Human immunodeficiency virus (HIV-1) cytotoxicity: Perturbation of the cell membrane and depression of phospholipid synthesis

William S. Lynn, Allister Tweedale, Miles W. Cloyd

Research output: Contribution to journalArticle

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Abstract

The molecular mechanism(s) by which human immunodeficiency virus (HIV-1) injures a T-cell line was studied. A pathological role for viral env proteins, which are inserted into the plasma membrane, has been previously demonstrated for HIV as well as other retroviruses which are cytopathic. We therefore initiated studies examining whether perturbations of the cell membrane or membrane-associated biochemical events may be occurring in cells acutely infected with HIV and whether such perturbations, if present, may be responsible for cytopathology. A human T-cell line (ERIC), which is sensitive to the cytopathic effects of HIVs, was infected with HTLV-IIIB and its membrane permeability to cations and its lipid metabolism were studied coincident with the peak expression of viral p24 and with the first sign of cytopathology (slowing of cell division) 72 to 96 hr after infection. It was found that the rate of influx of Ca2+ into the cell increased over that of uninfected cells and that phospholipid synthesis, primarily phosphatidylcholine, became depressed. Diacylglycerol, which serves both as an intermediate for synthesis of phospholipids and as a second-messenger for lymphocyte activation, was also greatly reduced. However, triglyceride synthesis was enhanced, indicating that not all lipid metabolic pathways were being shut down. This decreased membrane-synthetic ability and reduced second-messenger for cell division are likely to be important causes of HIV-1 cytopathology in ERIC cells. This hypothesis was supported by our finding that HIV cytopathology of ERIC cells could be partially prevented by treatment with compounds (diacylglyceride or PMA and transiently by oleic acid) which either replenish diacylglycerol in the infected cell and/or activate protein kinase C or phosphocholine cytidyltransferase, the latter being the rate-limiting step in synthesis of the major structural phospholipid in most cells.

Original languageEnglish (US)
Pages (from-to)43-51
Number of pages9
JournalVirology
Volume163
Issue number1
DOIs
StatePublished - 1988

Fingerprint

HIV-1
Phospholipids
Cell Membrane
HIV
Diglycerides
Second Messenger Systems
Cell Division
Membranes
Choline-Phosphate Cytidylyltransferase
env Gene Products
T-Lymphocytes
Cell Line
Viral Proteins
Retroviridae
Oleic Acid
Lymphocyte Activation
Metabolic Networks and Pathways
Phosphatidylcholines
Lipid Metabolism
Protein Kinase C

ASJC Scopus subject areas

  • Virology
  • Infectious Diseases

Cite this

Human immunodeficiency virus (HIV-1) cytotoxicity : Perturbation of the cell membrane and depression of phospholipid synthesis. / Lynn, William S.; Tweedale, Allister; Cloyd, Miles W.

In: Virology, Vol. 163, No. 1, 1988, p. 43-51.

Research output: Contribution to journalArticle

Lynn, William S. ; Tweedale, Allister ; Cloyd, Miles W. / Human immunodeficiency virus (HIV-1) cytotoxicity : Perturbation of the cell membrane and depression of phospholipid synthesis. In: Virology. 1988 ; Vol. 163, No. 1. pp. 43-51.
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