Regardless of various conditioning, we failed to determine any significant eotaxin generation by peripheral leukocytes and vein endothelial cells (less than 20 pg/ml), A small amount of immunoreactive eotaxin was detected in cultures of A549 bronchial epithelial cell line cells. In contrast, dermal fibroblasts were capable of generating extremely high, and potentially biologically relevant, amounts of eotaxin protein (an the order of ng/ml), The eotaxin generation was induced by tumour necrosis factor alpha (TNF-alpha) or IL-4, and the production was drastically increased by combined use of these cytokines, Because fibroblasts are ideally situated within the interstium at the sites of allergic responses, our finding that these cells represent an important cellular source of eotaxin suggests that fibroblast-derived eotaxin may act to regulate eosinophil recruitment in a paracrine fashion. (C) 1999 Academic Press.
引用
收藏
页码:751 / 758
页数:8
相关论文
共 36 条
[21]  
MOSER R, 1993, J LAB CLIN MED, V122, P567
[22]   Intracellular localization and release of eotaxin from normal eosinophils [J].
Nakajima, T ;
Yamada, H ;
Iikura, M ;
Miyamasu, M ;
Izumi, S ;
Shida, H ;
Ohta, K ;
Imai, T ;
Yoshie, O ;
Mochizuki, M ;
Schröder, JM ;
Morita, Y ;
Yamamoto, K ;
Hirai, K .
FEBS LETTERS, 1998, 434 (03) :226-230
[23]   Cloning of the human eosinophil chemoattractant, eotaxin - Expression, receptor binding, and functional properties suggest a mechanism for the selective recruitment of eosinophils [J].
Ponath, PD ;
Qin, SX ;
Ringler, DJ ;
ClarkLewis, I ;
Wang, J ;
Kassam, N ;
Smith, H ;
Shi, XJ ;
Gonzalo, JA ;
Newman, W ;
GutierrezRamos, JC ;
Mackay, CR .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (03) :604-612
[24]   Molecular cloning and characterization of a human eotaxin receptor expressed selectively on eosinophils [J].
Ponath, PD ;
Qin, SX ;
Post, TW ;
Wang, J ;
Wu, L ;
Gerard, NP ;
Newman, W ;
Gerard, C ;
Mackay, CR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (06) :2437-2448
[25]  
RATHANASWAMI P, 1993, J BIOL CHEM, V268, P5834
[26]   MURINE EOTAXIN - AN EOSINOPHIL CHEMOATTRACTANT INDUCIBLE IN ENDOTHELIAL-CELLS AND IN INTERLEUKIN 4-INDUCED TUMOR SUPPRESSION [J].
ROTHENBERG, ME ;
LUSTER, AD ;
LEDER, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (19) :8960-8964
[27]   Selective expression of the eotaxin receptor CCR3 by human T helper 2 cells [J].
Sallusto, F ;
Mackay, CR ;
Lanzavecchia, A .
SCIENCE, 1997, 277 (5334) :2005-2007
[28]  
SCHLEIMER RP, 1992, J IMMUNOL, V148, P1086
[29]  
Smith RS, 1997, AM J PATHOL, V151, P317
[30]  
STANDIFORD TJ, 1990, J IMMUNOL, V145, P1435