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Inhibition of granuloma‐associated angiogenesis by controlling mast cell mediator release: role of mast cell protease‐5
Author(s) -
Russo Annapina,
Russo Giulia,
Peticca Manuela,
Pietropaolo Concetta,
Di Rosa Massimo,
Iuvone Teresa
Publication year - 2005
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0706112
Subject(s) - angiogenesis , mast cell , chymase , proinflammatory cytokine , granuloma , chemistry , inflammation , biology , endocrinology , immunology , microbiology and biotechnology , medicine , cancer research
1 We investigated the role of mast cells in granuloma‐associated angiogenesis in rat by using: (i) a mast cell membrane stabilizer, ketotifen; (ii) a mast cell depleting agent, compound 48/80. Moreover, we focused on the role of chymases, which exhibit proinflammatory and proangiogenic properties by using: (i) chymostatin, an inhibitor of chymase activity; (ii) a specific antisense oligonucleotide (AS‐ODN) designed against rat mast cell protease‐5 (rMCP‐5), the most abundantly expressed chymase in the skin. 2 The formation of granuloma was evaluated, as wet weight, 96 h after the subcutaneous implant of two λ ‐carrageenin (1%)‐soaked sponges on the back of male Wistar rats. Angiogenesis was evaluated as haemoglobin content in the granulomatous tissue and as level of tumour necrosis factor‐ α (TNF‐ α ) in the exudates. 3 A single injection of ketotifen (1–5–25 mg kg −1 i.p.) significantly reduced granuloma formation by 31.6, 44.6 and 71.9%, and haemoglobin content by 17.0, 35.0 and 66.2%, suggesting that the release of mediator(s) from mast cells modulates the process. Chymostatin (5–10 nmol −1 site −1 day −1 ) reduced granuloma‐associated angiogenesis by 57.3 and 70.0%. 4 RT–PCR analysis showed that rMCP‐5 mRNA amounts were significantly reduced by rMCP‐5 AS‐ODN (1.25–2.5–5.0 nmol site −1 ) by 69.5, 72.5 and 81.8%. In parallel experiments, rMCP‐5 AS‐ODN (1.25, 2.5, 5.0 nmol site −1 ) strongly reduced granuloma weight (26.1, 45.0 and 56.3%) and haemoglobin content (22.2, 50.4, 62.03%), suggesting that the observed effect is mediated through an antisense mechanism. 5 In conclusion, these data suggest that: (i) inhibition of mast cell mediators release may represent a novel strategy to modulate angiogenesis; (ii) among the chymase family, rMCP‐5 is a key promoter of angiogenesis in the rat.British Journal of Pharmacology (2005) 145 , 24–33. doi: 10.1038/sj.bjp.0706112