Nitric oxide production by coelomocytes of Asterias forbesi

• Published in: Developmental and comparative immunology 2001, Vol.25 (1), p.1-10
• Main Authors: Beck, Gregory, Ellis, Thomas, Zhang, Haiyan, Lin, Wenyu, Beauregard, Karen, Habicht, Gail S., Truong, Nobel
• Format: Article
• Language: English
• Subjects: Animals; Arginine - analogs & derivatives; Asterias forbesi; Blotting, Western - veterinary; Coelomocyte; Culture Techniques - veterinary; Echinoderm; Evolution; Host defense; Immunity; Interleukin; Interleukin-1 - pharmacology; Invertebrate; Mice; Molecular Weight; Nitric Oxide - biosynthesis; Nitrites - metabolism; Phagocytes - drug effects; Phagocytes - metabolism; Rabbits; Starfish - metabolism
• ISSN: 0145-305X; 1879-0089
• DOI: 10.1016/S0145-305X(00)00036-7

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)-1α- and β-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-1-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 ≈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.