Expression of epidermal growth factor and surfactant proteins during postnatal and compensatory lung growth

被引:34
作者
Foster, DJ
Yan, X
Bellotto, DJ
Moe, OW
Hagler, HK
Estrera, AS
Hsia, CCW
机构
[1] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Pathol, Dallas, TX 75390 USA
[3] Univ Texas, SW Med Ctr, Dept Cardiovasc & Thorac Surg, Dallas, TX 75390 USA
[4] Dept Vet Affairs Med Ctr, Med Serv, Dallas, TX 75390 USA
关键词
immunohistochemistry; immunogold; immunoassay; lung resection; pneumonectomy;
D O I
10.1152/ajplung.00053.2002
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We examined whether lung growth after pneumonectomy (PNX) invokes normal signaling pathways of postnatal development. We qualitatively and quantitatively assessed the immunoexpression of epidermal growth factor (EGF), its receptor (EGFR), surfactant proteins (SP) [SP-A and -D and surfactant proproteins (proSP)-B and -C] and proliferating cell nuclear antigen (PCNA) in immature and mature dog lung. We also assayed these proteins in lungs of immature dogs 3 wk or 10 mo after they underwent right PNX compared with simultaneous matched sham controls. During maturation, alveolar cell proliferation is regionally regulated in parallel with EGF and EGFR levels and inversely correlated with SP- A and proSP-C levels. In contrast, post-PNX lung growth is not associated with EGF or EGFR upregulation but with markedly increased SP- A level and moderately increased SP-D level; proSP-B and proSP-C levels did not change. We conclude that 1) signaling of EGF axis and differential regulation of SPs persist during postnatal lung development, 2) post-PNX lung growth is not a simple recapitulation of maturational responses, and 3) SP-A and SP-D may modulate post-PNX lung growth.
引用
收藏
页码:L981 / L990
页数:10
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