Presence of platelet-derived growth factor in normal and fibrotic lung is specifically associated with interstitial macrophages, while both interstitial macrophages and alveolar epithelial cells express the c-sis proto-oncogene.
Presence of platelet-derived growth factor in normal and fibrotic lung is specifically associated with interstitial macrophages, while both interstitial macrophages and alveolar epithelial cells express the c-sis proto-oncogene.
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正常和纤维化肺中血小板衍生生长因子的存在与间质巨噬细胞特异性相关,而间质巨噬细胞和肺泡上皮细胞均表达 c-sis 原癌基因。
DOI:
10.1165/ajrcmb/5.6.531
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发表时间:
1991
影响因子:
6.4
通讯作者:
Yves Martinet
中科院分区:
文献类型:
--
作者:
J. Vignaud;Mustapha Allam;N. Martinet;Michael Pech;François Plénat;Yves Martinet
Normal lung structure is maintained by the presence of mesenchymal cells and their extracellular matrix products. The slow normal turnover of these cells is disrupted in fibrotic disorders, resulting in the in situ accumulation of mesenchymal cells and their extracellular matrix leading to a progressive alveolar wall thickening. Idiopathic pulmonary fibrosis (IPF) is a chronic fibrotic disorder of the lung characterized by a diffuse interstitial and intra-alveolar inflammation dominated by macrophages and polymorphonuclear neutrophils. Evaluation of alveolar macrophages (AM) obtained by bronchoalveolar lavage has previously shown that AM from normal individuals spontaneously release small amounts of platelet-derived growth factor (PDGF), a chemotactic and growth factor for mesenchymal cells, whereas AM from IPF patients spontaneously release increased amounts of biologically active PDGF, suggesting its involvement in mesenchymal cell accumulation. However, other cells such as endothelial cells and vascular smooth muscle cells can also release PDGF in vitro. In order to specify PDGF location in lung parenchyma, open lung biopsies from normal individuals and IPF patients were examined by immunohistochemistry using an anti-PDGF antibody and by in situ hybridization using PDGF A-chain and B-chain gene probes. In normal as well as in fibrotic lung, PDGF was only present in relation with interstitial macrophages but not with any other inflammatory cells or mesenchymal cells. Furthermore, the percentage of PDGF-positive macrophages in IPF was 3-fold increased in comparison to normal lung. In addition, the percentage of PDGF-positive macrophages was the same in fibrotic and nonfibrotic areas of IPF lungs.(ABSTRACT TRUNCATED AT 250 WORDS)
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DOI:
10.1146/annurev.cb.03.110187.002303
发表时间:
1987
期刊:
Annual review of cell biology
影响因子:
--
作者:
Deuel,TF
通讯作者:
Deuel,TF
DOI:
10.1172/jci113712
发表时间:
1988
期刊:
The Journal of clinical investigation
影响因子:
--
作者:
Sariban,E;Sitaras,NM;Antoniades,HN;Kufe,DW;Pantazis,P
通讯作者:
Pantazis,P
DOI:
10.1016/b978-0-12-152826-3.50012-7
发表时间:
1985
期刊:
Current topics in cellular regulation
影响因子:
--
作者:
Deuel,TF;Tong,BD;Huang,JS
通讯作者:
Huang,JS
影响因子:
2.7
作者:
COX, KH;DELEON, DV;ANGERER, RC
通讯作者:
ANGERER, RC
DOI:
10.1073/pnas.84.17.6020
发表时间:
1987-09-01
影响因子:
11.1
作者:
ASSOIAN, RK;FLEURDELYS, BE;SPORN, MB
通讯作者:
SPORN, MB