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Transplantation. 2000 Aug 27;70(4):656-61.

Inhibition of C-raf expression by antisense oligonucleotides extends heart allograft survival in rats.

Author information

1
Division of Immunology and Organ Transplantation, The University of Texas Medical School at Houston, 77030, USA.

Abstract

BACKGROUND:

C-raf is a well-characterized serine/ threonine (Ser/Thr) protein kinase that is involved in the transduction of multiple signals of T cells. We demonstrate that the inhibition of C-raf mRNA expression prolongs heart allograft survival.

METHODS:

Three 20-mer C-raf antisense oligonucleotides, each with identical sequences, were synthesized with different chemical modifications: one as a uniform phosphorothioate oligodeoxynucleotide (PS oligo), a second with a PS backbone and 2'-methoxyethyl (ME) substitutions at the 2'-sugar positions in the first and last five nucleotides, and a third with a mixed PS and phosphodiester (PD) backbone and ME modifications on the first and last five nucleotides.

RESULTS:

Both ME-modified C-raf antisense oligos were at least 5-fold more effective than the PS C-raf antisense oligo in blocking C-raf mRNA expression in two cell lines. Similarly, each of the ME C-raf antisense oligos produced better heart allograft survival rates than did PS C-raf oligo. Furthermore, although the combination of PS C-raf antisense oligo with sirolimus (SRL) acted synergistically to extend heart allograft survival, the effect was potentiated by either of the ME-modified oligos.

CONCLUSIONS:

C-raf inhibition extends heart allograft survival, and ME-modification potentiates antisense activity.

[Indexed for MEDLINE]

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