Human SP-A protein variants derived from one or both genes stimulate TNF-alpha production in the THP-1 cell line

Am J Physiol Lung Cell Mol Physiol. 2000 May;278(5):L946-54. doi: 10.1152/ajplung.2000.278.5.L946.

Abstract

In humans, two functional genes of surfactant protein (SP) A, SP-A1 and SP-A2, and several alleles of each functional gene have been characterized. SP-A is a multimeric molecule consisting of six trimers. Each trimer contains two SP-A1 molecules and one SP-A2 molecule. Until now, it has been unclear whether a single SP-A gene product is functional or whether there are functional differences either among alleles or between single-gene SP-A products and SP-A products derived from both genes. We tested the ability of in vitro expressed SP-A variants to stimulate tumor necrosis factor (TNF)-alpha production by THP-1 cells. We observed that 1) single-gene products and products derived from both genes stimulate TNF-alpha production, 2) there are differences among SP-A1 and SP-A2 alleles in their ability to stimulate TNF-alpha production, and 3) the increases in TNF-alpha production are lower after treatment with the SP-A1 alleles than after treatment with the SP-A2 alleles. Furthermore, coexpressed SP-As from SP-A1 and SP-A2 genes have a higher activity compared with SP-As from individual alleles or mixed SP-As from SP-A1 and SP-A2 genes. These data suggest that the SP-A-induced increases in TNF-alpha levels differ among SP-A variants and appear to be affected by SP-A genotype and whether SP-A is derived from one or both genes.

Publication types

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

MeSH terms

  • Alleles
  • Alternative Splicing / physiology
  • Animals
  • Baculoviridae / genetics
  • Cell Line
  • DNA, Complementary
  • Gene Dosage
  • Gene Expression Regulation, Viral / immunology
  • Humans
  • Lung / cytology*
  • Macrophages, Alveolar / physiology*
  • Proteolipids / chemistry
  • Proteolipids / genetics*
  • Pulmonary Surfactant-Associated Protein A
  • Pulmonary Surfactant-Associated Proteins
  • Pulmonary Surfactants / chemistry
  • Pulmonary Surfactants / genetics*
  • Spodoptera
  • Transfection
  • Tumor Necrosis Factor-alpha / genetics*

Substances

  • DNA, Complementary
  • Proteolipids
  • Pulmonary Surfactant-Associated Protein A
  • Pulmonary Surfactant-Associated Proteins
  • Pulmonary Surfactants
  • SFTPA1 protein, human
  • SFTPA2 protein, human
  • Tumor Necrosis Factor-alpha