Neutrophil migration in opposing chemoattractant gradients using microfluidic chemotaxis devices

被引:79
作者
Lin, F
Nguyen, CMC
Wang, SJ
Saadi, W
Gross, SP
Jeon, NL [1 ]
机构
[1] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Phys & Astron, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92697 USA
关键词
chemotaxis; gradient; hierarchy; microfluidic; migration; neutrophil;
D O I
10.1007/s10439-005-2503-6
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Neutrophils migrating in tissue respond to complex overlapping signals generated by a variety of chemotactic factors (CFs). Previous studies suggested a hierarchy between bacteria-derived CFs and host-derived CFs but could not differentiate neutrophil response to potentially equal host-derived CFs (IL-8 and LTB4). This paper reports neutrophil migration in conflicting gradients of IL-8 and LTB4 using a microfluidic chemotaxis device that can generate stable and well-defined gradients. We quantitatively characterized the movement of cells from time-lapse images. Neutrophils migrate more efficiently toward single IL-8 gradients than single LTB4 gradients as measured by the effective chemotactic index (ECI). In opposing gradients of IL-8 and LTB4, neutrophils show obvious chemotaxis toward a distant gradient, consistent with previous reports. When an opposing gradient of LTB4 is present, neutrophils show less effective chemotaxis toward IL-8 than when they are in a gradient of IL-8 alone. In contrast, the chemotactic response of neutrophils to LTB4 is not reduced in opposing gradients as compared to that in a single LTB4 gradient. These results indicate that the presence of one host-derived CF modifies the response of neutrophils to a second CF suggesting a subtle hierarchy between them.
引用
收藏
页码:475 / 482
页数:8
相关论文
共 22 条
[11]   An intracellular signaling hierarchy determines direction of migration in opposing chemotactic gradients [J].
Heit, B ;
Tavener, S ;
Raharjo, E ;
Kubes, P .
JOURNAL OF CELL BIOLOGY, 2002, 159 (01) :91-102
[12]   Generation of solution and surface gradients using microfluidic systems [J].
Jeon, NL ;
Dertinger, SKW ;
Chiu, DT ;
Choi, IS ;
Stroock, AD ;
Whitesides, GM .
LANGMUIR, 2000, 16 (22) :8311-8316
[13]   A fibrin or collagen gel assay for tissue cell chemotaxis: Assessment of fibroblast chemotaxis to GRGDSP [J].
Knapp, DM ;
Helou, EF ;
Tranquillo, RT .
EXPERIMENTAL CELL RESEARCH, 1999, 247 (02) :543-553
[14]   Introduction: The complexities of leukocyte recruitment [J].
Kubes, P .
SEMINARS IN IMMUNOLOGY, 2002, 14 (02) :65-72
[15]   Effective neutrophil chemotaxis is strongly influenced by mean IL-8 concentration [J].
Lin, F ;
Nguyen, CMC ;
Wang, SJ ;
Saadi, W ;
Gross, SP ;
Jeon, NL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 319 (02) :576-581
[16]  
NELSON RD, 1975, J IMMUNOL, V115, P1650
[17]   Chemokines and chemokine receptors in leukocyte trafficking [J].
Olson, TS ;
Ley, K .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2002, 283 (01) :R7-R28
[18]   G protein signaling events are activated at the leading edge of chemotactic cells [J].
Parente, CA ;
Blacklock, BJ ;
Froehlich, WM ;
Murphy, DB ;
Devreotes, PN .
CELL, 1998, 95 (01) :81-91
[19]   Rho family proteins: coordinating cell responses [J].
Ridley, AJ .
TRENDS IN CELL BIOLOGY, 2001, 11 (12) :471-477
[20]   Sputum chemotactic activity in chronic obstructive pulmonary disease:: effect of α1-antitrypsin deficiency and the role of leukotriene B4 and interleukin 8 [J].
Woolhouse, IS ;
Bayley, DL ;
Stockley, RA .
THORAX, 2002, 57 (08) :709-714