Insulin-like growth factor-I and type I insulin-like growth factor receptor in 85% O2-exposed rat lung

Robin N.N. Han, Victor K.M. Han, Shilpa J Buch, Bruce A. Freeman, Martin Post, A. Keith Tanswell

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

The expression of insulin-like growth factor I(IGF-I) and insulinlike growth factor II(IGF-II) was studied in the lungs of adult rats exposed to air or 85% O2, using Northern analysis, in situ hybridization, and immunohistochemistry. Distribution of the type I insulin-like growth factor receptor(IGF-IR) was assessed by immunohistochemistry. IGF-I, but not IGF-II, was localized to airway epithelium, while IGF-IK was localized to perivascular and peribronchial cells, in the lungs of animals breathing air. IGF-II mRNA did not increase with exposure to 85% 0%, but IGF-II was localized to sites of perivascular edema and to occasional peribronchial cells. A widespread increase in IGF-I mRNA and peptide was seen after both a 6-day and a 14-day exposure to O2, with maximal expression in the airway and alveolar epithelium, and lesser expression in interstitial cells. After 6 days in 85% O2, increased IGF-IR immunoreactivity was localized to both perivascular and peribronchial cells and to eridothelial cells. By 14 days in 85% O2, IGF-IR immunoreactivity was also localized to alveolar epithelial cells. The distribution of IGF-IR immunoreactivity was consistent with a paracrine role for IGF-I in O2-mediated pulmonary hypertension and airway hyperreactivity, by mediating smooth muscle cell hyperplasia, as well as a role in endothelial cell repair and late pneumocyte hyperplasia. The relative insensitivity of IGF-IR immunohistochemistry did not allow us to identify cells with low abundance IGF-IR, and potential cellular targets for IGF-I actions after O2-exposure may be even more extensive than those recognized here.

Original languageEnglish (US)
JournalAmerican Journal of Physiology
Volume271
Issue number1 PART 1
StatePublished - Dec 1 1996

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IGF Type 1 Receptor
Insulin-Like Growth Factor I
Lung
Intercellular Signaling Peptides and Proteins
Alveolar Epithelial Cells
Immunohistochemistry
Hyperplasia
Epithelium
Air
Messenger RNA
Pulmonary Hypertension
Smooth Muscle Myocytes
In Situ Hybridization
Edema
Respiration
Endothelial Cells
Peptides

Keywords

  • Airway hyperreactivity
  • Cell interactions
  • Lung injury
  • Pulmonary hypertension
  • Pulmonary oxygen toxicity

ASJC Scopus subject areas

  • Physiology (medical)

Cite this

Han, R. N. N., Han, V. K. M., Buch, S. J., Freeman, B. A., Post, M., & Keith Tanswell, A. (1996). Insulin-like growth factor-I and type I insulin-like growth factor receptor in 85% O2-exposed rat lung. American Journal of Physiology, 271(1 PART 1).

Insulin-like growth factor-I and type I insulin-like growth factor receptor in 85% O2-exposed rat lung. / Han, Robin N.N.; Han, Victor K.M.; Buch, Shilpa J; Freeman, Bruce A.; Post, Martin; Keith Tanswell, A.

In: American Journal of Physiology, Vol. 271, No. 1 PART 1, 01.12.1996.

Research output: Contribution to journalArticle

Han, RNN, Han, VKM, Buch, SJ, Freeman, BA, Post, M & Keith Tanswell, A 1996, 'Insulin-like growth factor-I and type I insulin-like growth factor receptor in 85% O2-exposed rat lung', American Journal of Physiology, vol. 271, no. 1 PART 1.
Han, Robin N.N. ; Han, Victor K.M. ; Buch, Shilpa J ; Freeman, Bruce A. ; Post, Martin ; Keith Tanswell, A. / Insulin-like growth factor-I and type I insulin-like growth factor receptor in 85% O2-exposed rat lung. In: American Journal of Physiology. 1996 ; Vol. 271, No. 1 PART 1.
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