Inflammatory response in molluscs: Cross-taxa and evolutionary considerations

Current Pharmaceutical Design

Volumn 16, Issue 38, 2010, Pages 4160-4165

  Ottaviani, E ^a   Franchini, A ^a   Malagoli, D ^a  

^a UNIVERSITY OF MODENA AND REGGIO EMILIA   (Italy)

Author keywords

Evolution; Inflammation; Invertebrates

Indexed keywords

NITRIC OXIDE;

ARTICLE; HOMEOSTASIS; INFLAMMATION; INNATE IMMUNITY; INSECT; MOLECULAR EVOLUTION; MOLLUSC; NONHUMAN; PRIORITY JOURNAL; TISSUE INJURY; VERTEBRATE; WOUND HEALING;

ANIMALS; BIOLOGICAL EVOLUTION; HEMOCYTES; INFLAMMATION; MOLLUSCA; NITRIC OXIDE; WOUND HEALING;

EID: 79951716598     PISSN: 13816128     EISSN: None     Source Type: Journal    
DOI: 10.2174/138161210794519084     Document Type: Article

References (80)

1. Franchini A, Ottaviani E. Repair of molluscan tissue injury: role of PDGF and TGF-beta1. Tissue Cell 2000; 32: 312-21.
2. Ottaviani E. Insect immunorecognition. Inv Surv J 2005; 2: 142-51.
3. Ottaviani E. Molluscan immunorecognition. Inv Surv J 2006; 3: 50-63.
4. Dunn SR. Immunorecognition and immunoreceptors in the Cnidaria. Inv Surv J 2009; 6: 7-14.
5. Mitchinson MJ, Arno J, Edwards PAW, LePage RWF, Minson AC. Essentials of pathology. Oxford: Blackwell Science Ltd 1996.
6. Coleman WB, Tsongalis GJ. Molecular pathology. Amsterdam: Elsevier 2009.
7. Ottaviani E, Franceschi F. The invertebrate phagocytic immunocyte: clues to a common evolution of immune and neuroendocrine systems. Immunol Today 1997; 18: 169-74.
8. Ottaviani E, Franchini A, Franceschi C. Presence of immunoreactive molecules to CRH and cortisol in invertebrate haemocytes and lower and higher vertebrate thymus. Histochem J 1998; 30: 61-7.
9. Ottaviani E, Malagoli D, Franceschi C. Common evolutionary origin of the immune and neuroendocrine systems: from morphological and functional evidences to in silico approaches. Trends Immunol 2007; 28: 497-502.
10. Ottaviani E, Franchini A, Cossarizza A, Franceschi C. ACTH-like molecules in lymphocytes. A study in different vertebrate classes. Neuropeptides 1992; 23: 215-9.
11. Ottaviani E, Malagoli D, Capri M, Franceschi, C. Ecoimmunology: is there any room for the neuroendocrine system? BioEssays 2008; 30: 868-74.
12. Stadelmann WK, Digenis AG, Tobin GR. Physiology and healing dynamics of chronic cutaneous wounds. Am J Surg 1998; 176 (2A Suppl): 26S-38S.
13. Cheng TC, Galloway PC. Transplantation immunity in molluscs: the histoincompatibility of Helisoma duryi normale with allografts and xenografts. J Invert Pathol 1970; 15: 177-92.
14. Steenfos H, Lossing C, Hansson HA. Immunohistochemical demonstration of endogenous growth factors in wound healing. Wounds 1990; 2: 218-26.
15. Sminia T, Borghart-Reinders E, Van de Linde. Encapsulation of foreign materials experimentally introduced into the freshwater snail Lymnaea stagnalis. An electron microscopy and autoradiographic study. Cell Tissue Res 1974; 153: 307-26.
16. Ottaviani E, Vergine C. Allo-implant in the freshwater snail Planorbarius corneus (L.) (Gastropoda, Pulmonata). I. Histological and histochemical study. Zool Jb Physiol 1990; 94: 261-67.
17. Hughes TK, Smith EM, Chin R, et al. Interactions of immunoactive monokines (interleukin 1 and tumor necrosis factor) in the bivalve mollusc Mytilus edulis. Proc Natl Acad Sci USA 1990; 87: 4426-29.
18. Ottaviani E, Malagoli D, Franchini A. Invertebrate humoral factors: cytokines as mediators of cell survival. Prog Mol Subcell Biol 2004; 34: 1-25.
19. Koch AE, Polverini PJ, Kundel SL, et al. Interleukin-8 as a macrophage- derived mediator of angiogenesis. Science (Wash. DC) 1992; 258: 1798-1800.
