HGF receptor associates with the anti-apoptotic protein BAG-1 and prevents cell death

Alberto Bardelli, Paola Longati, Daniela Albero, Sandro Goruppi, Claudio Schneider, Carola Ponzetto, Paolo M. Comoglio

Research output: Contribution to journalArticlepeer-review


The mechanisms by which apoptosis is prevented by survival factors are largely unknown. Using an interaction cloning approach, we identified a protein that binds to the intracellular domain of the hepatocyte growth factor (HGF) receptor. This protein was identified as BAG-1, a recently characterized Bcl-2 functional partner, which prolongs cell survival through unknown mechanisms. Overexpression of BAG-1 in liver progenitor cells enhances protection from apoptosis by HGF. Association of the receptor with BAG-1 occurs in intact cells, is mediated by the C-terminal region of BAG-1 and is independent from tyrosine phosphorylation of the receptor. Formation of the complex is increased rapidly following induction of apoptosis. BAG-1 also enhances platelet-derived growth factor (PDGF)-mediated protection from apoptosis and associates with the PDGF receptor. Microinjection or transient expression of BAG-1 deletion mutants shows that both the N- and the C-terminal domains are required for protection from apoptosis. The finding of a link between growth factor receptors and the anti-apoptotic machinery fills a gap in the understanding of the molecular events regulating programmed cell death.

Original languageEnglish
Pages (from-to)6205-6212
Number of pages8
JournalEMBO Journal
Issue number22
Publication statusPublished - Nov 15 1996


  • Apoptosis
  • BAG-1
  • Bcl-2
  • HGF receptor
  • PDGF receptor

ASJC Scopus subject areas

  • Genetics
  • Cell Biology


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