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Matrix metalloproteinases regulate neutrophil‐endothelial cell adhesion through generation of endothelin‐1[1–32]
Author(s) -
FernandezPatron Carlos,
Zouki Christine,
Whittal Randy,
Chan John S. D.,
Davidge Sandra T.,
Filep János G.
Publication year - 2001
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.01-0178com
Subject(s) - chemistry , cd18 , gelatinase , microbiology and biotechnology , endothelial stem cell , endothelin 1 , cell adhesion , mapk/erk pathway , integrin alpha m , matrix metalloproteinase , kinase , receptor , biology , biochemistry , cell , in vitro
We recently reported that matrix metal‐loproteinase 2 (MMP‐2, gelatinase A) cleaves big endo‐thelin 1 (ET‐1), yielding the vasoactive peptide ET‐1[1–32]. We tested whether ET‐1[1–32] could affect the adhesion of human neutrophils to coronary artery endothelial cells (HCAEC). ET‐1[1–32] rapidly down‐regulated the expression of L‐selectin and up‐regulated expression of CD11b/CD18 on the neutrophil surface, with EC 50 values of 1–3 nM. These actions of ET‐1[1–32] were mediated via ET A receptors and did not require conversion of ET‐1[1–32] into ET‐1 by neutrophil proteases, as revealed by liquid chromatography and mass spectroscopy. Moreover, ET‐1[1–32] evoked release of neutrophil gelatinase B, which cleaved big ET‐1 to yield ET‐1[1–32], thus revealing a positive feedback loop for ET‐1[1–32] generation. Up‐regula‐tion of CD11b/CD18 expression and gelatinase release was tightly associated with activation of extracellular signal‐regulated kinase (Erk). Stimulation of Erk activity was due to activation of Ras, Raf‐1, and MEK (MAPK kinase). ET‐1[1–32] also produced slight increases in the expression of ICAM‐1 and E‐selectin on HCAEC, and markedly enhanced ß 2 integrin‐dependent adhesion of neutrophils to activated HCAEC. These results are the first indication that gelatinolytic MMPs via cleavage of big ET‐1 to yield ET‐1[1–32] activate neu‐trophils and promote leukocyte‐endothelial cell adhesion and, consequently, neutrophil trafficking into inflamed tissues.—Fernandez‐Patron, C., Zouki, C., Whittal, R., Chan, J. S. D., Davidge, S. T., Filep, J. G. Matrix metalloproteinases regulate neutrophil‐endothelial cell adhesion through generation of endothelin‐ 1[1–32]. FASEB J. 15, 2230–2240 (2001)