20. Clark RAF. Fibronectin matrix deposition and fibronectin receptor expression in healing and normal skin. J Invest Derm 1990; 94: 128s-34s.
21. Blanton RA, Kupper TS, McDougall JK, Dower S. Regulation of interleukin 1 and its receptor in human keratinocytes. Proc Natl Acad Sci USA 1989; 86: 1273-77.
22. Sminia T, Pietersma K, Scheerboom JEM. Histological and ultrastructural observations on wound healing in the freshwater pulmonate Lymnaea stagnalis. Z Zellforsch 1973; 141: 561-73.
23. Ottaviani E, Franchini A, Vergine C. Allo-implant in the freshwater snail Planorbarius corneus (L.) (Gastropoda, Pulmonata). II. Immunocytochemical and ultrastructural study. Proc. 10th Malac Congr 1991; 289-94.
24. Ottaviani E, Franchini A, Kletsas D, Bernardi M, Genedani S. Involvement of PDGF and TGF-β in cell migration and phagocytosis in invertebrate and human immunocytes. Anim Biol 1997; 6: 91-5.
25. Roberts AB, Sporn MB, Assoian RK, et al. Transforming growth factor type beta: rapid induction of fibrosis and angiogenesis in vivo and stimulation of collagen formation in vitro. Proc Natl Acad Sci USA 1986; 83: 4167-71.
26. Mustoe TA, Pierce GF, Thomason A, Gramates P, Sporn MB, Deuel TF. Accelerated healing of incisional wounds in rats induced by transforming growth factor-β. Science 1987; 237: 1333-36.
27. Pierce GF, Mustoe TA, Lingelbach J, et al. Platelet-derived growth factor and transforming growth factor-β enhance tissue repair activities by unique mechanisms. J Cell Biol 1989; 109: 429-40.
28. Pierce GF, Vande Berg J, Rudolph R, Tarpley J, Mustoe TA. Platelet- derived growth factor-BB and transforming growth factor beta-1 selectively modulate glycosaminoglycans, collagen, and myofibroblasts in excisional wounds. Am J Pathol 1991; 138: 629-46.
29. Quaglino D, Nanney LB, Kennedy R, Davidson JM. Transforming growth factor-β stimulates wound healing and modulates extracellular matrix gene expression in pig skin. I. Excisional wound model. Lab Invest 1990; 63: 307-19.
30. Quaglino D, Nanney LB, Ditesheim JA, Davidson JM. Transforming growth factor-beta stimulates wound healing and modulates extracellular matrix gene expression in pig skin. Incisional wound model. J Invest Dermatol 1991; 97: 34-42.
31. Schmid P, Kunz S, Cerletti N, McMaster G, Cox D. Injury induced expression of TGF-β1 mRNA is enhanced by exogenously applied TGF-βs. Biochem Biophys Res Commun 1993; 194: 399-406.
32. Grotendorst GR, Martin GR, Pencev D, Sodek J, Harvey AK. Stimulation of granulation tissue formation by platelet-derived growth factor in normal and diabetic rats. J Clin Invest 1985; 76: 2323-29.
33. Pierce GF, Mustoe TA, Altrock BW, Duel TF, Thomason A. Role of platelet-derived growth factor in wound healing. J Cell Biochem 1991; 45: 319-26.
34. Pierce GF, Tarpley JE, Yanagihara D, Mustoe TA, Fox GM, Thomason A. Platelet-derived growth factor (BB homodimer), and transforming growth factor-beta 1, and basic fibroblast growth factor in dermal wound healing. Neovessel and matrix formation and cessation of repair. Am J Pathol 1992; 140: 1375-88.
35. Cromack DT, Porras-Reyes B, Mustoe TA. Current concepts in wound healing: growth factor and macrophage interaction. J Trauma 1990; 30 (suppl.): S129-S133.
36. Lelong C, Mathieu M, Favrel P. Structure and expression of mGDF, a new member of the transforming growth factor-β superfamily in the bivalve mollusc Crassostrea gigas. Eur J Biochem 2000; 267: 3986-93.
37. Lelong C, Badariotti F, Le Quéré H, Rodet F, Dubos MP, Favrel P. Cg-TGF-beta, a TGF-beta/activin homologue in the Pacific Oyster Crassostrea gigas, is involved in immunity against Gram-negative microbial infection. Dev Comp Immunol 2007; 31: 30-8.
38. Franchini A, Malagoli D, Ottaviani E. Cytokines and invertebrates: TGF-beta and PDGF. Curr Pharm Des 2006; 12: 3025-31.
