Nitric oxide production by coelomocytes of Asterias forbesi

被引:48
作者
Beck, G
Ellis, T
Zhang, HY
Lin, WY
Beauregard, K
Habicht, GS
Truong, N
机构
[1] Univ Massachusetts, Dept Biol, Boston, MA 02125 USA
[2] SUNY Stony Brook, Dept Pathol, Stony Brook, NY 11794 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
invertebrate; evolution; interleukin; coelomocyte; echinoderm; immunity; host defense;
D O I
10.1016/S0145-305X(00)00036-7
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Vertebrate mononuclear phagocytes produce a plethora of molecules involved in host defense. Among the most potent are the reactive oxygen and nitrogen intermediates. Coelomocytes from invertebrates subserve many of the same functions. In order to determine whether invertebrate phagocytes employ reactive nitrogen intermediates, we investigated the effect of various nonspecific stimulators and invertebrate interleukin (IL)-1 alpha- and beta-like molecules on nitric oxide (NO) production. Elevated NO release by stimulated coelomocytes was seen after 24 h. Incubation of stimulated coelomocytes in the presence of arginine analogs inhibited NO release. When invertebrate IL-l-like molecules were added to the coelomocytes, they stimulated the release of NO. Western blot analysis using a polyclonal rabbit antiserum to murine NO synthase detected a band at approximate to 125 kDa. These data indicate that coelomocytes are capable of producing and releasing NO and that NO is a chemical mediator that has been conserved as a host defense weapon of phagocytes through evolutionary time. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 57 条
[41]   NITRIC-OXIDE AS A SECRETORY PRODUCT OF MAMMALIAN-CELLS [J].
NATHAN, C .
FASEB JOURNAL, 1992, 6 (12) :3051-3064
[42]   SECRETORY PRODUCTS OF MACROPHAGES [J].
NATHAN, CF .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (02) :319-326
[43]  
Nighorn A, 1998, J NEUROSCI, V18, P7244
[44]   INFLAMMATION, IMMUNOREGULATION, AND INDUCIBLE NITRIC-OXIDE SYNTHASE [J].
NUSSLER, AK ;
BILLIAR, TR .
JOURNAL OF LEUKOCYTE BIOLOGY, 1993, 54 (02) :171-178
[45]   THERE IS MORE THAN ONE INTERLEUKIN-1 [J].
OPPENHEIM, JJ ;
KOVACS, EJ ;
MATSUSHIMA, K ;
DURUM, SK .
IMMUNOLOGY TODAY, 1986, 7 (02) :45-56
[46]   EVIDENCE FOR NITRIC-OXIDE PRODUCTION AND UTILIZATION AS A BACTERIOCIDAL AGENT BY INVERTEBRATE IMMUNOCYTES [J].
OTTAVIANI, E ;
PAEMEN, LR ;
CADET, P ;
STEFANO, GB .
EUROPEAN JOURNAL OF PHARMACOLOGY-ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY SECTION, 1993, 248 (04) :319-324
[47]  
OTTSVIANI E, 1995, BIOL CELL, V85, P87
[48]   NITRIC-OXIDE SYNTHESIS BY RAT PLEURAL MESOTHELIAL CELLS - INDUCTION BY CYTOKINES AND LIPOPOLYSACCHARIDE [J].
OWENS, MW ;
GRISHAM, MB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (02) :L110-L116
[49]   Localization of interleukin-1 beta mRNA in the cerebral ganglion of the protochordate, Styela plicata [J].
Pestarino, M ;
DeAnna, E ;
Masini, MA ;
Sturla, M .
NEUROSCIENCE LETTERS, 1997, 222 (03) :151-154
[50]   INVERTEBRATE CYTOKINES - TUNICATE CELL-PROLIFERATION STIMULATED BY AN INTERLEUKIN-1-LIKE MOLECULE [J].
RAFTOS, DA ;
COOPER, EL ;
HABICHT, GS ;
BECK, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (21) :9518-9522