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Inhibition of cellular FLICE-like inhibitory protein abolishes insensitivity to interferon-α in a resistant variant of the human U937 cell line

Blomberg, Jeanette (author)
Umeå universitet,Institutionen för medicinsk kemi och biofysik
Höglund, Andreas (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten)
Eriksson, David (author)
Umeå universitet,Immunologi/immunkemi
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Ruuth, Kristina (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten)
Jacobsson, Maria (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten)
Nilsson, Jonas (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten)
Lundgren, Erik (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten)
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 (creator_code:org_t)
2011-05-12
2011
English.
In: Apoptosis (London). - : Springer Science and Business Media LLC. - 1360-8185 .- 1573-675X. ; 16:8, s. 783-794
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Type I interferons constitute a family of pleiotropic cytokines that have a key role in both adaptive and innate immunity. The interferon signalling pathways mediate transcriptional regulation of hundreds of genes, which result in mRNA degradation, decreased protein synthesis, cell cycle inhibition and induction of apoptosis. To elucidate regulatory networks important for interferon induced cell death, we generated interferon resistant U937 cells by selection in progressively increasing concentrations of interferon-α (IFN-α). The results show that IFN-α activates the death receptor signalling pathway and that IFN resistance was associated with cross-resistance to several death receptor ligands in a manner similar to previously described Fas resistant U937 cell lines. Increased expression of the long splice variant of the cellular FLICE-like inhibitor protein (cFLIP-L) was associated with the resistance to death receptor and IFN-α stimulation. Accordingly, inhibition of cFLIP-L expression with cycloheximide or through cFLIP short harpin RNA interference restored sensitivity to Fas and/or IFN-α. Thus, we now show that selection for interferon resistance can generate cells with increased expression of cFLIP, which protects the cells from both IFN-α and death receptor mediated apoptosis.

Subject headings

NATURVETENSKAP  -- Biologi -- Biofysik (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biophysics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)

Keyword

Apoptosis
Death receptor
Resistance
Fas
Interferon
cFLIP

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ref (subject category)
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