Expression of alpha 6 beta 1 integrin, the laminin receptor, on subsets of normal murine lung fibroblasts and its upregulation by the inflammatory cytokines IFN-gamma and TNF-alpha

Reg Immunol. 1992 Nov-Dec;4(6):363-70.

Abstract

The purpose of this investigation was to ascertain whether the alpha 6 integrin subunit was present on normal murine lung cells and fibroblasts, and if so, to determine the identity of the beta subunit coordinately expressed with alpha 6 and whether or not these integrin subunits could be regulated by cytokines. Previously, our laboratory isolated populations of Thy 1+ and Thy 1- fibroblasts from normal murine lung tissue. These cells differed in surface marker expression and in response to, and production of, pro-inflammatory cytokines. Research defining the properties of these two populations has led to the hypothesis that unique groups of fibroblasts exist within the murine lung. Though alpha 6 beta 1 is known to be expressed by platelets, lymphocytes, and epithelial cells, its presence and regulation on lung fibroblast subsets has not been explored. We now report the following findings: 1) the laminin receptor, alpha 6 beta 1, is present on 20-30% of freshly isolated normal murine lung cells in all three murine strains tested; 2) established Thy 1+ and Thy 1- murine lung fibroblast subsets and clones constitutively express alpha 6 beta 1 at varied levels; and 3) alpha 6 beta 1 expression on fibroblast lines and clones can be upregulated by treatment with IFN-gamma or TNF-alpha. Since these T cell and macrophage derived cytokines are known to be present during an inflammatory response, upregulation of alpha 6 beta 1 expression may facilitate recruitment and retention of lung fibroblasts in regions undergoing repair.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antigens, Surface / analysis
  • Base Sequence
  • Cytokines / pharmacology
  • Fibroblasts
  • Gene Expression / drug effects
  • In Vitro Techniques
  • Integrins / metabolism*
  • Interferon-gamma / pharmacology*
  • Lung / cytology
  • Lung / metabolism*
  • Membrane Glycoproteins / analysis
  • Mice
  • Mice, Inbred Strains
  • Molecular Sequence Data
  • Oligodeoxyribonucleotides / chemistry
  • RNA, Messenger / genetics
  • Receptors, Laminin / metabolism*
  • Recombinant Proteins / pharmacology
  • Thy-1 Antigens
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Antigens, Surface
  • Cytokines
  • Integrins
  • Membrane Glycoproteins
  • Oligodeoxyribonucleotides
  • RNA, Messenger
  • Receptors, Laminin
  • Recombinant Proteins
  • Thy-1 Antigens
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma