Expression of matrix metalloproteinases and tissue inhibitors of metalloproteinases during normal human pulmonary development

被引:36
作者
Masumoto, K
de Rooij, JD
Suita, S
Rottier, R
Tibboel, D
de Krijger, RR
机构
[1] Erasmus MC Univ Med Ctr, Josephine Nefkens Inst, Dept Pathol, NL-3000 DR Rotterdam, Netherlands
[2] Erasmus MC Sophia, Dept Paediat Surg, Rotterdam, Netherlands
[3] Kyushu Univ, Grad Sch Med Sci, Dept Paediat Surg Reprod & Dev Med, Fukuoka 812, Japan
关键词
development; human fetal lung; MMP; TIMP;
D O I
10.1111/j.1365-2559.2005.02228.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Aims: Matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) are thought to be involved in lung development because they play an important role in the turnover of the extracellular matrix. Although limited data on MMP and TIMP expression are available from animal studies during prenatal pulmonary development, little is known about their expression during human fetal lung development. The aim of this study was to investigate the expression of MMP-1, -2, -9, TIMP-1, -2 and -3 in human fetal lungs from 9 to 42 weeks of gestation. Methods and results: Forty-five normal human fetal lung samples were analysed by immunohistochemistry. MMP-1, -9, TIMP-1, -2 and -3, but not MMP-2, were expressed in the epithelium at all gestational ages. The endothelium of all vessels and the arterial smooth muscle cells expressed MMP-1, -2, -9, TIMP-2 and -3, but not TIMP-1, at all developmental stages. Conclusion: The extensive distribution of MMPs and TIMPs throughout all stages of human lung development suggests that they play a significant role in the remodelling that occurs in the interstitium and epithelial basement membrane during lung development and in pulmonary vascular development. These data will serve as a base line for comparison with neonatal lung pathology, including pulmonary hypertension.
引用
收藏
页码:410 / 419
页数:10
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