Fas and Fas-associated death domain protein regulate monocyte chemoattractant protein-1 expression by human smooth muscle cells through caspase- and calpain-dependent release of interleukin-1α

Friedemann J. Schaub, W. Conrad Liles, Nicola Ferri, Kirsten Sayson, Ronald A. Seifert, Daniel F. Bowen-Pope

Research output: Contribution to journalArticlepeer-review

Abstract

We previously reported that treatment of human vascular smooth muscle cells (SMCs) with proapoptotic stimuli, including Fas ligand plus cycloheximide (FasL/Chx), or overexpression of Fas-associated death domain protein (FADD) result in increased expression of monocyte chemoattractant protein-1 (MCP-1) and other proinflammatory genes. In this study, we demonstrate that Fas/FADD-induced MCP-1 upregulation is driven by an autocrine/paracrine signaling loop in which interleukin (IL)-1α synthesis and release are activated through caspase- and calpain-dependent processes. Untreated SMCs contain very little IL-1α protein or transcript. Both were increased greatly in response to Fas/FADD activation, primarily through an autocrine/paracrine pathway in which secreted IL-1α stimulated additional IL-1α synthesis and release. Caspase 8 (Csp8) activity increased in response to FasL/Chx treatment, and Csp8 inhibitors markedly reduced IL-1α release and MCP-1 upregulation. In contrast, Csp8 activity was not significantly increased in response to FADD overexpression and caspase inhibitors did not effect FADD-induced MCP-1 upregulation. Both FasL/Chx treatment and FADD overexpression increased the activity of calpains. Calpain inhibitors reduced IL-1α release and MCP-1 upregulation in both FADD-overexpressing SMCs and FasL/Chx-treated SMCs without blocking Csp8 activity. This indicates that calpains are not required for activation of caspases and that caspase activation is not sufficient for IL-1α release and MCP-1 upregulation. These data suggest that calpains play a dominant role in Fas/FADD-induced IL-la release and MCP-1 upregulation and that caspase activation may function to amplify the effects of calpain activation.

Original languageEnglish
Pages (from-to)515-522
Number of pages8
JournalCirculation Research
Volume93
Issue number6
DOIs
Publication statusPublished - Sep 19 2003

Keywords

  • Apoptosis
  • Calpain
  • Inflammation
  • Interleukin
  • Monocyte chemoattractant protein-1

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

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