Insulin-like growth factor binding proteins in air- and 85% oxygen-exposed adult rat lung

被引:11
作者
Han, RNN
Han, VKM
Buch, S
Freeman, BA
Post, M
Tanswell, AK
机构
[1] Hosp Sick Children, Div Neonatol, Res Inst, MRC,Grp Lung Dev, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Dept Paediat, Toronto, ON M5S 1A8, Canada
[3] St Josephs Hlth Ctr, Lawson Res Inst, MRC, Grp Fetal & Neonatal Hlth & Dev, London, ON, Canada
[4] Univ Western Ontario, Dept Paediat, London, ON N6A 4V2, Canada
[5] Univ Western Ontario, Dept Anat, London, ON N6A 4V2, Canada
[6] Univ Western Ontario, Dept Biochem, London, ON N6A 4V2, Canada
[7] Univ Alabama, Dept Anesthesiol, Birmingham, AL 35294 USA
[8] Univ Alabama, Dept Biochem, Birmingham, AL 35294 USA
[9] Univ Alabama, Dept Pediat, Birmingham, AL 35294 USA
关键词
pulmonary oxygen toxicity; cell interactions; lung injury;
D O I
10.1152/ajplung.1998.274.4.L647
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Expression of insulin-like growth factor (IGF) I and its type I receptor is increased in the adult rat lung exposed to 85% O-2. We hypothesized that there would be a parallel up-and downregulation of growth-stimulating and growth-inhibiting IGF binding proteins (IGFBPs), respectively. The normal adult rat lung expresses mRNAs for IGFBP-2, -3, -4, -5, and -6 but not for IGFBP-1. O-2 exposure for 6 or 14 days reduced IGFBP-3 and -6 and increased IGFBP-4 mRNA abundance. IGFBP-5 mRNA was reduced at 6 days but increased at 14 days. IGFBP-4 mRNA was localized to perivascular and peribronchial interstitial cells and IGFBP-5 mRNA to airway and alveolar epithelial cells. IGFBP-2, -4, and -5 immunolocalized to airway epithelial cells in normal lung and to perivascular exudates after 6 days in 85% O-2. IGFBP-2 was diffusely increased throughout the lung tissue only after a 6-day exposure. IGFBP-5 was reduced after a 6-day exposure but was increased and widely distributed after 14 days. IGFBP-4 increased over airway epithelium and subepithelial cells after 6 days and over perivascular interstitial cells after 14 days of 85% O-2. These data are consistent with the predicted changes for IGFBPs on O-2 exposure except that the generally growth inhibitory IGFBP-4 was increased at sites of active cell proliferation.
引用
收藏
页码:L647 / L656
页数:10
相关论文
共 43 条
[1]   TISSUE DISTRIBUTION AND REGULATION OF INSULIN-LIKE GROWTH-FACTOR (IGF)-BINDING PROTEIN-3 MESSENGER-RIBONUCLEIC-ACID (MESSENGER-RNA) IN THE RAT - COMPARISON WITH IGF-I MESSENGER-RNA EXPRESSION [J].
ALBISTON, AL ;
HERINGTON, AC .
ENDOCRINOLOGY, 1992, 130 (01) :497-502
[2]  
BALANTYNE JD, 1982, PATHOLOGY OXYGEN TOX, P82
[3]   DEVELOPMENTAL-CHANGES IN THE EXPRESSION PATTERNS OF IGFS, TYPE-1 IGF RECEPTOR AND IGF-BINDING PROTEIN-2 AND PROTEIN-4 IN PERINATAL RAT LUNG [J].
BATCHELOR, DC ;
HUTCHINS, AM ;
KLEMPT, M ;
SKINNER, SJM .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 1995, 15 (02) :105-115
[4]   BASIC FIBROBLAST GROWTH-FACTOR AND GROWTH-FACTOR RECEPTOR GENE-EXPRESSION IN 85-PERCENT O-2-EXPOSED RAT LUNG [J].
BUCH, S ;
HAN, RNN ;
LIU, J ;
MOORE, A ;
EDELSON, JD ;
FREEMAN, BA ;
POST, M ;
TANSWELL, AK .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1995, 268 (03) :L455-L464
[5]  
CAZALS V, 1994, J BIOL CHEM, V269, P14111
[6]   INCREASE IN INSULIN-LIKE GROWTH-FACTOR-I IN HYPERTROPHYING SMOOTH-MUSCLE [J].
CHEN, Y ;
BORNFELDT, KE ;
ARNER, A ;
JENNISCHE, E ;
MALMQVIST, U ;
UVELIUS, B ;
ARNQVIST, HJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (02) :E224-E229
[7]  
CHEN Y, 1995, GROWTH REGULAT, V5, P45
[8]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[9]  
CLEMMONS DR, 1992, GROWTH REGULAT, V2, P80
[10]   A FACTOR CONTAINED IN PLASMA IS REQUIRED FOR IGF BINDING PROTEIN-1 TO POTENTIATE THE EFFECT OF IGF-I ON SMOOTH-MUSCLE CELL-DNA SYNTHESIS [J].
CLEMMONS, DR ;
GARDNER, LI .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 145 (01) :129-135