39. Hudlicka O. Development of microcirculation: capillary growth and adaption. In: Renkin EM, Michel CC, Eds. Handbook of physiology, section 2: The cardiovascular system, vol. IV Microcirculation, part 1. Baltimore: Waverly Press 1984; pp. 165-216.
40. Majno G. Chronic inflammation: links with angiogenesis and wound healing. Am J Pathol 1998; 153: 1035-9.
41. Schmeisser A, Garlichs CD, Zhang H, et al. Monocytes coexpress endothelial and macrophagocytic lineage markers and form cordlike structures in Matrigel under angiogenic conditions. Cardiovasc Res 2001; 49: 671-680.
42. Rehman J, Li J, Orschell CM, March KL. Peripheral blood "endothelial progenitor cells" are derived from monocyte/macrophages and secrete angiogenic growth factors. Circulation 2003; 107: 1164-69.
43. Grenier G, Scimè A, Le Grand F, et al. Resident endothelial precursors in muscle, adipose, and dermis contribute to postnatal vasculogenesis. Stem Cells 2007; 25:3101-10.
44. de Eguileor M, Tettamanti G, Grimaldi A, et al. Histopathological changes after induced injury in leeches. J Invertebr Pathol 1999; 74: 14-28.
45. Grossi CE, Cadoni A, Zicca A, Leprini A, Ferrarini M. Large granular lymphocytes in human peripheral blood: ultrastructural and cytochemical characterization of the granules. Blood 1982; 59: 277-83.
46. Mikkelsen HB, Rumessen JJ. Characterization of macrophage-like cells in the external layers of human small and large intestine. Cell Tissue Res 1992; 270: 273-79.
47. Rowly AF, Ratcliffe NA. A histological study of wound healing and hemocyte function in the wax-moth Galleria mellonella. J Morph 1978; 157: 181-200.
48. Jacinto A, Martinez-Arias A, Martin P. Mechanisms of epithelial fusion and repair. Nat Cell Biol 2001; 3: E117-23.
49. Rämet M, Lanot R, Zachary D, Manfruelli P. JNK signaling pathway is required for efficient wound healing in Drosophila. Dev Biol 2002; 241: 145-156.
50. Wood W, Jacinto A, Grose R, et al. Wound healing recapitulates morphogenesis in Drosophila embryos. Nat Cell Biol 2002; 4: 907-12.
51. Stramer B, Wood W, Galko MJ, et al. Live imaging of wound inflammation in Drosophila embryos reveals key roles for small GTPases during in vivo cell migration. J Cell Biol 2005; 168: 567-73.
52. Wood W, Faria C, Jacinto A. Distinct mechanisms regulate hemocyte chemotaxis during development and wound healing in Drosophila melanogaster. J Cell Biol 2006; 173:405-16.
53. Wood W, Jacinto A. Drosophila melanogaster embryonic haemocytes: masters of multitasking. Nat Rev Mol Cell Biol 2007; 8:542-51.
54. Nakatogawa S, Oda Y, Kamiya M, et al. A novel peptide mediates aggregation and migration of hemocytes from an insect. Curr Biol 2009; 19:779-85.
55. Pae HO, Lee YC, Jo EK, Chung HT. Subtle interplay of endogenous bioactive gases (NO, CO and H(2)S) in inflammation. Arch Pharm Res 2009; 32: 1155-62.
56. Franchini A, Conte A, Ottaviani E. Nitric oxide: an ancestral immunocyte effector molecule. Adv Neuroimmunol 1995; 5: 463-78.
57. Radomski MW, Martin JF, Moncada S. Synthesis of nitric oxide by the haemocytes of the american horseshoe crab (Limulus polyphemus). Phil Trans R Soc Lond B 1991; 334: 129-133.
58. Ottaviani E, Paeman LR, Cadet P, Stefano GB. Evidence for nitric oxide production and utilization as a bacteriocidal agent by invertebrate immunocytes. Eur J Pharmacol 1993; 248: 319-24.
59. Ottaviani E, Barbieri D, Malagoli D, Franchini A. Nitric oxide induces apoptosis in the fat body cell line IPLB-LdFB from the insect Lymantria dispar. Comp Biochem Physiol 2001; 128B: 247-54.
60. Conte A, Ottaviani E. Nitric oxide synthase activity in molluscan hemocytes. FEBS Lett 1995; 365: 120-24.
