Spontaneous expression of the c-sis gene and release of a platelet-derived growth factorlike molecule by human alveolar macrophages

J Clin Invest. 1986 Jul;78(1):61-6. doi: 10.1172/JCI112574.

Abstract

Alveolar macrophages from normal individuals and patients with interstitial lung diseases spontaneously expressed a 4.2-kilobase mRNA complementary to the c-sis gene, a proto-oncogene coding for one of the chains of platelet-derived growth factor (PDGF). Concomitantly, these cells released a mediator with the properties of PDGF, including: chemotactic factor for smooth muscle cells whose activity was resistant to heat and acid, but sensitive to reduction; mitogenic (competence) activity for fibroblasts; ability to compete with PDGF for its receptor; and precipitated by an anti-PDGF antibody. While blood monocytes did not contain c-sis mRNA transcripts, monocytes matured in vitro expressed c-sis, consistent with the concept that expression of c-sis occurs during the differentiation of monocytes into alveolar macrophages. Together with the known actions of PDGF, these observations suggest that the c-sis proto-oncogene and its PDGF product are part of the armamentarium available to the alveolar macrophages for normal lung defense and participation in lung inflammation.

MeSH terms

  • Chemotaxis
  • Cycloheximide / pharmacology
  • Gene Expression Regulation*
  • Hot Temperature
  • Humans
  • Hydrogen-Ion Concentration
  • Lung Diseases / genetics
  • Lung Diseases / metabolism*
  • Platelet-Derived Growth Factor / genetics
  • Platelet-Derived Growth Factor / metabolism*
  • Proto-Oncogene Mas
  • Proto-Oncogenes*
  • Pulmonary Alveoli / metabolism*
  • RNA, Messenger / metabolism
  • Radioimmunoassay
  • Transcription, Genetic
  • Trypsin / metabolism

Substances

  • MAS1 protein, human
  • Platelet-Derived Growth Factor
  • Proto-Oncogene Mas
  • RNA, Messenger
  • Cycloheximide
  • Trypsin