4.6 Article

Phylogenetic conservation of the preapoptotic calreticulin exposure pathway from yeast to mammals

期刊

CELL CYCLE
卷 8, 期 4, 页码 639-642

出版社

TAYLOR & FRANCIS INC
DOI: 10.4161/cc.8.4.7794

关键词

calreticulin; ERp57; endoplasmic reticulum stress; caspase; exocytosis

资金

  1. Fonds zur Forderung der wissenschaftlichen Forschung (Austria) [S-9304-B05]
  2. Fonds zur Forderung der wissenschaftlichen Forschung (Austria)
  3. Swedish Research Council (Vetenskapsradet)
  4. Ligue Nationale contre le Cancer (Equipe labellisee)
  5. European Commission
  6. Canceropole Ile-de-France
  7. Fondation de France and Fondation pour la Recherche Medicale
  8. Austrian Science Fund (FWF) [W 901] Funding Source: researchfish

向作者/读者索取更多资源

The pre-apoptotic exposure of calreticulin (CRT) on the cell surface determines the efficient engulfment of mouse or human tumor cells by antigen-presenting dendritic cells. CRT exposure is rapidly induced by anthracyclins and ionizing irradiation and follows a complex signal transduction pathway that is interrupted by depletion of PERK, caspase-8, BAP31, Bax, Bak or SNAREs, as well as by knock-in mutation of eIF2 alpha (to make it non-phosphorylable by PERK) or BAP31 (to render it uncleavable by caspase-8). Here, we show that yeast (Saccharomyces cerevisiae) can expose the CRT orthologue CNE1 on the surface in response to cell death induced by the anthracylin mitoxantrone (MTX). This MTX-triggered CNE1 translocation is abolished by knockout of the yeast orthologues of PERK (Gcn2), BAP31 (Yet3) and SNAREs (Nyv1, Sso1). Altogether, our data point to the existence of an ancestral and cell death-related CRT exposure pathway with conserved elements shared between unicellular fungi and mammals.

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