61. Stefano GB, Ottaviani E. The biochemical substrate of nitric oxide signaling is present in primitive non-cognitive organisms. Brain Res 2002; 924: 82-9.
62. Novas A, Cao A, Barcia R, Ramos-Martinez JI. Nitric oxide release by hemocytes of the mussel Mytilus galloprovincialis Lmk was provoked by interleukin-2 but not by lipopolysaccharide. Int J Biochem Cell Biol 2004; 36: 390-94.
63. Novas A, Barcia R, Ramos-Martínez JI. Nitric oxide production by haemocytes from Mytilus galloprovincialis shows seasonal variations. Fish Shellfish Immunol 2007; 23: 886-91.
64. de Barros CM, de Carvalho DR, Andrade LR, Pavão MS, Allodi S. Nitric oxide production by hemocytes of the ascidian Styela plicata. Cell Tissue Res 2009; 338: 117-28.
65. Zhang T, Kawakami K, Qureshi MH, Okamura H, Kurimoto M, Saito A. Interleukin-12 (IL-12) and IL-18 synergistically induce the fungicidal activity of murine peritoneal exudate cells against Cryptococcus neoformans through production of gamma interferon by natural killer cells. Infect Immun 1997; 65: 3594-99.
66. Ottaviani E, Franchini A, Cassanelli S, Genedani S. Cytokines and invertebrate immune responses. Biol Cell 1995; 85: 87-91.
67. Sharma JN, Al-Omran A, Parvathy SS. Role of nitric oxide in inflammatory diseases. Inflammopharmacology 2007; 15: 252-59.
68. Moilanen E, Vapaatalo H. Nitric oxide in inflammation and immune response. Ann Med 1995; 27: 359-67.
69. Childress BB, Stechmiller JK. Role of nitric oxide in wound healing. Biol Res Nurs 2002; 4: 5-15.
70. Canesi L, Ciacci C, Betti M, et al. Immunotoxicity of carbon black nanoparticles to blue mussel hemocytes. Environ Int 2008; 34: 1114-9.
71. Chao CC, Park SH, Aust A. Participation of nitric-oxide and iron in the oxidation of DNA in asbestos-treated human lung epithelialcells. Arch Biochem Biophys 1996; 326: 152-57.
72. Brown DM, Roberts NK, Donaldson K. Effect of coating with lung lining fluid on the ability of fibres to produce a respiratory burst in rat alveolar macrophages. Toxicol In Vitro 1998; 12: 15-24.
73. Chin BY, Choi ME, Burdick MD, Strieter RM, Risby TH, Choi AM. Induction of apoptosis by particulate matter: role of TNFalpha and MAPK. Am J Physiol 1998; 275: L942-9.
74. Bonvallot V, Baeza-Squiban A, Boland S, Marano F. Activation of transcription factors by diesel exhaust particles in human bronchial epithelial cells in vitro. Inhal Toxicol 2000; 12: 359-64.
75. Aamm BB, Fonnum F. Carbon black particles increase reactive oxygen species formation in rat alveolar macrophages in vitro. Arch Toxicol 2007; 230: 207-18.
76. Konishi I, Hosokawa M, Sashima T, Maoka T, Miyashita K. Suppressive effects of alloxanthin and diatoxanthin from Halocynthia roretzi on LPS-induced expression of pro-inflammatory genes in RAW264.7 cells. J Oleo Sci 2008; 57: 181-9.
77. Moilanen E, Moilanen T, Knowles R, et al. Nitric oxide synthase is expressed in human macrophages during foreign body inflammation. Am J Pathol 1997; 150: 881-7.
78. Xu CX, Jin H, Chung YS, et al. Chondroitin sulfate extracted from the Styela clava tunic suppresses TNF-alpha-induced expression of inflammatory factors, VCAM-1 and iNOS by blocking Akt/NFkappaB signal in JB6 cells. Cancer Lett 2008; 264: 93-100.
79. Kim W, Moon SO, Lee S, Sung MJ, Kim SH, Park SK. Adrenomedullin reduces VEGF-induced endothelial adhesion molecules and adhesiveness through a phosphatidylinositol 3'-kinase pathway. Arterioscler Thromb Vasc Biol 2003; 23: 1377-83.
80. Kim HG, Shrestha B, Lim SY, et al. Cordycepin inhibits lipopolysaccharide- induced inflammation by the suppression of NF-kappaB through Akt and p38 inhibition in RAW 264.7 macrophage cells. Eur J Pharmacol 2006; 545: 192-9.