A human milk factor susceptible to cathepsin D inhibitors enhances human immunodeficiency virus type 1 infectivity and allows virus entry into a mammary epithelial cell line

J Virol. 2000 Jan;74(2):1004-7. doi: 10.1128/jvi.74.2.1004-1007.2000.

Abstract

Human immunodeficiency virus type 1 (HIV-1) growth in lymphocyte cultures was increased when the virus inoculum was incubated in breast milk. The enhancing effect of milk was abolished by anti-cathepsin D antibody or by pepstatin A, a cathepsin D inhibitor. The cathepsin D-producing CD4-negative MCF7 mammary cells supported the growth of some HIV-1 isolates. An MCF7 line chronically producing HIV-1 IIIb was obtained. Cathepsin D may induce conformational modification of viral gp120, allowing direct interaction with a coreceptor. We demonstrated the presence of CXCR4 mRNA in MCF7 cells.

MeSH terms

  • Animals
  • Breast / cytology
  • Breast / virology*
  • Cathepsin D / antagonists & inhibitors
  • Cathepsin D / physiology*
  • Epithelial Cells / virology
  • Female
  • Galactosylceramides / genetics
  • Gene Expression
  • HIV Envelope Protein gp120 / genetics
  • HIV-1 / growth & development*
  • HIV-1 / physiology
  • Humans
  • Milk / enzymology*
  • Pepstatins / pharmacology
  • RNA, Messenger
  • RNA, Viral
  • Receptors, HIV / genetics
  • Tumor Cells, Cultured

Substances

  • Galactosylceramides
  • HIV Envelope Protein gp120
  • Pepstatins
  • RNA, Messenger
  • RNA, Viral
  • Receptors, HIV
  • Streptomyces pepsin inhibitor
  • Cathepsin D
  • pepstatin