A HISTOLOGICALLY DISTINCTIVE INTERSTITIAL PNEUMONIA INDUCED BY OVEREXPRESSION OF THE INTERLEUKIN-6, TRANSFORMING GROWTH-FACTOR-BETA-1, OR PLATELET-DERIVED GROWTH-FACTOR-B GENE
被引:120
作者:
YOSHIDA, M
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机构:OSAKA UNIV,SCH MED,DEPT MED 3,SUITA,OSAKA 565,JAPAN
YOSHIDA, M
SAKUMA, J
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SAKUMA, J
HAYASHI, S
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HAYASHI, S
ABE, K
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ABE, K
SAITO, I
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SAITO, I
HARADA, S
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HARADA, S
SAKATANI, M
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SAKATANI, M
YAMAMOTO, S
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YAMAMOTO, S
MATSUMOTO, N
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MATSUMOTO, N
KANEDA, Y
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KANEDA, Y
KISHIMOTO, T
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KISHIMOTO, T
机构:
[1] OSAKA UNIV,SCH MED,DEPT MED 3,SUITA,OSAKA 565,JAPAN
IN VIVO TRANSFECTION;
HEMAGGLUTINATING VIRUS OF JAPAN-LIPOSOME;
ADENOVIRUS VECTOR;
D O I:
10.1073/pnas.92.21.9570
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Interstitial pneumonia is characterized by alveolitis with resulting fibrosis of the interstitium. To determine the relevance of humoral factors in the pathogenesis of interstitial pneumonia, we introduced expression vectors into Wistar rats via the trachea to locally overexpress humoral factors in the lungs, Human interleukin (IL) 6 and IL-6 receptor genes induced lymphocytic alveolitis without marked fibroblast proliferation. In contrast, overexpression of human transforming growth factor pi or human platelet-derived growth factor B gene induced only mild or apparent cellular infiltration in the alveoli, respectively. However, both factors induced significant proliferation of fibroblasts and deposition of collagen fibrils. These histopathologic changes induced by the transforming growth factor beta 1 and platelet-derived growth factor B gene are partly akin to those changes seen in lung tissues from patients with pulmonary fibrosis and markedly contrast with the changes induced by overexpression of the IL-6 and IL-6 receptor genes that mimics lymphocytic interstitial pneumonia.