TY - JOUR
T1 - Differential expression of CCR3 ligand mRNA in guinea pig lungs during allergen-induced inflammation
AU - Asano, K.
AU - Nakamura, M.
AU - Oguma, T.
AU - Fukunaga, K.
AU - Matsubara, H.
AU - Shiomi, T.
AU - Ishizaka, A.
AU - Yamaguchi, K.
AU - Kanazawa, M.
PY - 2001
Y1 - 2001
N2 - Objective and design: The gene expression profile of CCR3 ligands, eotaxin, RANTES, and monocyte chemo-attractant protein-3 (MCP-3), was examined in normal and inflamed guinea pig lungs. Material: Male Hartley guinea pigs (n = 49). Methods: Pulmonary mRNA was obtained from naive animals, animals treated with intravenous lipopolysaccharide administration, and animals repeatedly exposed to aerosolized allergen (ovalbumin). Northern analysis was performed to quantify pulmonary expression of eotaxin, RANTES, and MCP-3 mRNA. Pulmonary eosinophil peroxidase (EPO) activity was measured to quantify eosinophil accumulation. Results: Eotaxin and RANTES mRNAs, but not MCP-3 mRNA, were constitutively expressed in guinea pig lungs. Lipopolysaccharide treatment increased MCP-3 mRNA expression, but not eotaxin or RANTES mRNA. In contrast, allergen exposure in sensitized animals caused an increase in eotaxin mRNA, which demonstrated good temporal and quantitative correlation with pulmonary EPa activity, but not in MCP-3 or RANTES mRNA. Conclusions: Guinea pig CCR3 ligands demonstrated different gene expression profiles in normal and inflamed airways, suggesting that they play different physiological and pathophysiological roles in the airway.
AB - Objective and design: The gene expression profile of CCR3 ligands, eotaxin, RANTES, and monocyte chemo-attractant protein-3 (MCP-3), was examined in normal and inflamed guinea pig lungs. Material: Male Hartley guinea pigs (n = 49). Methods: Pulmonary mRNA was obtained from naive animals, animals treated with intravenous lipopolysaccharide administration, and animals repeatedly exposed to aerosolized allergen (ovalbumin). Northern analysis was performed to quantify pulmonary expression of eotaxin, RANTES, and MCP-3 mRNA. Pulmonary eosinophil peroxidase (EPO) activity was measured to quantify eosinophil accumulation. Results: Eotaxin and RANTES mRNAs, but not MCP-3 mRNA, were constitutively expressed in guinea pig lungs. Lipopolysaccharide treatment increased MCP-3 mRNA expression, but not eotaxin or RANTES mRNA. In contrast, allergen exposure in sensitized animals caused an increase in eotaxin mRNA, which demonstrated good temporal and quantitative correlation with pulmonary EPa activity, but not in MCP-3 or RANTES mRNA. Conclusions: Guinea pig CCR3 ligands demonstrated different gene expression profiles in normal and inflamed airways, suggesting that they play different physiological and pathophysiological roles in the airway.
KW - Asthma
KW - Eosinophil
KW - Eotaxin
KW - Monocyte chemoattractant protein
KW - RANTES
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UR - http://www.scopus.com/inward/citedby.url?scp=0035661228&partnerID=8YFLogxK
U2 - 10.1007/PL00000244
DO - 10.1007/PL00000244
M3 - Article
C2 - 11822789
AN - SCOPUS:0035661228
SN - 1023-3830
VL - 50
SP - 625
EP - 630
JO - Inflammation Research
JF - Inflammation Research
IS - 12
ER -