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An invertebrate defense molecule activates membrane conductance in mammalian cells by means of its lectin-like domain

  • Alain Bloc
    ,
  • Rudolf Lucas(corresponding author)
    ,
  • Els Van Dijck
    ,
  • Martin Bilej
    ,
  • Yves Dunant
    ,
  • Patrick De Baetselier
*Corresponding author for this work
  • University of Geneva
    ,
  • University of Konstanz
    ,
  • Flanders Institute for Biotechnology
    ,
  • Czech Academy of Sciences
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

The invertebrate defense molecule Coelomic Cytolytic Factor-1 (CCF-1) and the mammalian cytokine Tumor Necrosis Factor (TNF) share a similar lectin-like domain that, upon interaction with specific sugars, causes lysis of African trypanosomes. In contrast to TNF, CCF-1 does not require an acidification of a lysosomal compartment for this activity. Moreover, we could demonstrate using the whole cell patch clamp technique that both TNF and CCF-1 activate amiloride-sensitive channels in mammalian cells, in a TNF receptor-independent way, but, unlike TNF, CCF-1 does not require acidic conditions for this activity. These data confirm the functional analogies of an invertebrate defense molecule and a mammalian cytokine, based on a similar lectin-like interaction.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 35-43 (9 pages)

Journal (Volume, Issue Number)

Developmental and Comparative Immunology (Volume 26, Issue 1)

Publication milestones

  • Published - 2002

Publication status

Published - 2002

ISSN

0145-305X

Publication IDs

  • Scopus: 0036027774
  • PubMed: 11687261

Publication metrics

Metrics

SciVal
FWCI
0.29
SciVal
Author count
7
SciVal
citations
12
SciVal
Paper percentile
61
Fractional count
1
Fractional count
0.14
Fractional count
6
Fractional count
0.86
Fractional count
1
Fractional count
1
Scopus
citations

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Citation count
12
Captures
15

Funding Details

This work was supported by the NATO Collaborative Linkage Grant (LST.CLG974974), the Foundation for Scientific Research-Flanders (G.0169.01), the Grant Agency of the Czech Republic (310/99/1385 and 310/00/1372) and a grant from the Swiss National Foundation for Scientific Research (31.57135.99) and was performed in the frame of an Interuniversity Attraction Pole Program
FundersFunding numbers
Foundation for Scientific Research-Flanders
G.0169.01
Swiss National Foundation for Scientific Research
31.57135.99
NATO
LST.CLG974974
GA ČR
310/00/1372, 310/99/1385