INCREASED EXPRESSION OF GROWTH-FACTOR GENES FOR MACROPHAGES AND FIBROBLASTS IN BRONCHOALVEOLAR LAVAGE CELLS OF A PATIENT WITH PULMONARY HISTIOCYTOSIS-X

被引:9
作者
BARTH, J [1 ]
KREIPE, H [1 ]
RADZUN, HJ [1 ]
HEIDORN, K [1 ]
PETERMANN, W [1 ]
BEWIG, B [1 ]
PARWARESCH, MR [1 ]
机构
[1] UNIV KIEL,DEPT PATHOL,W-2300 KIEL 1,GERMANY
关键词
D O I
10.1136/thx.46.11.835
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Pulmonary histiocytosis X is the local manifestation of a systemic disorder of unknown cause characterised by infiltration of Langerhans cell like histiocytes and parenchymal fibrosis. In a male smoker with histologically proved histiocytosis X and functional impairment bronchoalveolar lavage showed an increase in CD-1/OKT-6 antigen positive histiocytes to 8%. Northern blot analysis of RNA from bronchoalveolar lavage cells showed an exaggerated expression of the M-CSF gene and of the c-fms gene encoding for the corresponding receptor. An increased level of c-sis RNA, which encodes the B chain of platelet derived growth factor, was also found. Diffuse reticulonodular infiltrates on the chest radiograph resolved with glucocorticoid treatment and CD-1/OKT-6 antigen positive histiocytes fell to 3%. Macrophage colony stimulating factor, c-fms and c-sis gene expression were reduced almost to normal after treatment. The results suggest that macrophage colony stimulating factor and platelet derived growth factor may have a role in the initiation or maintenance of pathological reactions in pulmonary histiocytosis X.
引用
收藏
页码:835 / 838
页数:4
相关论文
共 18 条
[1]   DIMINISHED ACTIVITY OF TARTRATE RESISTANT ACID-PHOSPHATASE IN ALVEOLAR MACROPHAGES FROM PATIENTS WITH ACTIVE SARCOIDOSIS [J].
BARTH, J ;
KREIPE, H ;
KIEMLEKALLEE, J ;
RADZUN, HJ ;
PARWARESCH, MR ;
PETERMANN, W .
THORAX, 1988, 43 (11) :901-904
[2]  
CHIU IM, 1984, CELL, V37, P123
[3]  
CLEVELAND DW, 1980, CELL, V20, P90
[4]   PLATELET-DERIVED GROWTH-FACTOR - STRUCTURE, FUNCTION, AND ROLES IN NORMAL AND TRANSFORMED-CELLS [J].
DEUEL, TF ;
HUANG, JS .
JOURNAL OF CLINICAL INVESTIGATION, 1984, 74 (03) :669-676
[5]   MCDONOUGH FELINE SARCOMA-VIRUS - CHARACTERIZATION OF THE MOLECULARLY CLONED PROVIRUS AND ITS FELINE ONCOGENE (V-FMS) [J].
DONNER, L ;
FEDELE, LA ;
GARON, CF ;
ANDERSON, SJ ;
SHERR, CJ .
JOURNAL OF VIROLOGY, 1982, 41 (02) :489-500
[6]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[7]   COMBINED IMMUNOHISTOCHEMICAL STAINING FOR SURFACE IGD AND LYMPHOCYTE-T SUBSETS WITH MONOCLONAL-ANTIBODIES IN HUMAN TONSILS [J].
FELLER, AC ;
PARWARESCH, MR ;
WACKER, HH ;
RADZUN, HJ ;
LENNERT, K .
HISTOCHEMICAL JOURNAL, 1983, 15 (06) :557-562
[8]   HEMOPOIETINS IN ONCOLOGY - FACTORING OUT MYELOSUPPRESSION [J].
GRIFFIN, JD .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (02) :151-155
[9]   MOLECULAR-CLONING OF A COMPLEMENTARY-DNA ENCODING HUMAN MACROPHAGE-SPECIFIC COLONY-STIMULATING FACTOR (CSF-1) [J].
KAWASAKI, ES ;
LADNER, MB ;
WANG, AM ;
VANARSDELL, J ;
WARREN, MK ;
COYNE, MY ;
SCHWEICKART, VL ;
LEE, MT ;
WILSON, KJ ;
BOOSMAN, A ;
STANLEY, ER ;
RALPH, P ;
MARK, DF .
SCIENCE, 1985, 230 (4723) :291-296
[10]  
KREIPE H, 1990, LAB INVEST, V62, P697