Cloning and expression of guinea pig TIMP-2. Expression in normal and hyperoxic lung injury

Am J Physiol Lung Cell Mol Physiol. 2000 Apr;278(4):L737-43. doi: 10.1152/ajplung.2000.278.4.L737.

Abstract

Tissue inhibitors of metalloproteinases (TIMPs) play a key regulatory role in extracellular matrix remodeling. By screening a lung library with a human TIMP-2 cDNA probe, we have isolated the cDNA corresponding to guinea pig TIMP-2. The 3.5-kb cDNA presents an open reading frame that predicts a protein of 220 amino acids showing 97.2, 96.8, 97.2, and 77.3% overall identity with human, mouse, rat, and chicken TIMP-2, respectively. Guinea pig TIMP-2 cDNA was expressed in CHO-K1 cells, showing a protein with the expected molecular weight and activity. Northern blot analysis revealed TIMP-2 expression in brain, kidney, intestine, spleen, heart, and lung. Transforming growth factor-beta downregulated TIMP-2 mRNA in guinea pig lung fibroblasts, whereas a variety of other stimuli showed no effect. In normal and hyperoxia-exposed lungs, TIMP-2 mRNA was mainly localized in alveolar macrophages and epithelial cells. No quantitative differences were found by Northern blot. These results confirm that TIMP-2 is highly conserved in mammals and largely expressed in lungs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence / genetics
  • Animals
  • Base Sequence / genetics
  • Bronchoalveolar Lavage Fluid / chemistry
  • CHO Cells
  • Cloning, Molecular*
  • Cricetinae
  • DNA, Complementary / genetics
  • Fibroblasts / metabolism
  • Gelatinases / analysis
  • Guinea Pigs
  • Hyperoxia / complications*
  • Lung / cytology
  • Lung / metabolism
  • Lung Diseases / etiology*
  • Lung Diseases / metabolism*
  • Male
  • Molecular Sequence Data
  • RNA, Messenger / metabolism
  • Reference Values
  • Tissue Inhibitor of Metalloproteinase-2 / genetics*
  • Tissue Inhibitor of Metalloproteinase-2 / metabolism*

Substances

  • DNA, Complementary
  • RNA, Messenger
  • Tissue Inhibitor of Metalloproteinase-2
  • Gelatinases